CAS 5396-14-5

ethyl oxo(2-oxocyclohexyl)acetate

Description:

Ethyl oxo(2-oxocyclohexyl)acetate, with the CAS number 5396-14-5, is an organic compound characterized by its ester functional group. It features a cyclohexyl ring that is substituted with a ketone group, contributing to its reactivity and potential applications in organic synthesis. The presence of the ethyl acetate moiety suggests that it can participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. This compound is typically a colorless to pale yellow liquid with a pleasant odor, making it suitable for use in flavor and fragrance formulations. Its solubility in organic solvents, combined with its relatively low volatility, allows for diverse applications in chemical synthesis and as an intermediate in the production of other chemical compounds. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if inhaled or ingested. Overall, ethyl oxo(2-oxocyclohexyl)acetate is a versatile compound with potential utility in various fields of chemistry.

Formula: C₁₀H₁₄O₄

InChI: InChI=1/C10H14O4/c1-2-14-10(13)9(12)7-5-3-4-6-8(7)11/h7H,2-6H2,1H3

SMILES: CCOC(=O)C(=O)C1CCCCC1=O

Synonyms:

• Cyclohexaneacetic Acid, Alpha,2-Dioxo-, Ethyl Ester
• Ethyl 2-Oxo-2-(2-Oxocyclohexyl)Acetate
• Ethyl oxo(2-oxocyclohexyl)acetate

2-Oxocyclohexaneglyoxylic acid ethyl ester

CAS: 5396-14-5

Formula: C₁₀H₁₄O₄

Purity: 95%

Color and Shape: Liquid

Molecular weight: 198.2158

Ref: IN-DA00DB0Y

Ethyl 2-oxo-2-(2-oxocyclohexyl)acetate

CAS: 5396-14-5

Ethyl 2-oxo-2-(2-oxocyclohexyl)acetate

Purity: 95%

Molecular weight: 198.22g/mol

Ref: 54-OR1002568

2-Oxocyclohexaneglyoxylic acid ethyl ester

CAS: 5396-14-5

Formula: C₁₀H₁₄O₄

Purity: 95%

Molecular weight: 198.218

Ref: 10-F433394

Ethyl oxo(2-oxocyclohexyl)acetate

CAS: 5396-14-5

Ethyl oxo(2-oxocyclohexyl)acetate is a condensation product of glycine and anhydride, which is obtained by heating the two components in the presence of acid. The reaction yields an isomeric mixture of ethyl oxo(2-oxocyclohexyl)acetate and ethyl oxo(3-oxocyclohexyl)acetate. The condensation products are hydrolyzed to their respective amino acids with ammonia or sodium hydroxide. Ethyl oxo(2-oxocyclohexyl)acetate can also be synthesized from glycine ethyl ester and aminomalonic acid in the presence of enamine.

Formula: C₁₀H₁₄O₄

Purity: Min. 95%

Molecular weight: 198.22 g/mol

Ref: 3D-FAA39614