CAS 55211-85-3
:Benzoic acid, 2-hydroxy-3-methyl-, ethyl ester
Description:
Benzoic acid, 2-hydroxy-3-methyl-, ethyl ester, commonly known as ethyl 2-hydroxy-3-methylbenzoate, is an organic compound characterized by its ester functional group derived from benzoic acid. It features a hydroxyl group (-OH) and a methyl group (-CH3) attached to the benzene ring, contributing to its unique properties. This compound typically appears as a colorless to pale yellow liquid with a pleasant, fruity odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic aromatic structure. Ethyl 2-hydroxy-3-methylbenzoate is often used in the fragrance and flavor industry, as well as in the synthesis of other chemical compounds. Its chemical stability and relatively low toxicity make it suitable for various applications, although safety precautions should be observed during handling. As with many esters, it can undergo hydrolysis in the presence of water and acids or bases, reverting to its parent acid and alcohol.
Formula:C10H12O3
InChI:InChI=1S/C10H12O3/c1-3-13-10(12)8-6-4-5-7(2)9(8)11/h4-6,11H,3H2,1-2H3
InChI key:InChIKey=NSRLIMVWJNHWJW-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1=C(O)C(C)=CC=C1
Synonyms:- Benzoic Acid, 2-Hydroxy-3-Methyl-, Ethyl Ester
- Ethyl 3-methylsalicylate
- NSC 97235
- Ethyl 2-hydroxy-3-methylbenzoate
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Found 3 products.
Ethyl 2-hydroxy-3-methylbenzoate
CAS:<p>Ethyl 2-hydroxy-3-methylbenzoate is an organic compound with the chemical formula CH3COCH2CH(OH)COOH. It is a colorless liquid that is soluble in alcohol, ether, and chloroform. It has been used as a precursor to salicylic acid and other compounds with similar function. This product can be synthesized by cyclization of enol ethers with acid derivatives or by cyclization of alkyl phenols with anhydrides. Cyclization reactions are efficient, requiring only a few steps and high temperatures. Salicylic acid can also be obtained from ethyl 2-hydroxy-3-methylbenzoate via hydrolysis of the ester group, which then undergoes decarboxylation to form salicylic acid.</p>Formula:C10H12O3Purity:Min. 95%Molecular weight:180.2 g/mol


