19613-87-7

Basic information

• Product Name: N-hydroxy-2-nitroaniline
• Synonyms: Benzenamine, N-hydroxy-2-nitro-; Hydroxylamine, N-(o-nitrophenyl)-; N-(o-Nitrophenyl)hydroxylamine
• CAS NO: 19613-87-7
• Molecular Formula: C₆H₆N₂O₃
• Molecular Weight: 154.1234
• Mol File: 19613-87-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 313.4°C at 760 mmHg
• Flash Point: 143.3°C
• Density: 1.514g/cm³
• Vapor Pressure: 0.000212mmHg at 25°C
• Refractive Index: 1.699
• CAS DataBase Reference: N-hydroxy-2-nitroaniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-hydroxy-2-nitroaniline(19613-87-7)
• EPA Substance Registry System: N-hydroxy-2-nitroaniline(19613-87-7)

Safety Data

• Hazardous Substances Data: 19613-87-7(Hazardous Substances Data)

Upstream product

• 528-29-0 1,2-Dinitrobenzene 
• 67-64-1 acetone 
• 50-81-7 ascorbic acid 
• 612-29-3 o-nitronitrosobenzene 
• 88-74-4 2-nitro-aniline 

Downstream Products

• 480-96-6 benzofurazan oxide 
• 88-74-4 2-nitro-aniline 
• 127526-86-7 N-benzoyloxy-2-nitrobenzenamine 
• 127526-87-8 N-benzoyl-N-benzoyloxy-2-nitrobenzenamine 
• 127526-88-9 N-(4'-nitrobenzoyloxy)-2-nitrobenzenamine 
• 95-54-5 1,2-diamino-benzene 
• 612-29-3 o-nitronitrosobenzene 
• 728-90-5 N-(2-nitrophenyl)benzanilide 

Relevant articles and documents

Highly selective and controllable synthesis of arylhydroxylamines by the reduction of nitroarenes with an electron-withdrawing group using a new nitroreductase BaNTR1

A new bacterial nitroreductase has been identified and used as a biocatalyst for the controllable reduction of a variety of nitroarenes with an electron-withdrawing group to the corresponding N-arylhydroxylamines under mild reaction conditions with excellent selectivity (>99%). This method therefore represents a green and efficient method for the synthesis of arylhydroxylamines.

Carbon supported Pt colloid as effective catalyst for selective hydrogenation of nitroarenes to arylhydroxylamines

The Pt colloid supported on carbon is an active and selective catalyst for the partial hydrogenation of nitroaromatics with electron-withdrawing substituents to the corresponding N-arylhydroxylamine, indicating an additive-free green catalytic approach fo

A novel strategy for the preparation of arylhydroxylamines: Chemoselective reduction of aromatic nitro compounds using bakers' yeast

Using bakers' yeast as a biocatalyst, the chemoselective reduction of aromatic nitro compounds bearing electron-withdrawing groups gave the corresponding hydroxylamines with good to excellent conversion under mild conditions.