Category: 106-21-8

Latsky, C. et al. published their research in Journal of Supercritical Fluids in 2018 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Application of 106-21-8

High pressure bubble- and dew-point data for a system containing CO2 with detergent range alkanes and alcohols was written by Latsky, C.;Schwarz, C. E.. And the article was included in Journal of Supercritical Fluids in 2018.Application of 106-21-8 The following contents are mentioned in the article:

The aim of this work was to characterize the solute-solute interactions which exist in the CO2+n-dodecane+3,7-dimethyl-1-octanol +1-decanol system. High pressure bubble- and dew-point data were therefore measured for four different mixtures between 308K and 358K and pressures up to 27.5MPa, with total solute mass fractions ranging between 0.631-0.015. The data were measured using the static synthetic visual phase detection method and experiments were conducted using a high pressure variable volume view cell. The effect of the solute-solute interactions was also analyzed by modeling the phase behavior of the mixtures with the RK-ASPEN model in Aspen Plus. The measured and predicted data indicated that significant solute-solute interactions exist in the quaternary system. The solute-solute interactions were also found to result in complex phase behavior, as mixtures consisting largely of 1-decanol exhibited temperature inversions and co-solvency was found in n-dodecane rich mixtures This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Application of 106-21-8).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Application of 106-21-8

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Meng, Xiangtai et al. published their research in Journal of Organic Chemistry in 2021 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.SDS of cas: 106-21-8

Synthesis of 2-(Cyanomethyl)benzoic Esters via Carbon-Carbon Bond Cleavage of Indanones was written by Meng, Xiangtai;Chen, Dengfeng;Liu, Rui;Jiang, Ping;Huang, Shenlin. And the article was included in Journal of Organic Chemistry in 2021.SDS of cas: 106-21-8 The following contents are mentioned in the article:

A novel synthesis of 2-(cyanomethyl)benzoic esters 2-C(R)CN-3-R1-4-R2-5-R3C6HC(O)OR4 (R = H, Me; R1 = H, Br, CN, CF3; R2 = H, Br, OMe, Cl, etc.; R3 = H, Me, OMe, Br; R4 = Me, Bn, furan-2-ylmethyl, 2H-1,3-benzodioxol-5-ylmethyl, etc.) and ethyl2-(3-cyanopropyl)benzoate from indanone derivatives I (R5 = Me, Ph, 4-trifluoromethylphenyl) and [5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-ylidene]amino acetate has been established. This reaction proceeds via a deprotonation of alcs. R4OH with a chem. base, followed by a nucleophilic addition to indanones I and Beckmann fragmentation. In addition, this reaction could also work under electrochem. conditions, and no external chem. bases were needed. This mild method offers a novel strategy for the late-stage functionalization of various natural alcs. such as citronellol, nerol, abietyl alc., etc. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8SDS of cas: 106-21-8).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.SDS of cas: 106-21-8

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Song, Fei et al. published their research in Journal of Vinyl and Additive Technology in 2020 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.SDS of cas: 106-21-8

Rosin-derived poly(vinyl chloride) plasticizer: Synthesis, structure, and properties was written by Song, Fei;Jia, Puyou;Xia, Haoyu;Zhang, Meng;Hu, Lihong;Zhou, Yonghong. And the article was included in Journal of Vinyl and Additive Technology in 2020.SDS of cas: 106-21-8 The following contents are mentioned in the article:

In this work, rosin-based plasticizer was synthesized by Diels-Alder (DA) and esterification. First, the maleopimaric acid (RT) was obtained by DA between the double bond of rosin and maleic anhydride. Then, the carboxyl group and anhydride group of RT was esterified with tetrahydro geraniol to obtain the rosin-based polyacid esters (RTT) under the catalysis of p-toluene sulfonic acid. The structure of RT and RTT was detected by FTIR and 1H-NMR. RTT was used as main plasticizer to obtain plasticized polyvinyl chloride (PVC) materials and compared with DOP. The results showed that RTT improved the thermal stability and reduced Tg of PVC film. Plasticized PVC films had excellent mech. properties with the elastic modulus of -4,793.67 MPa and tensile strength of -111.86 MPa, higher than that of pure PVC and DOP-6. RTT showed better volatility stability, migration, and solvent extraction in PVC compared to DOP. J. VINYL ADDIT. TECHNOL., 2019. © 2019 Society of Plastics Engineers. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8SDS of cas: 106-21-8).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.SDS of cas: 106-21-8

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Belhassan, A. et al. published their research in Materials Today: Proceedings in 2019 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Recommanded Product: 3,7-Dimethyloctan-1-ol

QSPR Study of the Retention/Release Property of Odorant Molecules in Water, Dairy and Pectin gels was written by Belhassan, A.;Chtita, S.;Lakhlifi, T.;Bouachrine, M.. And the article was included in Materials Today: Proceedings in 2019.Recommanded Product: 3,7-Dimethyloctan-1-ol The following contents are mentioned in the article:

As continuation of our research work on the development and prediction of retention/release property of odorant mols. in Water and pectin gels, in this research, on the one hand, we investigate to establish the quant. structure property relationship (QSPR) of the retention/release property of odorant mols. in dairy gels using principal components anal. (PCA) and multiple linear regression (MLR). We propose quant. models according to these analyses. The multiple linear regression (MLR) method showed a correlation coefficient of 0.901 and 0.917 for DG (dairy gel without pectin) and DG-P (dairy gel with pectin) medias, resp. On the other hand, we compared these results with the other of our previous works to detect the pectin impacts of the retention/release property of studied compounds in different medias (with and without pectin). The comparison indicates that the effects of pectin vary according mols.: adding pectin increases the retention of some mols., but increases the release of other mols. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Recommanded Product: 3,7-Dimethyloctan-1-ol).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Recommanded Product: 3,7-Dimethyloctan-1-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Baptista, Ines et al. published their research in International Journal of Biochemistry & Cell Biology in 2019 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Recommanded Product: 3,7-Dimethyloctan-1-ol

A comprehensive look into the volatile exometabolome of enteroxic and non-enterotoxic Staphylococcus aureus strains was written by Baptista, Ines;Santos, Magda;Rudnitskaya, Alisa;Saraiva, Jorge A.;Almeida, Adelaide;Rocha, Silvia M.. And the article was included in International Journal of Biochemistry & Cell Biology in 2019.Recommanded Product: 3,7-Dimethyloctan-1-ol The following contents are mentioned in the article:

Staphylococcal food poisoning is a disease that originates significant health and economic losses and is caused by Staphylococcus aureus strains able to produce enterotoxins. The aim of this work is to go further on the study of the volatile exometabolome of S. aureus using an advanced gas chromatog. technique. Enterotoxic and non-enterotoxic strains were assessed. The volatile exometabolome profile comprised 240 volatiles belonging to ten chem. families. This volatiles were mainly byproducts of branched-chain amino acids and methionine degradation, pyruvate metabolism, diacetyl pathway, oxidative stress and carotenoid cleavage. Metabolites released by the first two pathways were produced in higher contents by the enterotoxic strains. This study add further insights to S. aureus volatile exometabolome, and also shows that by applying it, it is possible to distinguish strains of S. aureus by the number of produced enterotoxins, which is especially important from the food safety point of view. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Recommanded Product: 3,7-Dimethyloctan-1-ol).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Recommanded Product: 3,7-Dimethyloctan-1-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Xu, Lin et al. published their research in Renewable Energy in 2019 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Application In Synthesis of 3,7-Dimethyloctan-1-ol

Production of bio-fuel oil from pyrolysis of plant acidified oil was written by Xu, Lin;Cheng, Jin-Hong;Liu, Peng;Wang, Qian;Xu, Zhi-Xiang;Liu, Qing;Shen, Jin-You;Wang, Lian-Jun. And the article was included in Renewable Energy in 2019.Application In Synthesis of 3,7-Dimethyloctan-1-ol The following contents are mentioned in the article:

This study investigated the pyrolysis of plant acidified oil, aiming to upgrade the quality of oil for fuel use. The decomposition temperature of plant acidified oil was in the range of 300 oC-500 °C in 10 K/min according to TG-DTG. The Py-GC-MS results showed that except alkane, alkene and oxygen containing compound, plant sterol derivatives were also detected. The ESI FT-ICR MS results showed the presence of some products produced from hydrogenation and polymerization reaction occurred in pyrolysis process. The yield of the liquid product reached the maximum of 90% at 500 °C. The acid value and viscosity of pyrolysis products were relative high compared with diesel oil. The calorific value has no difference with that of diesel oil. According to above experiments, it was confirmed that pyrolysis components and characteristic of plant acidified oil was different with vegetable oil or fatty acid. Plant acidified oil was potential renewable source to obtain bio-fuel oil using pyrolysis method. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Application In Synthesis of 3,7-Dimethyloctan-1-ol).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Application In Synthesis of 3,7-Dimethyloctan-1-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Dupeux, Tristan et al. published their research in Flavour and Fragrance Journal in 2022 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Reference of 106-21-8

COSMO-RS as an effective tool for predicting the physicochemical properties of fragrance raw materials was written by Dupeux, Tristan;Gaudin, Theophile;Marteau-Roussy, Clementine;Aubry, Jean-Marie;Nardello-Rataj, Veronique. And the article was included in Flavour and Fragrance Journal in 2022.Reference of 106-21-8 The following contents are mentioned in the article:

A predictive tool called COSMO-RS, Conductor-Like Screening Model for Real Solvents, based on quantum chem., dielec. continuum models, electrostatics surface interactions, and statistical thermodn., has been used to predict five key physicochem. properties of raw materials used in perfumery industries. The prediction of b.p. (BP), octanol-water partition coefficient (log P), vapor pressure (VP), water solubility (WS), and Henry′s law constant (HLC) of fragrance mols. has been validated with a reference data set of 166 organic compounds Knowing these properties for a fragrance mol. is essential and being able to predict them precisely can be particularly useful in the development of new mols. or in the replacement of controversial mols. regarding safety issues without compromising the overall hedonic accord. Finally, mapping the vapor pressure vs. the Henry′s law constant and the octanol-water partition coefficient consistently predicts the note class of the mols. useful for release comparison of captives. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Reference of 106-21-8).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Reference of 106-21-8

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Latsky, C. et al. published their research in Journal of Supercritical Fluids in 2018 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Application of 106-21-8

High pressure bubble- and dew-point data for a system containing CO2 with detergent range alkanes and alcohols was written by Latsky, C.;Schwarz, C. E.. And the article was included in Journal of Supercritical Fluids in 2018.Application of 106-21-8 The following contents are mentioned in the article:

The aim of this work was to characterize the solute-solute interactions which exist in the CO2+n-dodecane+3,7-dimethyl-1-octanol +1-decanol system. High pressure bubble- and dew-point data were therefore measured for four different mixtures between 308K and 358K and pressures up to 27.5MPa, with total solute mass fractions ranging between 0.631-0.015. The data were measured using the static synthetic visual phase detection method and experiments were conducted using a high pressure variable volume view cell. The effect of the solute-solute interactions was also analyzed by modeling the phase behavior of the mixtures with the RK-ASPEN model in Aspen Plus. The measured and predicted data indicated that significant solute-solute interactions exist in the quaternary system. The solute-solute interactions were also found to result in complex phase behavior, as mixtures consisting largely of 1-decanol exhibited temperature inversions and co-solvency was found in n-dodecane rich mixtures This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Application of 106-21-8).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Application of 106-21-8

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Meng, Xiangtai et al. published their research in Journal of Organic Chemistry in 2021 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.SDS of cas: 106-21-8

Synthesis of 2-(Cyanomethyl)benzoic Esters via Carbon-Carbon Bond Cleavage of Indanones was written by Meng, Xiangtai;Chen, Dengfeng;Liu, Rui;Jiang, Ping;Huang, Shenlin. And the article was included in Journal of Organic Chemistry in 2021.SDS of cas: 106-21-8 The following contents are mentioned in the article:

A novel synthesis of 2-(cyanomethyl)benzoic esters 2-C(R)CN-3-R1-4-R2-5-R3C6HC(O)OR4 (R = H, Me; R1 = H, Br, CN, CF3; R2 = H, Br, OMe, Cl, etc.; R3 = H, Me, OMe, Br; R4 = Me, Bn, furan-2-ylmethyl, 2H-1,3-benzodioxol-5-ylmethyl, etc.) and ethyl2-(3-cyanopropyl)benzoate from indanone derivatives I (R5 = Me, Ph, 4-trifluoromethylphenyl) and [5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulen-6-ylidene]amino acetate has been established. This reaction proceeds via a deprotonation of alcs. R4OH with a chem. base, followed by a nucleophilic addition to indanones I and Beckmann fragmentation. In addition, this reaction could also work under electrochem. conditions, and no external chem. bases were needed. This mild method offers a novel strategy for the late-stage functionalization of various natural alcs. such as citronellol, nerol, abietyl alc., etc. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8SDS of cas: 106-21-8).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.SDS of cas: 106-21-8

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Song, Fei et al. published their research in Journal of Vinyl and Additive Technology in 2020 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.SDS of cas: 106-21-8

Rosin-derived poly(vinyl chloride) plasticizer: Synthesis, structure, and properties was written by Song, Fei;Jia, Puyou;Xia, Haoyu;Zhang, Meng;Hu, Lihong;Zhou, Yonghong. And the article was included in Journal of Vinyl and Additive Technology in 2020.SDS of cas: 106-21-8 The following contents are mentioned in the article:

In this work, rosin-based plasticizer was synthesized by Diels-Alder (DA) and esterification. First, the maleopimaric acid (RT) was obtained by DA between the double bond of rosin and maleic anhydride. Then, the carboxyl group and anhydride group of RT was esterified with tetrahydro geraniol to obtain the rosin-based polyacid esters (RTT) under the catalysis of p-toluene sulfonic acid. The structure of RT and RTT was detected by FTIR and 1H-NMR. RTT was used as main plasticizer to obtain plasticized polyvinyl chloride (PVC) materials and compared with DOP. The results showed that RTT improved the thermal stability and reduced Tg of PVC film. Plasticized PVC films had excellent mech. properties with the elastic modulus of -4,793.67 MPa and tensile strength of -111.86 MPa, higher than that of pure PVC and DOP-6. RTT showed better volatility stability, migration, and solvent extraction in PVC compared to DOP. J. VINYL ADDIT. TECHNOL., 2019. © 2019 Society of Plastics Engineers. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8SDS of cas: 106-21-8).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.SDS of cas: 106-21-8

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts