Methyl (1R,3S)-3-hydroxycyclopentanecarboxylate is an organic compound characterized by its cyclopentane ring structure, which features a hydroxyl group (-OH) and a carboxylate ester functional group. The compound is chiral, with specific stereochemistry indicated by the (1R,3S) configuration, which affects its physical and chemical properties, including its reactivity and interactions with biological systems. It is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. The presence of the hydroxyl group contributes to its potential solubility in polar solvents, while the ester functionality may influence its reactivity in esterification and hydrolysis reactions. This compound may be of interest in synthetic organic chemistry, particularly in the development of pharmaceuticals or agrochemicals, due to its structural features that can serve as a scaffold for further chemical modifications. Additionally, its specific stereochemistry may impart unique biological activities, making it a candidate for further research in medicinal chemistry.

methyl (1R,3S)-3-hydroxycyclopentanecarboxylate

79598-73-5: Methyl (1R,3S)-3-hydroxycyclopentanecarboxylate is an organic compound characterized by its cyclopentane ring structure, which features a hydroxyl group (-OH) and a carboxylate ester functional group. The compound is chiral, with specific stereochemistry indicated by the (1R,3S) configuration, which affects its physical and chemical properties, including its reactivity and interactions with biological systems. It is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. The presence of the hydroxyl group contributes to its potential solubility in polar solvents, while the ester functionality may influence its reactivity in esterification and hydrolysis reactions. This compound may be of interest in synthetic organic chemistry, particularly in the development of pharmaceuticals or agrochemicals, due to its structural features that can serve as a scaffold for further chemical modifications. Additionally, its specific stereochemistry may impart unique biological activities, making it a candidate for further research in medicinal chemistry.

CAS 79598-73-5

methyl (1R,3S)-3-hydroxycyclopentanecarboxylate

(cis)-3-Hydroxy-cyclopentanecarboxylic ac id Methyl ester

Ref: IN-DA00G9X3

Methyl cis-3-hydroxycyclopentane-1-carboxylate

Ref: 54-OR52665

methyl cis-3-hydroxycyclopentane-1-carboxylate

Ref: 10-F519319