312921-96-3

Basic information

• Product Name: Benzoic acid, 3-nitro-4-[[3-(2-oxo-1-pyrrolidinyl)propyl]amino]-
• CAS NO: 312921-96-3
• Molecular Formula: C14H17N3O5
• Molecular Weight: 307.306
• Mol File: 312921-96-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 3-nitro-4-[[3-(2-oxo-1-pyrrolidinyl)propyl]amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 3-nitro-4-[[3-(2-oxo-1-pyrrolidinyl)propyl]amino]-(312921-96-3)
• EPA Substance Registry System: Benzoic acid, 3-nitro-4-[[3-(2-oxo-1-pyrrolidinyl)propyl]amino]-(312921-96-3)

Safety Data

• Hazardous Substances Data: 312921-96-3(Hazardous Substances Data)

Upstream product

• 3001-72-7 DBN 
• 7663-77-6 1-(3-aminopropyl)-2-pyrrolidone 
• 96-99-1 4-chloro-3-nitrobenzoate 

Downstream Products

• 1270171-51-1 N,N-dimethylaminopropyl-4-[N-(3'-aminopropyl)-2-pyrrolidone]-3-nitrobenzoate 
• 1270171-55-5 N,N-diethylaminopropyl-4-[N-(3'-aminopropyl)-2-pyrrolidone]-3-nitrobenzoate 

Relevant articles and documents

Synthesis of potentially bioactive PABA-related N-(aminoalkyl)lactamic amino acids and esters via selective SNAr reactions

Potentially bioactive N-(aminoalkyl)lactamic amino acids and esters were synthesized in satisfactory to good yields by SNAr reactions of aromatic acids with N-(3-aminopropyl)lactams followed by esterification with tertiary amino alcohols. The addition-elimination SNAr mechanism was confirmed by NMR and MS measurements. Graphical Abstract: [Figure not available: see fulltext.]