CAS 57964-61-1

Cyclopentanecarboxylic acid, 3-methyl-2-oxo-, methyl ester

Description:

Cyclopentanecarboxylic acid, 3-methyl-2-oxo-, methyl ester, commonly referred to as a methyl ester derivative of a cyclopentanecarboxylic acid, is an organic compound characterized by its cyclopentane ring structure with a carboxylic acid functional group and a methyl ester group. This compound features a ketone functionality due to the presence of the 2-oxo group, which contributes to its reactivity and potential applications in organic synthesis. Typically, it appears as a colorless to pale yellow liquid or solid, depending on the specific conditions and purity. The presence of both the ester and ketone functionalities allows for various chemical reactions, including esterification and nucleophilic additions. Its solubility in organic solvents makes it useful in various chemical processes, including as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Safety data should be consulted for handling, as with all chemical substances, to ensure proper precautions are taken due to potential irritant properties.

Formula: C₈H₁₂O₃

Methyl 3-Methyl-2-oxocyclopentane-1-carboxylate

CAS: 57964-61-1

Methyl 3-Methyl-2-oxocyclopentane-1-carboxylate

Purity: 95%

Molecular weight: 156.18g/mol

Ref: 54-OR1003142

Methyl 3-methyl-2-oxocyclopentane-1-carboxylate

CAS: 57964-61-1

Formula: C₈H₁₂O₃

Molecular weight: 156.18

Ref: 4Z-C-283071

Methyl 3-methyl-2-oxocyclopentane-1-carboxylate

CAS: 57964-61-1

Methyl 3-methyl-2-oxocyclopentane-1-carboxylate (MECCP) is a fungicide that is used in horticulture. It inhibits the growth of fungi by inhibiting the synthesis of ergosterol, which is an important component of fungal cell membranes. MECCP is synthesized by reacting cyclopentanone with acid methyl ester and sodium hydride in methanol. The product can be hydrolyzed to metconazole, which has fungicidal properties. Methyl 3-methyl-2-oxocyclopentane-1-carboxylate can also be synthesized from methyl 2-oxocyclopentane carboxylate ethyl ester and methyllithium. This compound has a high yield and can be used as a substitute for other compounds such as pentachlorophenol, which have been banned due to their toxicity to humans and animals.

Formula: C₈H₁₂O₃

Purity: Min. 95%

Molecular weight: 156.18 g/mol

Ref: 3D-HCA96461