161531-12-0

Basic information

• Product Name: (S)-1-(3-N,N-dibenzylamino-4-hydroxy)butylmethanesulfonate
• Synonyms: (S)-1-(3-N,N-dibenzylamino-4-hydroxy)butylmethanesulfonate
• CAS NO: 161531-12-0
• Molecular Weight: 363.478
• Mol File: 161531-12-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-1-(3-N,N-dibenzylamino-4-hydroxy)butylmethanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-(3-N,N-dibenzylamino-4-hydroxy)butylmethanesulfonate(161531-12-0)
• EPA Substance Registry System: (S)-1-(3-N,N-dibenzylamino-4-hydroxy)butylmethanesulfonate(161531-12-0)

Safety Data

• Hazardous Substances Data: 161531-12-0(Hazardous Substances Data)

Upstream product

• 124-63-0 methanesulfonyl chloride 
• 137428-32-1 (2S)-2-[bis(phenylmethyl)amino]-1,4-butanediol 
• 159497-65-1 N,N-dibenzylasparaginic acid dibenzyl ester 

Downstream Products

• 152298-86-7 (S)-1-(3-N,N-dibenzylamino-4-tert-butyldimethylsilyloxy)butylmethanesulfonate 
• 128916-03-0 (S)-2-N,N-dibenzylamino-4-(1-pyrrolyl)-1-butanol 
• 152298-88-9 (2S)-N,N-dibenzyl-2-aminopentan-1-ol 
• 152298-87-8 (S)-N,N-dibenzyl-2-(1-tert-butyldimethylsilyloxy)pentylamine 
• 152298-89-0 (S)-2-N,N-dibenzylamino-4-(1-pyrazolyl)butanal 
• 152299-08-6 (S)-2-N,N-dibenzylamino-4-(1-pyrazolyl)-1-butanol 
• 152298-98-1 (S)-N,N-dibenzyl-2-(1-tert-butyldimethylsilyloxy-4-phenyl)butylamine 
• 152299-00-8 (S)-N,N-dibenzyl-2-<1-tert-butyldimethylsilyloxy-4-(1-pyrazolyl)>butylamine 
• 152299-07-5 (S)-1-(3-N,N-dibenzylamino-4-hydroxy)butyl-N-phthalimide 
• 152298-99-2 (S)-1-(3-N,N-dibenzylamino-5-tert-butyldimethylsilyloxy)butyl-N-phthalimide 
• 161531-08-4 (S)-4-N,N-dibenzylamino-5-tert-butyldimethylsilyloxy-1-pentanenitrile 
• 161531-10-8 (S)-N,N-dibenzyl-2-<1-tert-butyldimethylsilyloxy-4-(1-pyrrolyl)>butylamine 
• 161531-07-3 (S)-2-N,N-dibenzylamino-4-(1-indolyl)-1-butanol 
• 161531-09-5 (S)-N,N-dibenzyl-2-(4-azido-1-tert-butyldimethylsilyloxy)butylamine 

Relevant articles and documents

2-Dibenzylaminobutane-1,4-diol: An Effective Chiral Building Block for the Synthesis of 1,2-Amino Alcohols

Regioselective activation and protection of the chiral building block 1, readly available from L-aspartic acid, leads to the key intermediate 8.Employing classical nucleophiles, heterocyclic anions or organocuprates, 8 could be transformed into the displa