958-96-3

Basic information

• Product Name: 3,3'-DINITRO-BIPHENYL
• Synonyms: 3,3'-DINITRO-BIPHENYL;3,3'-Dinitro-1,1'-biphenyl;1-nitro-3-(3-nitrophenyl)benzene
• CAS NO: 958-96-3
• Molecular Formula: C₁₂H₈N₂O₄
• Molecular Weight: 244.20292
• Mol File: 958-96-3.mol
• Article Data: 24

Chemical Properties

• Boiling Point: 416°Cat760mmHg
• Flash Point: 207.4°C
• Appearance: /
• Density: 1.368g/cm³
• CAS DataBase Reference: 3,3'-DINITRO-BIPHENYL(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3'-DINITRO-BIPHENYL(958-96-3)
• EPA Substance Registry System: 3,3'-DINITRO-BIPHENYL(958-96-3)

Safety Data

• Hazardous Substances Data: 958-96-3(Hazardous Substances Data)

Upstream product

• 2453-41-0 3-nitroperbenzoic acid 
• 65-85-0 benzoic acid 
• 586-36-7 3-nitrophenyldiazonium tetrafluoroborate 
• 1104877-48-6 4-bromo-2-(2-iodo-phenoxy)methyl-1-(prop-1-ynyl)benzene 
• 13331-27-6 m-nitrobenzene boronic acid 
• 645-00-1 m-iodonitrobenzene 
• 90-14-2 1-Iodonaphthalene 
• 1679-18-1 4-Chlorophenylboronic acid 
• 5570-18-3 2-aminophenylboronic acid 
• 6165-68-0 thiophene boronic acid 
• 13331-23-2 fur-2-ylboronic acid 
• 98437-24-2 benzofuran-2-boronic acid 
• 100622-34-2 anthracene-9-boronic acid 
• 164461-18-1 1-pyrenylboronic acid 

Downstream Products

• 106323-83-5 3,4,3'-Trinitro-biphenyl 
• 136905-61-8 N³,N³,N^3',N^3'-Tetrakis-(4-methoxy-phenyl)-biphenyl-3,3'-diamine 
• 31835-64-0 3-amino-3'-nitrobiphenyl 
• 128923-93-3 1‐(3‐methoxyphenyl)‐3‐nitrobenzene 

Relevant articles and documents

An Active Palladium Colloidal Catalyst for the Selective Oxidative Heterocoupling of (Hetero)Aryl Boronic Acids

A highly selective oxidative heterocoupling protocol for (hetero)aryl boronic acids with an active palladium colloidal catalyst was developed. The judicious choice of electronically different aryl boronic acids made possible such couplings under mild conditions, with air as oxidant, while embracing a wide substrate scope. This successful approach further allowed the development of a unique one-pot sequential oxidative heterocoupling/Suzuki–Miyaura cross-coupling tandem process for accessing substituted terphenyls.

A deacetylation-diazotation-coupling sequence: Palladium-catalyzed C-C bond formation with acetanilides as formal leaving groups

Acetanilides can be deacetylated and diazotized in situ, and subsequently used in Pd-catalyzed coupling reactions without isolation of the diazonium intermediate. Heck reactions, Suzuki crosscoupling reactions, and a Pd-catalyzed [2+2+1] cycloaddition hav

Homocoupling of arylboronic acids catalyzed by CuCl in air at room temperature

Homocoupling of arylboronic acids has been successfully carried out by using the inexpensive simple copper salt CuCl as the catalyst in methanol to obtain symmetric biaryls in good to excellent yields. The reaction proceeds with a CuCl loading of 2 mol-% under extremely mild conditions: in air, at room temperature, without the need of any additives such as base, oxidant, or ligand. A simple and efficient CuCl-catalyzed homocoupling of arylboronic acids for the synthesis of symmetrical biaryls is described. The homocoupling reaction takes place with a catalyst loading of at 2 mol-% in economical and easily handled methanol and under extremely mild conditions: in air, at room temperature, without any additives such as base, oxidant, or ligand. Copyright