CAS 2785-75-3
:3,5-Dimethyl-1,2-benzenediol
Description:
3,5-Dimethyl-1,2-benzenediol, also known as 3,5-dimethyl catechol, is an organic compound characterized by its aromatic structure featuring two hydroxyl (-OH) groups and two methyl (-CH₃) groups attached to a benzene ring. This compound is a derivative of catechol, with the methyl groups positioned at the 3 and 5 positions relative to the hydroxyl groups. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of hydroxyl groups imparts polar characteristics, making it soluble in water and various organic solvents. 3,5-Dimethyl-1,2-benzenediol exhibits antioxidant properties and can participate in various chemical reactions, including oxidation and substitution reactions. It is used in organic synthesis and may serve as an intermediate in the production of dyes, pharmaceuticals, and other chemical compounds. Safety data indicates that it should be handled with care, as it may cause irritation upon contact with skin or eyes.
Formula:C8H10O2
InChI:InChI=1/C8H10O2/c1-5-3-6(2)8(10)7(9)4-5/h3-4,9-10H,1-2H3
InChI key:InChIKey=YGLVLWAMIJMBPF-UHFFFAOYSA-N
SMILES:OC1=C(C)C=C(C)C=C1O
Synonyms:- 3,5-Dimethylpyrocatechol
- 1,2-benzenediol, 3,5-dimethyl-
- Pyrocatechol, 3,5-dimethyl-
- 3,5-DIMETHYL-1,2-BENZENEDIOL
- 3,5-Dimethylbenzene-1,2-diol
- 1,2-Benzenediol, 3,5-dimethyl-
- 3,5-Dimethyl-1,2-benzenediol
- 3,5-Dimethylcatechol
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Found 2 products.
3,5-Dimethylbenzene-1,2-diol
CAS:3,5-Dimethylbenzene-1,2-diol is a chemical compound that belongs to the class of organic compounds. This molecule can be synthesised from 3,5-dimethylbenzoic acid. The oxidation of this molecule was achieved by using an intramolecular reaction with potassium permanganate. The configuration of the molecules are in a cis form. This molecule is used as an intermediate for various other organic compounds such as carbohydrates and antibiotics. 3,5-Dimethylbenzene-1,2-diol can be isolated from natural sources such as plants or fungi. The chemical synthesis of this molecule requires a Diels–Alder reaction between two cyclohexadiene rings and three methyl groups.Formula:C8H10O2Purity:Min. 95%Molecular weight:138.16 g/mol

