159497-96-8

Basic information

• Product Name: tert-butyl (S)-1-<1-<2-(N,N-dibenzylamino)-4-hydroxybutyl>>-3-hydroxypyrrole-2-carboxylate
• Synonyms: tert-butyl (S)-1-<1-<2-(N,N-dibenzylamino)-4-hydroxybutyl>>-3-hydroxypyrrole-2-carboxylate
• CAS NO: 159497-96-8
• Molecular Weight: 450.578
• Mol File: 159497-96-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: tert-butyl (S)-1-<1-<2-(N,N-dibenzylamino)-4-hydroxybutyl>>-3-hydroxypyrrole-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (S)-1-<1-<2-(N,N-dibenzylamino)-4-hydroxybutyl>>-3-hydroxypyrrole-2-carboxylate(159497-96-8)
• EPA Substance Registry System: tert-butyl (S)-1-<1-<2-(N,N-dibenzylamino)-4-hydroxybutyl>>-3-hydroxypyrrole-2-carboxylate(159497-96-8)

Safety Data

• Hazardous Substances Data: 159497-96-8(Hazardous Substances Data)

Upstream product

• 159497-82-2 (S)-2-(N,N-dibenzylamino)-4-<(tert-butyldimethylsilyl)oxy>-1-butylamine 
• 159497-65-1 N,N-dibenzylasparaginic acid dibenzyl ester 
• 152299-02-0 (S)-1-<2-(N,N-dibenzylamino)-4-<(tert-butyldimethylsilyl)oxy>butyl>-N-phthalimide 
• 152298-97-0 (R)-2-<1-(N,N-dibenzylamino)-4-<(tert-butyldimethylsilyl)oxy>butyl> methanesulfonate 
• 152299-13-3 (2S)-4-{[tert-butyl(dimethyl)silyl]oxy}-2-(dibenzylamino)butan-1-ol 
• 152298-92-5 (R)-N,N-dibenzyl-4-<(tert-butyldimethylsilyl)oxy>-2-chloro-1-butylamine 
• 137428-32-1 (2S)-2-[bis(phenylmethyl)amino]-1,4-butanediol 
• 117917-40-5 2,3-Dioxo-pent-4-enoic acid tert-butyl ester 
• 137604-26-3 (S)-4-amino-3-(N,N-dibenzylamino)-1-butanol 

Downstream Products

• 159497-97-9 tert-butyl (S)-1-<1-<2-(N,N-dibenzylamino)-4-bromobutyl>>-3-hydroxypyrrole-2-carboxylate 

Relevant articles and documents

Enantiomerically pure amino alcohols and diamino alcohols from L-aspartic acid. Application to the synthesis of epi- and diepislaframine

Starting from natural aspartic acid (6) a practical method for the synthesis of enantiomerically pure 3-amino alcohols 8 including 3,4-diamino derivatives is described. After perbenzylation of 6 and reduction of both carboxylates, position 4 of the result