Category: 65-22-5

Genotoxicity and biochemical toxicity of soil antibiotics to earthworms was written by Ahmed, Sarfraz;Ibrahim, Muhammad;Waheed, Rashem;Azdee, Abu Bakar Hassan;Hashmi, Muhammad Zaffar;Ahmed, Shabir. And the article was included in Soil Biology in 2017.Recommanded Product: 65-22-5 The following contents are mentioned in the article:

A review. This chapter discusses about the genotoxicity and biochem. toxicity of soil antibiotics to Eisenia fetida and Eudrilus eugeniae in soil ecosystem. This study involved multiple reactions and reactants, such as 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5Recommanded Product: 65-22-5).

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) 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. 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: 65-22-5

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

New Furopyridines Containing Pyridoxal and Pyrazolone Fragments was written by Kibardina, L. K.;Trifonov, A. V.;Burilov, A. R.;Pudovik, M. A.. And the article was included in Russian Journal of General Chemistry in 2018.Application of 65-22-5 The following contents are mentioned in the article:

Reactions of pyridoxal hydrochloride with 5-pyrazolone derivatives in alc. medium in the presence of concentrated hydrochloric acid led to the formation of new pyrazolones with pyridoxal fragments in the mol. The corresponding diarylmethanes were formed when using pyridoxal and pyrazolone in a 1: 2 ratio. This study involved multiple reactions and reactants, such as 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5Application of 65-22-5).

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Application of 65-22-5

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

The novel structural modification of pyridoxal via its cyclization into 2-acyl- and 2-heteroarylfuro[2,3-c]pyridines was written by Morkovnik, Anatolii S.;Zubenko, Alexander A.;Divaeva, Ludmila N.;Kartsev, Victor G.;Borodkin, Gennadii S.;Klimenko, Alexander I.. And the article was included in Mendeleev Communications in 2019.Synthetic Route of C8H10ClNO3 The following contents are mentioned in the article:

A simple method for pyridoxal structural modification via furan ring closure was developed resulting in 2-acyl- and 2-heteroarylfuro[2,3-c]pyridines. The reaction products can be proposed as pyridoxal mimetics to inhibit pyridoxal-5′-phosphate-dependent enzymes. This study involved multiple reactions and reactants, such as 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5Synthetic Route of C8H10ClNO3).

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) 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. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Synthetic Route of C8H10ClNO3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Pyridoxal azomethine salts was written by Bagautdinova, R. H.;Kibardina, L. K.;Pudovik, E. M.;Burilov, A. R.;Pudovik, M. A.. And the article was included in Russian Journal of General Chemistry in 2019.COA of Formula: C8H10ClNO3 The following contents are mentioned in the article:

The reactions of 4-methylpiperazin-1-amine, 2-amino- and 4-aminomethylpiperidines with pyridoxal afforded the corresponding azomethines. Their reactions with organic and inorganic acids lead to the formation of salt derivatives of pyridoxal azomethines. This study involved multiple reactions and reactants, such as 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5COA of Formula: C8H10ClNO3).

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.COA of Formula: C8H10ClNO3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Synthesis of 1-(hydroxyaryl)furo[3,4-c]pyridines from 1-amino(alkoxy)furo[3,4-c]pyridines and (poly)phenols was written by Kibardina, Lyudmila K.;Trifonov, Alexey V.;Dobrynin, Alexey B.;Pudovik, Mikhail A.;Burilov, Alexander R.. And the article was included in Mendeleev Communications in 2018.Quality Control of 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride The following contents are mentioned in the article:

The herein obtained 1-diethylamino-6-methyl-1,3-dihydrofuro[3,4-c]pyridin-7-ol or its 1-ethoxy analog in their reactions with phenols or polyphenols undergo replacement of Et₂N/OEt groups with (poly)hydroxyaryl moieties. This study involved multiple reactions and reactants, such as 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5Quality Control of 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride).

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.Quality Control of 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Enantioselective hyperporous molecularly imprinted thin film polymers was written by Nilsson, Sofia M. E.;Suriyanarayanan, Subramanian;Kathiravan, Subban;Yli-Kauhaluoma, Jari;Kotiaho, Tapio;Nicholls, Ian A.. And the article was included in RSC Advances in 2019.Synthetic Route of C8H10ClNO3 The following contents are mentioned in the article:

Significant enantioselective recognition has been achieved through the introduction of long range ordered and highly interconnected 300 nm diameter pores in molecularly imprinted polymer matrixes. This study involved multiple reactions and reactants, such as 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5Synthetic Route of C8H10ClNO3).

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) 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. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Synthetic Route of C8H10ClNO3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Pyridoxal-derived Schiff’s bases was written by Kibardina, L. K.;Trifonov, A. V.;Pudovik, E. M.;Burilov, A. R.;Pudovik, M. A.. And the article was included in Russian Journal of General Chemistry in 2015.Related Products of 65-22-5 The following contents are mentioned in the article:

In this letter to the editor, the synthesis of pyridoxal derived Schiff bases is presented. The synthesis is predicated on the reaction of pyridoxal with primary amines. This study involved multiple reactions and reactants, such as 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5Related Products of 65-22-5).

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) 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. 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.Related Products of 65-22-5

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Synthesis of Some Derivatives of the 4H-pyrido[4′,3′:5,6]pyrano[2,3-d]pyrimidines was written by Derbisbekova, Uldan B.;Datkhayev, Ubaidilla M.;Kiyekbayeva, Lashyn N.;Zhuravel, Irina A.;Omarova, Roza A.;Turgumbayeva, Aknur A.. And the article was included in Oriental Journal of Chemistry in 2017.Application of 65-22-5 The following contents are mentioned in the article:

Novel method for the synthesis of 4-S-alkylated derivatives of 4H-pyrido[4′,3′:5,6]pyrano[2,3-d]pyrimidine, containing an alkyl- or arylamide moiety has been reported. This study involved multiple reactions and reactants, such as 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5Application of 65-22-5).

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Application of 65-22-5

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Separation characteristics of C30 stationary phase for reverse phase chromatography was written by Nagae, Norikazu;Tsukamoto, Tomoyasu;Koyama, Ryuji. And the article was included in Bunseki in 2021.Application of 65-22-5 The following contents are mentioned in the article:

This paper introduces the separation characteristics of the C30 column, which has a separation selectivity that is significantly different from that of the C18 column. This study involved multiple reactions and reactants, such as 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5Application of 65-22-5).

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. 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 65-22-5

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Utilization of pyridoxal acetal salts as water-triggered, slow-release pro-fragrances was written by Weeks, Kellie L.;Rutkowski, Kyle R.;Morales Loyola, Arnold A.;Boyce, Gregory R.. And the article was included in New Journal of Chemistry in 2018.Category: alcohols-buliding-blocks The following contents are mentioned in the article:

The synthesis of pyridoxal acetal salts and the controlled-release of the alcs. in the presence of neutral pH water is described. The rate of release was monitored by ¹H NMR and was found to be dependent on the concentration of water in the sample. The acetal salts are stable in the absence of moisture and show promise as a vitamin-based pro-fragrance delivery system. This study involved multiple reactions and reactants, such as 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5Category: alcohols-buliding-blocks).

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) 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. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Category: alcohols-buliding-blocks

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts