501097-16-1

Basic information

• Product Name: Glycine, N-[3-[[(4-methoxyphenyl)diphenylmethyl]amino]propyl]-N-[(2-nitrophenyl) sulfonyl]-, 1,1-dimethylethyl ester
• CAS NO: 501097-16-1
• Molecular Formula: C35H39N3O7S
• Molecular Weight: 645.777
• Mol File: 501097-16-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Glycine, N-[3-[[(4-methoxyphenyl)diphenylmethyl]amino]propyl]-N-[(2-nitrophenyl) sulfonyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-[3-[[(4-methoxyphenyl)diphenylmethyl]amino]propyl]-N-[(2-nitrophenyl) sulfonyl]-, 1,1-dimethylethyl ester(501097-16-1)
• EPA Substance Registry System: Glycine, N-[3-[[(4-methoxyphenyl)diphenylmethyl]amino]propyl]-N-[(2-nitrophenyl) sulfonyl]-, 1,1-dimethylethyl ester(501097-16-1)

Safety Data

• Hazardous Substances Data: 501097-16-1(Hazardous Substances Data)

Upstream product

• 14470-28-1 mono-4-methoxytrityl chloride 
• 1694-92-4 2-Nitrobenzenesulfonyl chloride 
• 501097-15-0 N-(4-monomethoxytrityl)-3-bromopropylamine 
• 552847-32-2 tert-butyl 2-[(2-nitrobenzene)sulfonamido]acetate 

Downstream Products

• 501097-20-7 [{3-[(3-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-propyl)-(2-nitro-benzenesulfonyl)-amino]-propyl}-(2-nitro-benzenesulfonyl)-amino]-acetic acid tert-butyl ester 
• 501097-26-3 [tert-butoxycarbonyl-(3-{[(4-methoxy-phenyl)-diphenyl-methyl]-amino}-propyl)-amino]-acetic acid tert-butyl ester 
• 501097-19-4 {(2-nitro-benzenesulfonyl)-[3-(2-nitro-benzenesulfonylamino)-propyl]-amino}-acetic acid tert-butyl ester 

Relevant articles and documents

Modelling, synthesis and biological evaluation of an ethidium-arginine conjugate linked to a ribonuclease mimic directed against TAR RNA of HIV-1

Using molecular modelling studies, an active anti-HIV ethidium-arginine conjugate targeted against the viral TAR RNA sequence has been linked to an artificial ribonuclease, with the aim to obtain an irreversible inhibitor. The ribonuclease moiety consists of an N-[N-(3-aminopropyl)-3-aminopropyl] glycine and has been constructed via two successive N-alkylations following the Fukuyama procedure.