179083-46-6

Basic information

• Product Name: (S)-4-tert-Butoxycarbonylamino-4-phenylcarbamoyl-butyric acid tert-butyl ester
• CAS NO: 179083-46-6
• Molecular Weight: 378.469
• Mol File: 179083-46-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-4-tert-Butoxycarbonylamino-4-phenylcarbamoyl-butyric acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-tert-Butoxycarbonylamino-4-phenylcarbamoyl-butyric acid tert-butyl ester(179083-46-6)
• EPA Substance Registry System: (S)-4-tert-Butoxycarbonylamino-4-phenylcarbamoyl-butyric acid tert-butyl ester(179083-46-6)

Safety Data

• Hazardous Substances Data: 179083-46-6(Hazardous Substances Data)

Upstream product

• 13726-84-6 Boc-Glu(OtBu)-OH 
• 62-53-3 aniline 

Downstream Products

• 179083-47-7 (S)-4-tert-Butoxycarbonylamino-4-({[isopropyl-(4-methoxy-phenyl)-carbamoyl]-methyl}-phenyl-carbamoyl)-butyric acid tert-butyl ester 

Relevant articles and documents

Conversion of acyclic nonpeptide CCK antagonists into CCK agonists

The CCK antagonists RP 69758 and (R)-lorglumide were converted into CCK agonists by the introduction of an N-isopropylanilide agonist 'trigger'. The common structural features of these ligands suggest that nonpeptide agonists and antagonists bind to a common site in the CCK receptor.