2-Chloro-1-cyclopentylethanone, with the CAS number 932-28-5, is an organic compound characterized by its ketone functional group and a cyclopentyl substituent. It features a chloro group attached to the second carbon of the ethyl chain, which influences its reactivity and physical properties. This compound typically appears as a colorless to pale yellow liquid and has a distinctive odor. Its molecular structure contributes to its moderate polarity, affecting its solubility in various solvents; it is generally soluble in organic solvents but less so in water. The presence of the chloro group can enhance its reactivity in nucleophilic substitution reactions, making it a useful intermediate in organic synthesis. Additionally, 2-chloro-1-cyclopentylethanone may exhibit biological activity, which can be of interest in pharmaceutical research. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested. Overall, its unique structure and properties make it a valuable compound in synthetic organic chemistry.

2-Chloro-1-cyclopentylethanone

932-28-5: 2-Chloro-1-cyclopentylethanone, with the CAS number 932-28-5, is an organic compound characterized by its ketone functional group and a cyclopentyl substituent. It features a chloro group attached to the second carbon of the ethyl chain, which influences its reactivity and physical properties. This compound typically appears as a colorless to pale yellow liquid and has a distinctive odor. Its molecular structure contributes to its moderate polarity, affecting its solubility in various solvents; it is generally soluble in organic solvents but less so in water. The presence of the chloro group can enhance its reactivity in nucleophilic substitution reactions, making it a useful intermediate in organic synthesis. Additionally, 2-chloro-1-cyclopentylethanone may exhibit biological activity, which can be of interest in pharmaceutical research. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested. Overall, its unique structure and properties make it a valuable compound in synthetic organic chemistry.

<p>2-Chloro-1-cyclopentylethan-1-one is an affinity agent that binds to the gastrin receptor, which is a G protein coupled receptor. It also has high affinity for cck-a and heterocyclic group. 2-Chloro-1-cyclopentylethan-1-one is used in the treatment of peptic ulcer disease, Zollinger Ellison syndrome, and dyspepsia. It is also used as an anxiolytic and a sedative drug. 2CPCEO has been shown to be a benzodiazepine with a hydrogen atom. This benzodiazepine has an alkoxycarbonyl group at the end of its structure.</p>

CAS 932-28-5

2-Chloro-1-cyclopentylethanone

2-Chloro-1-cyclopentylethan-1-one

Ref: 3D-AAA93228