159000-75-6

Basic information

• Product Name: S-benzyl-D,L-penicillamine
• Synonyms: S-benzyl-D,L-penicillamine
• CAS NO: 159000-75-6
• Molecular Weight: 239.338
• Mol File: 159000-75-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: S-benzyl-D,L-penicillamine(CAS DataBase Reference)
• NIST Chemistry Reference: S-benzyl-D,L-penicillamine(159000-75-6)
• EPA Substance Registry System: S-benzyl-D,L-penicillamine(159000-75-6)

Safety Data

• Hazardous Substances Data: 159000-75-6(Hazardous Substances Data)

Upstream product

• 876511-01-2 β-benzylsulfanyl-α-hydroxy-isovaleronitrile 
• 105449-77-2 2-benzylsulfanyl-2-methylpropanal 
• 494804-47-6 β-benzylsulfanyl-α-nitro-isovaleric acid ethyl ester 
• 6642-21-3 2-acetylamino-3-methyl-crotonic acid 
• 18289-63-9 3-methyl-2-nitro-2-butenoate 
• 638-10-8 ethyl 3-methylbut-2-enoate 
• 2280-28-6 3-hydroxy-DL-valine 
• 124-41-4 sodium methylate 
• 100-53-8 phenylmethanethiol 
• 64-18-6 formic acid 
• 77920-68-4 2-acetylamino-3-methyl-crotonic acid ethyl ester 
• 52-66-4 DL-Penicillamin 
• 100-44-7 benzyl chloride 
• 5398-45-8 N-benzoyl-S-benzyl-DL-penicillamine 

Downstream Products

• 100876-47-9 S-benzyl-N-glycyl-DL-penicillamine 
• 884311-31-3 S-benzyl-N-formyl-L-penicillamine 
• 911446-29-2 S-benzyl-N-formyl-D-penicillamine 
• 86799-06-6 N-phenylacetyl-S-benzyl-D-penicillamine 
• 54536-37-7 S-benzyl-D-penicillamine 
• 54536-38-8 S-benzyl-L-penicillamine 
• 158411-82-6 (+/-)-N-formylpenicillamine 
• 158944-95-7 (+/-)-S-benzyl-N-(tert-butoxycarbonyl)penicillamine 
• 102952-10-3 S-benzyl-N-(N,N-phthaloyl-γ-glutamyl)-penicillamine 
• 80190-87-0 N-Phenylacetyl-S-benzyl-D,L-penicillamine 
• 7536-37-0 S-benzyl-N-benzyloxycarbonyl-DL-penicillamine 
• 5398-45-8 N-benzoyl-S-benzyl-DL-penicillamine 
• 34297-28-4 S-methyl-DL-penicillamine 
• 102314-08-9 S-benzyl-N-(N,N-phthaloyl-glycyl)-DL-penicillamine 

Relevant articles and documents

Preparation of Some Novel S-Nitroso Compounds as Potential Slow-release Agents of Nitric Oxide in vivo

The optimum conditions for the preparation of N-acetyl-S-nitrosopenicillamine (SNAP) 3 were determined and applied to the synthesis of the corresponding N-formyl compound 7.The nitrosation of penicillamine dipeptides was investigated and bis-thionitroso compounds 13, 18, 26 and 27 were isolated.S,S'-Dinitroso dithiol 13 showed biological activity akin to that of glyceryl trinitrate in decreasing systemic arterial blood pressure in anaesthetized rats and rabbits.Concomitant inhibition of collagen- or ADP-induced platelet aggregation was observed.