Methyl (S)-2-cyclopentyl-2-hydroxy-2-phenylacetate, identified by its CAS number 860644-54-8, is an organic compound characterized by its ester functional group, which is derived from the reaction of a carboxylic acid and an alcohol. This compound features a chiral center, indicated by the (S) configuration, which contributes to its potential biological activity and specificity in interactions. The presence of the cyclopentyl and phenyl groups enhances its structural complexity and may influence its solubility and reactivity. Typically, esters like this one exhibit pleasant, fruity odors and are often used in flavoring and fragrance applications. Additionally, the hydroxyl group (–OH) introduces polarity, which can affect the compound's solubility in various solvents. The compound's stereochemistry and functional groups suggest potential applications in pharmaceuticals or as intermediates in organic synthesis, where chirality can play a crucial role in the efficacy of the resulting products. Overall, its unique structure and properties make it a compound of interest in both synthetic and applied chemistry contexts.

methyl (S)-2-cyclopentyl-2-hydroxy-2-phenylacetate

860644-54-8: Methyl (S)-2-cyclopentyl-2-hydroxy-2-phenylacetate, identified by its CAS number 860644-54-8, is an organic compound characterized by its ester functional group, which is derived from the reaction of a carboxylic acid and an alcohol. This compound features a chiral center, indicated by the (S) configuration, which contributes to its potential biological activity and specificity in interactions. The presence of the cyclopentyl and phenyl groups enhances its structural complexity and may influence its solubility and reactivity. Typically, esters like this one exhibit pleasant, fruity odors and are often used in flavoring and fragrance applications. Additionally, the hydroxyl group (–OH) introduces polarity, which can affect the compound's solubility in various solvents. The compound's stereochemistry and functional groups suggest potential applications in pharmaceuticals or as intermediates in organic synthesis, where chirality can play a crucial role in the efficacy of the resulting products. Overall, its unique structure and properties make it a compound of interest in both synthetic and applied chemistry contexts.

CAS 860644-54-8

methyl (S)-2-cyclopentyl-2-hydroxy-2-phenylacetate

Glycopyrrolate Impurity 22

Ref: 4Z-G-3238

Glycopyrrolate Impurity 22

Ref: ST-EA-CP-G2030