CAS 52784-32-4

Cycloheptanecarboxylic acid, 2-oxo-, methyl ester

Description:

Cycloheptanecarboxylic acid, 2-oxo-, methyl ester, with the CAS number 52784-32-4, is an organic compound characterized by its cyclic structure and functional groups. It features a cycloheptane ring, which is a seven-membered carbon ring, and contains a carboxylic acid group that has been esterified with methanol, resulting in a methyl ester. The presence of a ketone (2-oxo) group indicates that there is a carbonyl group (C=O) adjacent to the carboxylic acid moiety. This compound is likely to be a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is expected to be soluble in organic solvents due to its ester functionality, while its carboxylic acid nature may impart some degree of polarity. Cycloheptanecarboxylic acid derivatives are of interest in various fields, including organic synthesis and medicinal chemistry, due to their potential biological activities and applications in the development of pharmaceuticals and agrochemicals.

Formula: C₉H₁₄O₃

InChI: InChI=1S/C9H14O3/c1-12-9(11)7-5-3-2-4-6-8(7)10/h7H,2-6H2,1H3

InChI key: InChIKey=BLNHITXSJKCQGZ-UHFFFAOYSA-N

SMILES: C(OC)(=O)C1C(=O)CCCCC1

Synonyms:

• 2-(Methoxycarbonyl)cycloheptanone
• 2-Oxocycloheptanecarboxylic acid methyl ester
• Cycloheptanecarboxylic acid, 2-oxo-, methyl ester
• Ethyl 2-Oxocycloheptanecarboxylate
• Methyl 2-Oxocycloheptanecarboxylate
• NSC 148967

Methyl 2-oxo-cycloheptanecarboxylate

CAS: 52784-32-4

Formula: C₉H₁₄O₃

Purity: 97%

Color and Shape: Liquid

Molecular weight: 170.2057

Ref: IN-DA003ROZ

Methyl 2-oxo-1-cycloheptanecarboxylate

CAS: 52784-32-4

Methyl 2-oxo-1-cycloheptanecarboxylate

Purity: 97%

Molecular weight: 170.21g/mol

Ref: 54-OR322377

Methyl 2-oxo-cycloheptanecarboxylate

CAS: 52784-32-4

Formula: C₉H₁₄O₃

Purity: 95%

Color and Shape: Liquid

Molecular weight: 170.208

Ref: 10-F228000

Methyl 2-oxo-1-cycloheptanecarboxylate

CAS: 52784-32-4

Methyl 2-oxo-1-cycloheptanecarboxylate is a quinoline derivative that inhibits the activity of sirtuin 2 enzyme. It has been shown to inhibit cancer cells in vitro and in vivo, as well as to induce apoptosis. This drug also inhibits the growth of human leukemia cells by inhibiting protein synthesis, which may be due to its ability to activate hydroxy groups in proteins. Methyl 2-oxo-1-cycloheptanecarboxylate is an activated form that can be synthesized from cyclohexanol and transfer reactions with amidines or alkoxycarbonyls. The carbonyl group on this compound is metabolized into carbon dioxide, water, and energy via oxidative reactions with glutathione peroxidase.

Formula: C₉H₁₄O₃

Purity: Min. 95%

Molecular weight: 170.21 g/mol

Ref: 3D-CCA78432