CAS 3955-29-1
:1,2,3-Benzenetriol, 4-methyl-
Description:
1,2,3-Benzenetriol, 4-methyl- is an organic compound characterized by a benzene ring substituted with three hydroxyl (–OH) groups and a methyl (–CH3) group. This compound is part of the phenolic family, which is known for its aromatic properties and the presence of multiple hydroxyl groups that can influence its reactivity and solubility. The presence of three hydroxyl groups makes it a triol, which can participate in hydrogen bonding, enhancing its solubility in polar solvents. The methyl group introduces additional steric effects and can influence the compound's overall reactivity and interaction with other molecules. 1,2,3-Benzenetriol, 4-methyl- may exhibit antioxidant properties due to the presence of hydroxyl groups, which can donate hydrogen atoms to free radicals. Its applications may extend to fields such as pharmaceuticals, where it could serve as an intermediate or active ingredient, and in materials science for the development of phenolic resins. As with many organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.
Formula:C7H8O3
InChI:InChI=1S/C7H8O3/c1-4-2-3-5(8)7(10)6(4)9/h2-3,8-10H,1H3
InChI key:InChIKey=PHZREHARUPHHCU-UHFFFAOYSA-N
SMILES:OC1=C(O)C(O)=CC=C1C
Synonyms:- 2,3,4-Trihydroxy toluene
- 4-Methyl-1,2,3-benzenetriol
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Found 3 products.
4-Methylpyrogallol
CAS:<p>Applications 4-Methylpyrogallol can be used to develop lignophenol derivatives as enzyme inhibitors and novel compounds that targets the GPR35-hERG signalling complex for treating inflammation, metabolic disorder, inflammatory bowel disorder, congestive heart failure, or cancer.<br>References Deng, H., et al. : U.S. Pat. Appl. Publ. US 20130316985 A1 20131128 (2013); Uyama, H., et al.: Jpn. Kokai Tokkyo Koho JP 2007291034 A 20071108 (2007)<br></p>Formula:C7H8O3Color and Shape:Off White SolidMolecular weight:140.137
