CAS 30680-84-3
:Cyclopentanecarboxylic acid, 1-methyl-2-oxo-, methyl ester
Description:
Cyclopentanecarboxylic acid, 1-methyl-2-oxo-, methyl ester, identified by CAS number 30680-84-3, is an organic compound characterized by its cyclopentane ring structure with a carboxylic acid functional group and a methyl ester moiety. This compound typically exhibits a moderate polarity due to the presence of the ester and carboxylic acid groups, which can engage in hydrogen bonding. It is likely to be a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. The compound may have a pleasant odor, common to many esters. Its solubility in organic solvents is generally good, while its solubility in water may be limited due to the hydrophobic cyclopentane ring. Cyclopentanecarboxylic acid derivatives are often studied for their potential applications in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper precautions are taken.
Formula:C8H12O3
InChI:InChI=1S/C8H12O3/c1-8(7(10)11-2)5-3-4-6(8)9/h3-5H2,1-2H3
InChI key:InChIKey=TZHZMYGNHVTEFA-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1(C)C(=O)CCC1
Synonyms:- 2-Methyl-2-carbomethoxycyclopentanone
- Cyclopentanecarboxylic acid, 1-methyl-2-oxo-, methyl ester
- Methyl 1-methyl-2-oxo-1-cyclopentanecarboxylate
- Methyl 1-methyl-2-oxocyclopentanecarboxylate
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Found 5 products.
Methyl 1-methyl-2-oxocyclopentanecarboxylate
CAS:Methyl 1-methyl-2-oxocyclopentanecarboxylatePurity:95%Molecular weight:156.18g/molmethyl 1-methyl-2-oxocyclopentane-1-carboxylate
CAS:Formula:C8H12O3Purity:95.0%Molecular weight:156.181Methyl 1-methyl-2-oxocyclopentane-1-carboxylate
CAS:<p>Methyl 1-methyl-2-oxocyclopentane-1-carboxylate is an enantiomer of methyl 1-methylcyclohexane carboxylate. This compound is prepared by reduction of the corresponding aldehyde with lithium aluminum hydride, followed by cyclization with hydrochloric acid. The product is then converted to the corresponding alcohol by reaction with dimethylformamide and sodium methoxide. Methyl 1-methyl-2-oxocyclopentane-1-carboxylate has been used in the synthesis of a number of chiral secondary alcohols. The resulting diastereomers are separated using column chromatography or recrystallization to provide pure enantiomers. Voltammetry may also be used to determine the chiral purity of these compounds.</p>Formula:C8H12O3Purity:Min. 95%Molecular weight:156.18 g/mol




