223595-66-2

Basic information

• Product Name: methyl N-tert-butoxycarbonyl-(S)-β³-homophenylalanyl-N-allyl-(S)-β³-homophenylalaninate
• Synonyms: methyl N-tert-butoxycarbonyl-(S)-β³-homophenylalanyl-N-allyl-(S)-β³-homophenylalaninate
• CAS NO: 223595-66-2
• Molecular Weight: 494.631
• Mol File: 223595-66-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl N-tert-butoxycarbonyl-(S)-β³-homophenylalanyl-N-allyl-(S)-β³-homophenylalaninate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl N-tert-butoxycarbonyl-(S)-β³-homophenylalanyl-N-allyl-(S)-β³-homophenylalaninate(223595-66-2)
• EPA Substance Registry System: methyl N-tert-butoxycarbonyl-(S)-β³-homophenylalanyl-N-allyl-(S)-β³-homophenylalaninate(223595-66-2)

Safety Data

• Hazardous Substances Data: 223595-66-2(Hazardous Substances Data)

Upstream product

• 51871-62-6 (S)-3-tert-butoxycarbonylamino-4-phenylbutanoic acid 
• 60398-42-7 methyl (3S)-3-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoate 
• 172695-25-9 (S)-3-<(tert-butoxycarbonyl)amino>-4-phenylbutanenitrile 
• 312311-58-3 (S)-3-tert-butoxycarbonylamino-4-phenylbutanamide 
• 24424-99-5 di-tert-butyl dicarbonate 
• 3182-95-4 L-Phenylalaninol 
• 66605-57-0 (S)-N-tert-butoxycarbonyl-2-amino-3-phenylpropanol 

Downstream Products

• 312311-75-4 cyclo(N-(2-azidoethyl)-β³-hPhe-β³-hPhe-N-(2-azidoethyl)-β³-hPhe-β³-hPhe) 
• 312311-74-3 cyclo(N-(2-hydroxyethyl)-β³-hPhe-β³-hPhe-N-(2-hydroxyethyl)-β³-hPhe-β³-hPhe) 
• 312311-63-0 Boc-β³-hPhe-N-allyl-β³-hPhe-β³-hPhe-N-allyl-β³-hPhe-OC6F5 
• 223595-70-8 H-β³-hPhe-N-allyl-β³-hPhe-β³-hPhe-N-allyl-β³-hPhe-OC6F5 
• 312311-62-9 Boc-β³-hPhe-N-allyl-β³-hPhe-β³-hPhe-N-allyl-β³-hPhe-OH 
• 223595-69-5 Boc-β³-hPhe-N-allyl-β³-hPhe-β³-hPhe-N-allyl-β³-hPhe-OMe 
• 223595-60-6 cyclo(N-allyl-β³-hPhe-β³-hPhe-N-allyl-β³-hPhe-β³-hPhe) 
• 223595-67-3 Boc-β³-hPhe-N-allyl-β³-hPhe-OH 

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.