Category: 60549-26-0

Dickschat, Jeroen S. et al. published their research in Beilstein Journal of Organic Chemistry in 2018 | CAS: 60549-26-0

3-Hydroxy-5-methylbenzaldehyde (cas: 60549-26-0) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. 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.COA of Formula: C8H8O2

Volatiles from the xylarialean fungus Hypoxylon invadens was written by Dickschat, Jeroen S.;Wang, Tao;Stadler, Marc. And the article was included in Beilstein Journal of Organic Chemistry in 2018.COA of Formula: C8H8O2 This article mentions the following:

The volatiles emitted by agar plate cultures of the xylarialean fungus Hypoxylon invadens were investigated by use of a closed loop stripping apparatus in combination with GC-MS. Several aromatic compounds were found that could only be identified by comparison to all possible constitutional isomers with different ring substitution patterns. For the set of identified compounds a plausible biosynthetic scheme was suggested that gives further support for the assigned structures. In the experiment, the researchers used many compounds, for example, 3-Hydroxy-5-methylbenzaldehyde (cas: 60549-26-0COA of Formula: C8H8O2).

3-Hydroxy-5-methylbenzaldehyde (cas: 60549-26-0) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. 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.COA of Formula: C8H8O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Dickschat, Jeroen S. et al. published their research in Beilstein Journal of Organic Chemistry in 2018 | CAS: 60549-26-0

3-Hydroxy-5-methylbenzaldehyde (cas: 60549-26-0) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. 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.COA of Formula: C8H8O2

Volatiles from the xylarialean fungus Hypoxylon invadens was written by Dickschat, Jeroen S.;Wang, Tao;Stadler, Marc. And the article was included in Beilstein Journal of Organic Chemistry in 2018.COA of Formula: C8H8O2 This article mentions the following:

The volatiles emitted by agar plate cultures of the xylarialean fungus Hypoxylon invadens were investigated by use of a closed loop stripping apparatus in combination with GC-MS. Several aromatic compounds were found that could only be identified by comparison to all possible constitutional isomers with different ring substitution patterns. For the set of identified compounds a plausible biosynthetic scheme was suggested that gives further support for the assigned structures. In the experiment, the researchers used many compounds, for example, 3-Hydroxy-5-methylbenzaldehyde (cas: 60549-26-0COA of Formula: C8H8O2).

3-Hydroxy-5-methylbenzaldehyde (cas: 60549-26-0) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. 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.COA of Formula: C8H8O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Wu, Liqiang et al. published their research in European Journal of Medicinal Chemistry in 2020 | CAS: 60549-26-0

3-Hydroxy-5-methylbenzaldehyde (cas: 60549-26-0) 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. 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-Hydroxy-5-methylbenzaldehyde

Synthesis and biological evaluation of β-lapachone-monastrol hybrids as potential anticancer agents was written by Wu, Liqiang;Ma, Xin;Yang, Xiaojuan;Zhang, Chong. And the article was included in European Journal of Medicinal Chemistry in 2020.Recommanded Product: 3-Hydroxy-5-methylbenzaldehyde This article mentions the following:

A series of novel β-lapachone analogs I (R1 = H, 10-Br, 8-MeO, etc., R2 = H, 4-Cl, 6-F, 5-Me, etc.) was designed and synthesized by replacing the pyran ring of β-lapachone with the tetrahydropyrimidinethione moiety of monastrol. These hybrids had potent antiproliferative activity against NQO1-rich cell lines (HepG2 and A549; NQO1 = NAD(P)H:quinone oxidoreductase-1), while NQO1-deficient cell lines (H596 and LO2) were less sensitive to these hybrids. Dicoumarol partially inhibited the activity of these compounds against A549 cell lines, indicating that the activation of biol. reduction mediated by NQO1 might partly affect the antiproliferative effects. The NQO1 assay and docking study demonstrated that I (R1 = 8-MeO, R2 = H) (II) was a good substrate of NQO1. Furthermore, as suggested by cellular mechanistic research concerning antitumor activity, the representative compound II resulted in ROS production depending on NQO1, then oxidative stress-triggered apoptotic cell death. Importantly, II significantly suppressed cancer growth in HepG2 xenograft models without obvious toxicity, suggesting that II deserve further research as potent antitumor agents for cancer therapy. In the experiment, the researchers used many compounds, for example, 3-Hydroxy-5-methylbenzaldehyde (cas: 60549-26-0Recommanded Product: 3-Hydroxy-5-methylbenzaldehyde).

3-Hydroxy-5-methylbenzaldehyde (cas: 60549-26-0) 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. 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-Hydroxy-5-methylbenzaldehyde

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts