2,2'-DINITROBIPHENYL
2,2'-DINITROBIPHENYL Basic information
- Product Name:
- 2,2'-DINITROBIPHENYL
- Synonyms:
-
- 2,2'-Dinitro-1,1'-biphenyl
- 2,2'-Dinitrobiphenyl, 2,2'-dinitro-
- Biphenyl, 2,2'-dinitro-
- RARECHEM AQ BD 0003
- 1-nitro-2-(2-nitrophenyl)benzene
- 6,6-dinitro-1-phenylcyclohexa-1,3-diene
- 2,2'-DINITROBIPHENYL
- 2,2-DINITROBIPHENYL
- CAS:
- 2436-96-6
- MF:
- C12H8N2O4
- MW:
- 244.2
- EINECS:
- 219-435-4
- Product Categories:
-
- Aromatic Hydrocarbons (substituted) & Derivatives
- Building Blocks
- Chemical Synthesis
- Nitro Compounds
- Nitrogen Compounds
- Organic Building Blocks
- Biphenyls (for High-Performance Polymer Research)
- Functional Materials
- Reagent for High-Performance Polymer Research
- Nitro Compounds
- Nitrogen Compounds
- Organic Building Blocks
- Mol File:
- 2436-96-6.mol
2,2'-DINITROBIPHENYL Chemical Properties
- Melting point:
- 124-126 °C(lit.)
- Boiling point:
- 305°C
- Density
- 1,45 g/cm3
- refractive index
- 1.6360 (estimate)
- Flash point:
- 305°C
- storage temp.
- Sealed in dry,2-8°C
- form
- powder to crystal
- color
- White to Light yellow
- Water Solubility
- Insoluble in water
- BRN
- 1579851
- CAS DataBase Reference
- 2436-96-6(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
2,2'-DINITROBIPHENYL Usage And Synthesis
Chemical Properties
light yellow to beige crystalline powder
Uses
2,2?-Dinitrobiphenyl has been used as an internal standard in the determination of p,p?-DDT in technical and formulated products using gas chromatographic method
Uses
2,2′-Dinitrobiphenyl has been used as an internal standard in the determination of p,p′-DDT in technical and formulated products using gas chromatographic method.
Definition
ChEBI: Biphenyl substituted with nitro groups at the 2- and 2'-positions.
Synthesis Reference(s)
Organic Syntheses, Coll. Vol. 3, p. 339, 1955
The Journal of Organic Chemistry, 53, p. 4482, 1988 DOI: 10.1021/jo00254a012
Tetrahedron Letters, 16, p. 143, 1975
General Description
The electroreduction of 2,2′-dinitrobiphenyl in anionic, cationic, and nonionic micellar solutions has been studied by polarography and cyclic voltammetry.
Purification Methods
Crystallise the biphenyl from EtOH, AcOH (m 124.5o) or pet ether (m 125.5-126o). [Beilstein 5 H 538, 5 III 1759, 5 IV 1826.]
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