CAS 55289-05-9

Benzoic acid, 3-hydroxy-2-methyl-, methyl ester

Description:

Benzoic acid, 3-hydroxy-2-methyl-, methyl ester, also known by its CAS number 55289-05-9, is an organic compound that belongs to the class of benzoic acid derivatives. This compound features a benzoic acid core with a hydroxyl group and a methyl group at the 3 and 2 positions, respectively, and a methyl ester functional group. It is typically a colorless to pale yellow liquid with a characteristic aromatic odor. The presence of the hydroxyl group contributes to its solubility in polar solvents, while the ester group influences its reactivity and potential applications. This compound is often used in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals, fragrances, and agrochemicals. Its properties include moderate volatility and stability under standard conditions, although it may undergo hydrolysis in the presence of strong acids or bases. Safety data should be consulted for handling and exposure guidelines, as with all chemical substances.

Formula: C₉H₁₀O₃

Synonyms:

• Methyl 3-Hydroxy-2-Methylbenzoate

Methyl 3-hydroxy-2-methylbenzoate

CAS: 55289-05-9

Formula: C₉H₁₀O₃

Purity: 97%

Color and Shape: Solid

Molecular weight: 166.1739

Ref: IN-DA00DKVK

Methyl 3-hydroxy-2-methylbenzoate

CAS: 55289-05-9

Methyl 3-hydroxy-2-methylbenzoate

Purity: 98%

Molecular weight: 166.17g/mol

Ref: 54-OR912132

Methyl 3-hydroxy-2-methylbenzoate

CAS: 55289-05-9

Methyl 3-hydroxy-2-methylbenzoate is a metabolite that is created when methyl 3-hydroxybenzoate is irradiated with UV light. It can be used as a reagent in Wittig reactions and can be brominated to produce bromoethyl 3-hydroxy-2-methylbenzoate. Methyl 3-hydroxy-2-methylbenzoate is also an intermediate in the acetylation of phenols and the organometallic demethylation of methyltetrahydrofolate.
Methyl 3-hydroxybenzoate reacts with chlorides to produce methyl 2,3,4,5,6-pentahydroxybenzoate. This reaction is catalyzed by Streptomyces species. This compound can be converted into other compounds through various reactions including the wittig reaction and hydrolysis with amines such as ethanolamine or isopropylamine.

Formula: C₉H₁₀O₃

Purity: Min. 95%

Color and Shape: White Powder

Molecular weight: 166.17 g/mol

Ref: 3D-FM70021

METHYL 3-HYDROXY-2-METHYLBENZOATE

CAS: 55289-05-9

Formula: C₉H₁₀O₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 166.176

Ref: 10-F474861