288607-57-8

Basic information

• Product Name: 2-(N-4-nitrobenzyloxycarbonylamino)-4-phosphonobutanoic acid
• Synonyms: 2-(N-4-nitrobenzyloxycarbonylamino)-4-phosphonobutanoic acid
• CAS NO: 288607-57-8
• Molecular Weight: 362.233
• Mol File: 288607-57-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(N-4-nitrobenzyloxycarbonylamino)-4-phosphonobutanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(N-4-nitrobenzyloxycarbonylamino)-4-phosphonobutanoic acid(288607-57-8)
• EPA Substance Registry System: 2-(N-4-nitrobenzyloxycarbonylamino)-4-phosphonobutanoic acid(288607-57-8)

Safety Data

• Hazardous Substances Data: 288607-57-8(Hazardous Substances Data)

Upstream product

• 6323-99-5 2-amino-4-phosphonobutyric acid 
• 4457-32-3 4-nitrobenzyl chloroformate 

Downstream Products

• 910035-14-2 ethyl 2-(N-4-nitrobenzyloxycarbonylamino)-4-[bis(4-trifluoromethylphenyl)phosphono]butanoate 
• 910035-15-3 methyl 2-(N-4-nitrobenzyloxycarbonylamino)-4-[bis(4-acetylphenyl)phosphono]butanoate 
• 910035-16-4 ethyl 2-(N-4-nitrobenzyloxycarbonylamino)-4-[bis(4-cyanophenyl)phosphono]butanoate 
• 910035-27-7 4-[hydroxy-(4-trifluoromethyl-phenoxy)-phosphoryl]-2-(4-nitro-benzyloxycarbonylamino)-butyric acid 
• 910035-29-9 4-[(4-acetyl-phenoxy)-hydroxy-phosphoryl]-2-(4-nitro-benzyloxycarbonylamino)-butyric acid 
• 910035-31-3 4-[(4-cyano-phenoxy)-hydroxy-phosphoryl]-2-(4-nitro-benzyloxycarbonylamino)-butyric acid 
• 910035-13-1 methyl 2-(N-4-nitrobenzyloxycarbonylamino)-4-(diphenylphosphono)butanoate 
• 910035-25-5 4-(hydroxy-phenoxy-phosphoryl)-2-(4-nitro-benzyloxycarbonylamino)-butyric acid 
• 910035-12-0 C₁₄H₁₇Cl₂N₂O₇P 
• 910035-11-9 C₁₃H₁₅Cl₂N₂O₇P 
• 910035-10-8 ethyl 2-(N-4-nitrobenzyloxycarbonylamino)-4-phosphonobutanoate 
• 910035-09-5 methyl 2-(N-4-nitrobenzyloxycarbonylamino)-4-phosphonobutanoate 

Relevant articles and documents

γ-(Monophenyl)phosphono glutamate analogues as mechanism-based inhibitors of γ-glutamyl transpeptidase

γ-Glutamyl transpeptidase (GGT, EC 2.3.2.2) catalyzes the hydrolysis and transpeptidation of extracellular glutathione and plays a central role in glutathione homeostasis. We report here the synthesis and evaluation of a series of hydrolytically stable γ-