312311-60-7

Basic information

• Product Name: H-β³-hPhe-N-allyl-β³-hPhe-OMe
• Synonyms: H-β³-hPhe-N-allyl-β³-hPhe-OMe
• CAS NO: 312311-60-7
• Molecular Weight: 394.514
• Mol File: 312311-60-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: H-β³-hPhe-N-allyl-β³-hPhe-OMe(CAS DataBase Reference)
• NIST Chemistry Reference: H-β³-hPhe-N-allyl-β³-hPhe-OMe(312311-60-7)
• EPA Substance Registry System: H-β³-hPhe-N-allyl-β³-hPhe-OMe(312311-60-7)

Safety Data

• Hazardous Substances Data: 312311-60-7(Hazardous Substances Data)

Upstream product

• 172695-25-9 (S)-3-<(tert-butoxycarbonyl)amino>-4-phenylbutanenitrile 
• 312311-67-4 (S)-3-(p-nitrobenzenesulfonyl)amino-4-phenylbutanoic acid 
• 312311-68-5 methyl (S)-3-(p-nitrobenzenesulfonyl)amino-4-phenylbutanoate 
• 312311-69-6 methyl (S)-3-allylamino-4-phenylbutanoate 
• 219738-95-1 (S)-N-(p-nitrobenzenesulfonyl)-2-benzylaziridine 
• 60398-42-7 methyl (3S)-3-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoate 
• 3182-95-4 L-Phenylalaninol 
• 312311-70-9 methyl N-(p-nitrobenzenesulfonyl)-(S)-β³-homophenylalanyl-N-allyl-(S)-β³-homophenylalaninate 
• 374783-82-1 (S)-3-[p-nitrobenzenesulfonyl]amino-4-phenylbutanenitrile 
• 312311-59-4 methyl (S)-3-(N-allyl-N-tert-butoxycarbonylamino)-4-phenylbutanoate 
• 312311-58-3 (S)-3-tert-butoxycarbonylamino-4-phenylbutanamide 

Downstream Products

• 223595-60-6 cyclo(N-allyl-β³-hPhe-β³-hPhe-N-allyl-β³-hPhe-β³-hPhe) 
• 312311-73-2 H-β³-hPhe-N-allyl-β³-hPhe-β³-hPhe-N-allyl-β³-hPhe-OMe 
• 312311-74-3 cyclo(N-(2-hydroxyethyl)-β³-hPhe-β³-hPhe-N-(2-hydroxyethyl)-β³-hPhe-β³-hPhe) 
• 312311-75-4 cyclo(N-(2-azidoethyl)-β³-hPhe-β³-hPhe-N-(2-azidoethyl)-β³-hPhe-β³-hPhe) 
• 312311-72-1 Ns-β³-hPhe-N-allyl-β³-hPhe-β³-hPhe-N-allyl-β³-hPhe-OMe 

Relevant articles and documents

Pseudoaxially disubstituted cyclo-β3-tetrapeptide scaffolds

An N,N-disubstituted cyclo-β3-tetrapeptide, identified as a potential molecular scaffold, has been synthesised on a multigram scale from β-homophenylalanine by employing a nosylate-based protection strategy. C2-Symmetric derivatives containing pseudoaxial, combinatorially addressable functionalities have been prepared from the parent cyclopeptide. (C) 2000 Elsevier Science Ltd.