153152-98-8

Basic information

• Product Name: (1R,2S,1'R,2'S)-2-(2'-tert-butoxycarbonylamino-1'-hydroxy-3'-phenylpropyl)cyclopentane-1-carboxylic acid n-butylamide
• Synonyms: (1R,2S,1'R,2'S)-2-(2'-tert-butoxycarbonylamino-1'-hydroxy-3'-phenylpropyl)cyclopentane-1-carboxylic acid n-butylamide
• CAS NO: 153152-98-8
• Molecular Weight: 418.577
• Mol File: 153152-98-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1R,2S,1'R,2'S)-2-(2'-tert-butoxycarbonylamino-1'-hydroxy-3'-phenylpropyl)cyclopentane-1-carboxylic acid n-butylamide(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S,1'R,2'S)-2-(2'-tert-butoxycarbonylamino-1'-hydroxy-3'-phenylpropyl)cyclopentane-1-carboxylic acid n-butylamide(153152-98-8)
• EPA Substance Registry System: (1R,2S,1'R,2'S)-2-(2'-tert-butoxycarbonylamino-1'-hydroxy-3'-phenylpropyl)cyclopentane-1-carboxylic acid n-butylamide(153152-98-8)

Safety Data

• Hazardous Substances Data: 153152-98-8(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 153077-97-5 (1R,2S,1'S,2'S)-2-(2'-tert-butoxycarbonylamino-1'-hydroxy-3'-phenylpropyl)cyclopentane-1-carboxylic acid n-butylamide 
• 130372-24-6 (1R,1'S,2S,2'S)-2-<2'-<(Boc)amino>-1'-hydroxy-3'-phenylpropyl>cyclopentanecarboxylic acid lactone 
• 109-73-9 N-butylamine 
• 153152-96-6 (1R,4R,5S,1'S)-4-(1'-N-tert-butoxycarbonylamino-2'-phenyl)ethyl-3-oxobicyclo<3.3.0>octan-2-one 

Downstream Products

• 155320-54-0 (4S,5R,1'S,2'S)-4-benzyl-3-N-tert-butoxycarbonyl-5-(2'-n-butylaminocarbonyl)cyclopentyl-2,2-dimethyloxazolidine 
• 153152-96-6 (1R,4R,5S,1'S)-4-(1'-N-tert-butoxycarbonylamino-2'-phenyl)ethyl-3-oxobicyclo<3.3.0>octan-2-one 
• 155320-50-6 (4S,5R,1'S,2'R)-4-benzyl-3-N-tert-butoxycarbonyl-5-(2'-n-butylaminocarbonyl)cyclopentyl-2,2-dimethyloxazolidine 

Relevant articles and documents

A new synthetic route for the γ-lactone precursors of hydroxyethylene dipeptide isosteres

δ-Phthalimido-γ-ketoesters were obtained by the Pd catalyzed coupling reaction between acid chlorides and organozinc reagents derived from β-iodoesters, and were converted into the γ-lactones precursors of Phe-ψ[H.E.]-Ala and Phe-ψ[H.E.]-Pro (15a,b-18a,b).