62982-13-2

Basic information

• Product Name: L-Cysteine, N-[(1,1-dimethylethoxy)carbonyl]-S-(diphenyl-4-pyridinylmethyl)-
• CAS NO: 62982-13-2
• Molecular Formula: C26H28N2O4S
• Molecular Weight: 464.585
• Mol File: 62982-13-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: L-Cysteine, N-[(1,1-dimethylethoxy)carbonyl]-S-(diphenyl-4-pyridinylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: L-Cysteine, N-[(1,1-dimethylethoxy)carbonyl]-S-(diphenyl-4-pyridinylmethyl)-(62982-13-2)
• EPA Substance Registry System: L-Cysteine, N-[(1,1-dimethylethoxy)carbonyl]-S-(diphenyl-4-pyridinylmethyl)-(62982-13-2)

Safety Data

• Hazardous Substances Data: 62982-13-2(Hazardous Substances Data)

Upstream product

• 62982-14-3 N-t-butoxycarbonyl-S-(diphenyl-4-pyridylmethyl)-L-cysteine dicyclohexylammonium salt 
• 14548-46-0 4-Benzoylpyridine 
• 1070-19-5 N-(tert-butyloxycarbonyl) azide 
• 62982-12-1 S-(diphenyl-4-pyridylmethyl)-L-cysteine 
• 1620-30-0 diphenyl(pyridin-4-yl)methanol 

Downstream Products

• 62982-19-8 Boc-Ile-Ala-Cys(Dppm)-Ala-Cys(Dppm)-Ala-OPic 
• 64991-58-8 N-t-butoxycarbonyl-S-(diphenyl-4-pyridylmethyl)-L-cysteinyl-L-alanine 
• 62982-18-7 S-(diphenyl-4-pyridylmethyl)-L-cysteinyl-L-alanine 
• 64991-57-7 Boc-Cys(Dppm)-Ala-OPic 
• 64991-54-4 N-t-butoxycarbonyl-S-(diphenyl-4-pyridylmethyl)-L-cysteine pentachlorophenyl ester 
• 64991-53-3 N-t-butoxycarbonyl-S-(diphenyl-4-pyridylmethyl)-L-cysteine ethyl ester 
• 10389-65-8 di-t-butoxycarbonyl-L-cystine 
• 64991-52-2 N-t-butoxycarbonyl-S-(diphenyl-4-pyridylmethyl)-L-cysteine methyl ester 

Relevant articles and documents

Amino-acids and Peptides. Part 45. The Protection of the Thiol Function of Cysteine and the Imidazole-N of Histidine by the Diphenyl-4-pyridylmethyl Group

S-(Diphenyl-4-pyridylmethyl)-L-cysteine (1) and its derivatives (2)-(7) have been prepared and used in peptide synthesis.In contrast to the analogous S-trityl group, this protection is stable in acid but it is cleaved readily by zinc-acetic acid, by mercury(II) acetate, by iodine, and by electrolytic reduction.N(Im)-Diphenyl-4-pyridylmethyl-L-histidine derivatives (9)-(13) are also reported; the protecting group is again stable to acid but cleaved by hydrogenolysis, by zinc-acetic acid, and by electrolytic reduction, and it has been used in the synthesis of L-histidyl-L-leucine, -L-phenylalanine, and -glycine.