Benzenamine, N-hydroxy-3-nitro-

Base Information

• Chemical Name: Benzenamine, N-hydroxy-3-nitro-
• CAS No.: 6418-00-4
• Molecular Formula: C6H6 N2 O3
• Molecular Weight: 154.125
• DSSTox Substance ID: DTXSID80214380
• Nikkaji Number: J509.785A
• Wikidata: Q83090216

Synonyms:N-Hydroxy-3-nitrobenzenamine;Benzenamine, N-hydroxy-3-nitro-;6418-00-4;m-Nitrophenylhydroxylamin;N-Hydroxy-3-nitroaniline;N-(m-nitrophenyl) hydroxylamine;SCHEMBL11445187;DTXSID80214380;VSPZSXLLFMWWLY-UHFFFAOYSA-N

Chemical Property of Benzenamine, N-hydroxy-3-nitro-

Chemical Property:

• Vapor Pressure: 0.000467mmHg at 25°C
• Boiling Point: 301.4°Cat760mmHg
• Flash Point: 136.1°C
• Density: 1.514g/cm³
• XLogP3: 1.4
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 154.03784206
• Heavy Atom Count: 11
• Complexity: 145

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC(=C1)[N+](=O)[O-])NO

Technology Process of Benzenamine, N-hydroxy-3-nitro-

There total 8 articles about Benzenamine, N-hydroxy-3-nitro- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

meta-dinitrobenzene (99-65-0) → N-(3-nitrophenyl)hydroxylamine (6418-00-4)

Guidance literature:

With carbon dioxide; zinc; In water; at 25 ℃; for 0.666667h; under 750.075 Torr; Sonication;

DOI:10.1007/s11164-012-0562-5

Reference yield: 54.0%

meta-dinitrobenzene (99-65-0) → N-(3-nitrophenyl)hydroxylamine (6418-00-4) + 3-nitro-aniline (99-09-2)

Guidance literature:

With 1,2-bis(mercaptomethyl)benzene; (Et4N); In acetonitrile; at 40 ℃; for 6h;

DOI:10.1016/S0040-4039(00)85147-3

Reference yield:

meta-dinitrobenzene (99-65-0) + ethanol (64-17-5) → N-(3-nitrophenyl)hydroxylamine (6418-00-4) + m-phenylenediamine (108-45-2,64554-26-3,76583-20-5) + 3-nitro-aniline (99-09-2)

Guidance literature:

Hydrogenation;

upstream raw materials:

meta-dinitrobenzene

GLUTATHIONE

C₁₆H₂₁N₅O₉S

rac-Ala-OH

Downstream raw materials:

3,3'-dinitro azoxybenzene

1-nitro-3-nitrosobenzene

N-m-nitrophenyl-2-furylacrylohydroxamic acid

N-Hydroxy-N-(3-nitro-phenyl)-benzamide

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