34862-87-8

Basic information

• Product Name: 2AMINO3NITROBIPHENYL
• Synonyms: 3'-Nitrobiphenyl-2-amine;2-(3-nitrophenyl)aniline
• CAS NO: 34862-87-8
• Molecular Formula: C₁₂H₁₀N₂O₂
• Molecular Weight: 214.22
• Mol File: 34862-87-8.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 384.6°Cat760mmHg
• Flash Point: 186.4°C
• Appearance: /
• Density: 1.268g/cm³
• CAS DataBase Reference: 2AMINO3NITROBIPHENYL(CAS DataBase Reference)
• NIST Chemistry Reference: 2AMINO3NITROBIPHENYL(34862-87-8)
• EPA Substance Registry System: 2AMINO3NITROBIPHENYL(34862-87-8)

Safety Data

• Hazardous Substances Data: 34862-87-8(Hazardous Substances Data)

Usage

General Description

2-Amino-3-nitrobiphenyl is a chemical compound with the molecular formula C12H10N2O2. It is an aromatic amine with a nitro group attached to one of the benzene rings. This chemical is classified as a Group 2A carcinogen by the International Agency for Research on Cancer (IARC) and is considered to be a potential human carcinogen. It is primarily used in research and experimental purposes to study its carcinogenic effects and its potential as a mutagen. Exposure to 2-Amino-3-nitrobiphenyl has been linked to an increased risk of developing bladder and liver cancer, and it is important to handle and use this chemical with extreme caution in a laboratory setting.

Upstream product

• 13331-27-6 m-nitrobenzene boronic acid 
• 5570-18-3 2-aminophenylboronic acid 
• 615-36-1 2-bromoaniline 
• 615-43-0 2-iodophenylamine 

Downstream Products

• 1330574-31-6 ethyl 2-(5,6-dihydro-9-nitro-5-tosylphenanthridin-6-yl)acetate 
• 1312448-07-9 N-Ts-2-(3'-nitrophenyl)aniline 
• 81316-78-1 1-nitrotriphenylene 
• 81316-79-2 2-nitrotriphenylene 
• 289480-22-4 trans-4-[9-ethyl-6-(3-nitro-phenylamino)-9H-purin-2-yl-amino]cyclohexanol 

Relevant articles and documents

Intramolecular Remote C-H Activation via Sequential 1,4-Palladium Migration to Access Fused Polycycles

An unprecedented intramolecular remote C-H activation via sequential 1,4-palladium migration with an aromatic ring as a conveyor has been described. This reaction provides an efficient route to construct diverse polycyclic frameworks in moderate to good yield via palladium-catalyzed remote C-H activation/alkene insertion, arylation, alkenylation, and the Heck reaction. The preliminary mechanistic studies revealed that the 1,4-palladium migration process was reversible.

Derivative of triaromatic amines and organic electroluminescence device thereof

The invention discloses a derivative of triaromatic amines and organic electroluminescent device thereof, which relates to the technical field of organic photoelectric material, the derivative of triaromatic amines provided by the invention has bipolar structure, which has good carrier transport characteristics so that electrons and holes can be effectively combined in the luminescent layer, the luminescent efficiency is high. In addition, the derivative of triaromatic amines provided by the invention has relatively high vitrification temperature and thermal stability, which is helpful for material film formation. The electroluminescence device provided by the invention includes a cathode, an anode and one or more organics layers, at least one organic layer contains derivatives of triaromatic amines provided by the invention, the organic electroluminescence device provided by the invention has relatively low driving voltage, relatively high luminous efficiency and luminosity and relatively long service life.

Palladium-catalyzed interannular meta-C-H arylation

The interannular meta-selective C-H arylation of biaryl-2-trifluoroacetamides using Pd(ii)/norbornene catalysis is reported. The installation of a trifluoroacetyl protecting group to tune their electronic properties and binding ability is essential for in