4531-79-7

Basic information

• Product Name: 3-NITRODIPHENYLAMINE
• Synonyms: 3-NITRODIPHENYLAMINE;3-Nitro-N-phenylbenzenamine;3-nitro-N-phenylaniline;BenzenaMine, 3-nitro-N-phenyl-
• CAS NO: 4531-79-7
• Molecular Formula: C₁₂H₁₀N₂O₂
• Molecular Weight: 214.22
• Mol File: 4531-79-7.mol
• Article Data: 42

Chemical Properties

• Boiling Point: 359.3°Cat760mmHg
• Flash Point: 171.1°C
• Appearance: /
• Density: 1.28g/cm³
• Vapor Pressure: 2.39E-05mmHg at 25°C
• Refractive Index: 1.665
• CAS DataBase Reference: 3-NITRODIPHENYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-NITRODIPHENYLAMINE(4531-79-7)
• EPA Substance Registry System: 3-NITRODIPHENYLAMINE(4531-79-7)

Safety Data

• Hazardous Substances Data: 4531-79-7(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H10N2O2/c15-14(16)12-8-4-7-11(9-12)13-10-5-2-1-3-6-10/h1-9,13H

Upstream product

• 27693-70-5 N-(3-nitrophenyl)anthranilic acid 
• 108-86-1 bromobenzene 
• 99-09-2 3-nitro-aniline 
• 99-65-0 meta-dinitrobenzene 
• 100-59-4 phenylmagnesium chloride 
• 585-79-5 m-nitrobromobenzene 
• 62-53-3 aniline 
• 13331-27-6 m-nitrobenzene boronic acid 
• 591-50-4 iodobenzene 
• 98-80-6 phenylboronic acid 
• 645-00-1 m-iodonitrobenzene 
• 639-58-7 triphenyltin chloride 
• 1516-59-2 3-nitrophenyl azide 
• 108-90-7 chlorobenzene 

Downstream Products

• 5840-03-9 N-phenyl-1,3-benzenediamine 
• 91494-11-0 (3-nitro-phenyl)-nitroso-phenyl-amine 
• 32047-90-8 N-(3-nitro-phenyl)-N-phenyl-acetamide 
• 37711-28-7 Diphenylamino-carbaminsaeure-3-aethylester 
• 37711-29-8 Phenothiazine-2-carbamic acid ethyl ester 
• 581-29-3 acridin-3-ylamine 
• 32426-48-5 N-(3-amino-phenyl)-N-phenyl-acetamide 
• 19619-91-1 N-[3-(phenylamino)phenyl]acetamide 
• 861058-84-6 N-phenyl-N,N'-m-phenylene-bis-acetamide 
• 879127-21-6 N-(3-aminophenyl)-cyclopropanecarboxamide 
• 101946-39-8 N-(3-nitrophenyl) cyclopropanecarboxamide 
• 49868-39-5 3-Anilinotrifluormethansulfonanilid 
• 118989-59-6 N-(3-nitrophenyl)-N-phenyl-2-(4-methyl-1-piperazinyl)acetamide 
• 118989-61-0 N-(3-nitrophenyl)-N-phenyl-2-chloroacetamide 

Relevant articles and documents

HETEROCYCLIC COMPOUNDS FOR MODULATING NR2F6

The present disclosure relates to compounds capable of modulating the activity of NR2F6. The compounds of the disclosure may be used in methods for the prevention and/or the treatment of diseases and disorders associated with modulating NR2F6 activity.

Growing the molecular architecture of imidazole-like ligands in HO-1 complexes

Up-regulation of HO-1 had been frequently reported in different cases and types of human malignancies. Since poor clinical outcomes are reported in these cases, this enzyme's inhibition is considered a valuable and proven anticancer approach. To identify

Synthesis and characterization of new square planar heteroleptic cationic complexes [Ni(ii) β-oxodithioester-dppe]+; Their use as a catalyst for Chan-Lam coupling

Novel heteroleptic [Ni(ii) β-oxodithioester-dppe]+PF6- complexes (β-oxodithioester = methyl-3-hydroxy-3-benzyl-2-propenedithioate L1 1, methyl-3-hydroxy-3-(p-methoxyphenyl)-2-propenedithioate L2 2, methyl-3-hydroxy-3-(naphthyl)-2-propenedithioate L3 3, methyl-3-hydroxy-3-(p-chlorophenyl)-2-propenedithioate L4 4, methyl-3-hydroxy-3-(p-bromophenyl)-2-propenedithioate L5 5 and methyl-3-hydroxy-3-(p-cyanophenyl)-2-propenedithioate L6 6) have been synthesized and characterized by elemental (C, H, N) analysis, ESI-MS, IR, UV-visible, 1H, 13C{1H}, 31P{1H} and 19F{1H} NMR spectroscopy. The distorted square planar structures of the isomorphous cationic complexes 2, 3, 4 and 5 have been determined by X-ray crystallography. The catalytic activities of 1-6 were investigated for the Chan-Lam coupling reaction involving arylboronic acids and amines to afford N-arylated products in good to excellent yields under mild conditions with 1 mol% catalyst loading. This catalytic protocol offers significant functional group tolerance, and is endowed with a broad substrate scope. This journal is