944280-95-9

Basic information

• Product Name: 1-[[(4-benzoyl-1-piperazinyl)carbonyl]amino]cyclohexanecarboxylic acid phenylmethyl ester
• Synonyms: 1-[[(4-benzoyl-1-piperazinyl)carbonyl]amino]cyclohexanecarboxylic acid phenylmethyl ester
• CAS NO: 944280-95-9
• Molecular Weight: 449.55
• Mol File: 944280-95-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-[[(4-benzoyl-1-piperazinyl)carbonyl]amino]cyclohexanecarboxylic acid phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[[(4-benzoyl-1-piperazinyl)carbonyl]amino]cyclohexanecarboxylic acid phenylmethyl ester(944280-95-9)
• EPA Substance Registry System: 1-[[(4-benzoyl-1-piperazinyl)carbonyl]amino]cyclohexanecarboxylic acid phenylmethyl ester(944280-95-9)

Safety Data

• Hazardous Substances Data: 944280-95-9(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 102373-23-9 1-aminocyclohexanecarboxylic acid benzyl ester 
• 13754-38-6 N-Benzoylpiperazine 

Relevant articles and documents

Cycloalkylcarbonylamino Acid Derivative and Process For Producing The Same

Cycloalkylcarbonylamino acid derivatives, which are raw material intermediates of a novel cycloalkane carboxamide derivative that selectively inhibits cathepsin K, and a production process thereof, are provided. A cycloalkylcarbonylamino acid derivative r

OXAZOLONE DERIVATIVE

Novel raw material compounds are provided that are useful for producing novel cycloalkane carboxamide derivatives having cathepsin K inhibitory action. An oxazolone derivative represented by formula (I): [wherein, R1 represents a substituted or unsubstituted alkyl group, substituted or unsubstituted alkenyl group, substituted or unsubstituted alkynyl group, substituted phenyl group, substituted or unsubstituted naphthyl group or substituted or unsubstituted heterocyclic group, and ring A represents a saturated cyclic alkylidene group having 6 to 7 carbon atoms].