173601-19-9

Basic information

• Product Name: 3-((S)-1-tert-Butoxycarbonylamino-4-hydroxy-butyl)-benzoic acid butyl ester
• Synonyms: 3-((S)-1-tert-Butoxycarbonylamino-4-hydroxy-butyl)-benzoic acid butyl ester
• CAS NO: 173601-19-9
• Molecular Weight: 365.47
• Mol File: 173601-19-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-((S)-1-tert-Butoxycarbonylamino-4-hydroxy-butyl)-benzoic acid butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-((S)-1-tert-Butoxycarbonylamino-4-hydroxy-butyl)-benzoic acid butyl ester(173601-19-9)
• EPA Substance Registry System: 3-((S)-1-tert-Butoxycarbonylamino-4-hydroxy-butyl)-benzoic acid butyl ester(173601-19-9)

Safety Data

• Hazardous Substances Data: 173601-19-9(Hazardous Substances Data)

Upstream product

• 201230-82-2 carbon monoxide 
• 173601-18-8 [(S)-1-(3-Bromo-phenyl)-4-hydroxy-butyl]-carbamic acid tert-butyl ester 
• 71-36-3 butan-1-ol 
• 173601-16-6 (S)-4-(3-Bromo-phenyl)-4-((S)-2-hydroxy-1-phenyl-ethylamino)-butan-1-ol 
• 173601-15-5 (S)-2-[(S)-1-(3-Bromo-phenyl)-but-3-enylamino]-2-phenyl-ethanol 
• 173601-17-7 (S)-4-Amino-4-(3-bromo-phenyl)-butan-1-ol 
• 3132-99-8 m-bromobenzoic aldehyde 

Downstream Products

• 173601-21-3 C₃₇H₄₆N₄O₈ 

Relevant articles and documents

Asymmetric Synthesis of a Novel Phenylogous Amino Acid Mimicking an Extended Dipeptide

Synthesis of an orthogonally protected form of phenylogous amino acid 1 which mimics an extended conformation of the dipeptide Arg-Gly was achieved.Key steps involve a diastereoselective addition of allylic organometallic reagents to chiral imine 2 and a palladium mediated carboalkoxylation of aryl bromide 5.