70079-91-3

Basic information

• Product Name: Benzene, 1-(2-azidoethyl)-4-nitro-
• CAS NO: 70079-91-3
• Molecular Formula: C8H8N4O2
• Molecular Weight: 192.177
• Mol File: 70079-91-3.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(2-azidoethyl)-4-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(2-azidoethyl)-4-nitro-(70079-91-3)
• EPA Substance Registry System: Benzene, 1-(2-azidoethyl)-4-nitro-(70079-91-3)

Safety Data

• Hazardous Substances Data: 70079-91-3(Hazardous Substances Data)

Upstream product

• 20020-28-4 <(p-Nitrophenyl)ethyl>-β-sulfonic ester 
• 5339-26-4 (4-nitrophenyl)ethyl bromide 
• 100-27-6 2-(4-nitrophenyl)ethanol 

Downstream Products

• 24954-67-4 2-(p-nitrophenyl)ethylamine 
• 29968-78-3 2-(4-nitrophenyl)ethylamine monohydrochloride 
• 1602733-20-9 C₂₃H₂₀N₆O₃ 
• 1602731-97-4 C₂₃H₂₀N₆O₃ 
• 1316652-17-1 C₁₇H₁₅N₅O₄ 
• 13472-00-9 p-Aminophenethylamine 
• 1453299-76-7 4-bromo-5-(4-methoxyphenyl)-1-(4-nitrophenethyl)-1H-1,2,3-triazole 
• 1453299-97-2 2-(4-bromo-1-(4-nitrophenethyl)-1H-1,2,3-triazol-5-yl)propan-2-ol 
• 1453299-91-6 4-bromo-1-(4-nitrophenethyl)-5-(thiophen-3-yl)-1H-1,2,3-triazole 
• 1453299-88-1 3-(4-bromo-1-(4-nitrophenethyl)-1H-1,2,3-triazol-5-yl)phenol 

Relevant articles and documents

Sustainable organophosphorus-catalysed Staudinger reduction

A highly efficient and sustainable catalytic Staudinger reduction for the conversion of organic azides to amines in excellent yields has been developed. The reaction displays excellent functional group tolerance to functionalities that are otherwise prone to reduction, such as sulfones, esters, amides, ketones, nitriles, alkenes, and benzyl ethers. The green nature of the reaction is exemplified by the use of PMHS, CPME, and a lack of column chromatography.

Copper complexes bearing an NHC-calixarene unit: Synthesis and application in click chemistry

The synthesis of N-heterocyclic carbene (NHC) copper complexes supported by calix[4]arene is reported. Mono-substituted calix[4]arene was prepared through conventional procedures, followed by the attachment of an imidazolyl group to create the precursor o

Direct C-H amination of arenes with alkyl azides under rhodium catalysis

New horizons in the utility of azides: The rhodium-catalyzed intermolecular direct C-H amination of arenes with alkyl azides provides a convenient route to N-alkyl anilines (see scheme; DG=directing group). Alkyl azides with a wide range of functional groups reacted readily with various substrates, including benzamides, aromatic ketones, and flavones. Copyright