716345-81-2

Basic information

• Product Name: [2-hydroxy-1-(2-nitro-phenyl)-ethyl]-carbamic acid tert-butyl ester
• Synonyms: [2-hydroxy-1-(2-nitro-phenyl)-ethyl]-carbamic acid tert-butyl ester
• CAS NO: 716345-81-2
• Molecular Weight: 282.296
• Mol File: 716345-81-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [2-hydroxy-1-(2-nitro-phenyl)-ethyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [2-hydroxy-1-(2-nitro-phenyl)-ethyl]-carbamic acid tert-butyl ester(716345-81-2)
• EPA Substance Registry System: [2-hydroxy-1-(2-nitro-phenyl)-ethyl]-carbamic acid tert-butyl ester(716345-81-2)

Safety Data

• Hazardous Substances Data: 716345-81-2(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 716345-79-8 2-amino-2-(o-nitrophenyl)ethanol 
• 239077-32-8 methyl t-butoxycarbonyloxy-2'-nitrophenylglycinate 
• 716345-77-6 2-azido-2-(o-nitrophenyl)ethanol 
• 51673-59-7 1-(2-nitrophenyl)ethane-1,2-diol 

Downstream Products

• 716346-07-5 C₆₀H₉₄N₂₀O₁₁S 
• 606976-06-1 1-(2-nitrophenyl)-2-(triphenylmethylthio)ethylamine 
• 716345-85-6 thioacetic acid S-[2-tert-butoxycarbonylamino-2-(2-nitro-phenyl)-ethyl] ester 
• 716345-87-8 [2-mercapto-1-(2-nitro-phenyl)-ethyl]-carbamic acid tert-butyl ester 
• 716345-83-4 toluene-4-sulfonic acid 2-tert-butoxycarbonylamino-2-(2-nitro-phenyl)-ethyl ester 
• 239077-33-9 [1-(2-amino-phenyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester 

Relevant articles and documents

An o-nitrobenzyl scaffold for peptide ligation: Synthesis and applications

Chemical ligation approaches facilitate the chemoselective assembly of unprotected peptides in aqueous solution. Here, two photolabile auxiliaries are described that enlarge the applicability of native chemical ligation to non-cysteine targets. The auxili

Synthesis and protein kinase C binding activity of benzolactam-V7

Benzolactam-V7 (3a), a simplified analogues of (-)-indolactam-V with twist-form conformation, was synthesized and evaluated as a new protein kinase C modulator. Both 3a and its-7-substituted analogue 3c showed weak binding activity to displace PDBU binding from recombinant PKCα.