192064-99-6

Basic information

• Product Name: (S)-2-((S)-2-tert-Butoxycarbonylamino-3,3-diphenyl-propionylamino)-3-(1H-imidazol-4-yl)-propionic acid methyl ester
• Synonyms: (S)-2-((S)-2-tert-Butoxycarbonylamino-3,3-diphenyl-propionylamino)-3-(1H-imidazol-4-yl)-propionic acid methyl ester
• CAS NO: 192064-99-6
• Molecular Weight: 492.575
• Mol File: 192064-99-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-((S)-2-tert-Butoxycarbonylamino-3,3-diphenyl-propionylamino)-3-(1H-imidazol-4-yl)-propionic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-((S)-2-tert-Butoxycarbonylamino-3,3-diphenyl-propionylamino)-3-(1H-imidazol-4-yl)-propionic acid methyl ester(192064-99-6)
• EPA Substance Registry System: (S)-2-((S)-2-tert-Butoxycarbonylamino-3,3-diphenyl-propionylamino)-3-(1H-imidazol-4-yl)-propionic acid methyl ester(192064-99-6)

Safety Data

• Hazardous Substances Data: 192064-99-6(Hazardous Substances Data)

Upstream product

• 138662-63-2 (2S)-2-tert-butoxycarbonylamino-3,3-diphenyl-propionic acid 
• 4467-54-3 l-histidine methyl ester dihydrochloride 

Relevant articles and documents

Studies on Cyclic Dipeptides, II [1a]. Methylated Modifications of cyclo-[Phe-His]

Synthesis of seven new cyclic dipeptides and their conformational analysis based on 1HNMR spectra is reported as well as their application as models to elucidate the mechanism of cyclic dipeptide catalysis in enantioselective mandelonitrile formation. Further evidence is presented to support the view that a highly ordered supramolecular complex of dipeptides acts as catalyst.