88050-23-1

Basic information

• Product Name: L-Glutamic acid, N-(4-nitrobenzoyl)-, bis(1,1-dimethylethyl) ester
• CAS NO: 88050-23-1
• Molecular Formula: C20H28N2O7
• Molecular Weight: 408.452
• Mol File: 88050-23-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: L-Glutamic acid, N-(4-nitrobenzoyl)-, bis(1,1-dimethylethyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Glutamic acid, N-(4-nitrobenzoyl)-, bis(1,1-dimethylethyl) ester(88050-23-1)
• EPA Substance Registry System: L-Glutamic acid, N-(4-nitrobenzoyl)-, bis(1,1-dimethylethyl) ester(88050-23-1)

Safety Data

• Hazardous Substances Data: 88050-23-1(Hazardous Substances Data)

Upstream product

• 16874-06-9 Glutamic acid di-tert-butyl ester 
• 122-04-3 4-nitro-benzoyl chloride 
• 16874-06-9 di-tert-butyl L-glutamate 
• 62-23-7 4-nitro-benzoic acid 
• 32677-01-3 L-glutamic acid di-tert-butyl ester hydrochloride 

Downstream Products

• 123724-56-1 di-tert-butyl 4-<(2-chloroethyl)<2-(mesyloxy)ethyl>amino>benzoyl-L-glutamate 
• 122665-73-0 CMDA 
• 123724-56-1 Di-tert-butyl 4-<(2-chloroethyl)(2-mesyloxyethyl)amino>benzoyl-L-glutamate 
• 122665-73-0 4-<(2-Chloroethyl)(2-mesyloxyethyl)amino>benzoyl-L-glutamic acid 
• 130633-37-3 Di-tert-butyl 4-<(2-chloroethyl)(2-hydroxyethyl)amino>benzoyl-L-glutamate 
• 130633-36-2 Di-tert-butyl 4-<(2-chloroethyl)amino>benzoyl-L-glutamate 
• 93502-97-7 (S)-2-{4-[(2,4-Diamino-quinazolin-6-ylmethyl)-amino]-benzoylamino}-pentanedioic acid di-tert-butyl ester 
• 61075-41-0 10-formyl-5,8-dideazaaminopterin 
• 27244-49-1 5,8-dideazamethopterin 
• 18921-68-1 5,8-dideazaaminopterin 
• 76282-66-1 Di-tert-butyl 4-aminobenzoyl-L-glutamate 

Relevant articles and documents

Dienophilicity of imidazole in inverse electron demand Diels-Alder reactions. 4. Intermolecular reactions with 1,2,4-triazines

Intermolecular inverse electron demand cycloadditions of 2-substituted imidazoles with various 1,2,4-triazines produced both imidazo[4,5-c]pyridines (3-deazapurines) and pyrido[3,2-d]pyrimid-4-ones (8-deazapteridines). The product distribution was control

Novel Prodrugs Which Are Activated to Cytotoxic Alkylating Agents by Carboxypeptidase G2

The synthesis of three novel prodrugs, 4-amino>benzoyl-L-glutamic acid (7), 4-amino>benzoyl-L-glutamic acid (8), and 4-benzoyl-L-glutamic acid (9), for use as anticancer ag