CAS 92-93-3
:4-Nitro-1,1′-biphenyl
Description:
4-Nitro-1,1′-biphenyl, with the CAS number 92-93-3, is an organic compound characterized by its biphenyl structure substituted with a nitro group at the para position. This compound typically appears as a yellow crystalline solid and is known for its aromatic properties, which contribute to its stability and reactivity. It has a relatively high melting point and is soluble in organic solvents such as ethanol and acetone, but has limited solubility in water. The presence of the nitro group introduces significant electron-withdrawing characteristics, influencing its chemical reactivity and making it a useful intermediate in organic synthesis, particularly in the production of dyes and pharmaceuticals. Additionally, 4-nitro-1,1′-biphenyl can undergo various reactions, including electrophilic substitution and reduction, which are important in synthetic organic chemistry. However, it is essential to handle this compound with care due to potential toxicity and environmental concerns associated with nitroaromatic compounds.
Formula:C12H9NO2
InChI:InChI=1S/C12H9NO2/c14-13(15)12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H
InChI key:InChIKey=BAJQRLZAPXASRD-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=CC=C(C=C1)C2=CC=CC=C2
Synonyms:- 1,1′-Biphenyl, 4-nitro-
- 1-Nitro-4-phenylbenzene
- 4-(4-Nitrophenyl)benzene
- 4-Nitrobifenilo
- 4-Nitrobiphenyl
- 4-Nitrobiphenyle
- 4-Nitrodifenilo
- 4-Nitrodiphenyl
- 4-Phenylnitrobenzene
- Ba 2794
- Biphenyl, 4-nitro-
- Nsc 1324
- p-Nitrobiphenyl
- p-Nitrodiphenyl
- p-Phenylnitrobenzene
- 4-Nitro-1,1′-biphenyl
- See more synonyms
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Found 5 products.
4-Nitrobiphenyl 10 µg/mL in Cyclohexane
CAS:Controlled ProductFormula:C12H9NO2Color and Shape:Single SolutionMolecular weight:199.214-Nitrobiphenyl
CAS:<p>4-Nitrobiphenyl</p>Formula:C12H9NO2Purity:97%Color and Shape: off white to faint yellow solidMolecular weight:199.21g/mol4-Nitrobiphenyl
CAS:Controlled Product<p>4-Nitrobiphenyl is a nitro compound that has been shown to have anthelmintic activity against the nematode, Typhimurium. The mechanism of action for 4-nitrobiphenyl is not known, but it may inhibit the acetate extract of the parasite and reduce its growth rate. 4-Nitrobiphenyl also inhibits the enzyme activities in bladder cells, which may be due to its ability to target tissue. It has also been shown to have no effect on untreated control cells. There are many chemical reactions that occur when 4-nitrobiphenyl is exposed to microbes, including biphenyl and ether formation and dehydroascorbate reductase inhibition.</p>Formula:C12H9NO2Purity:Min. 94 Area-%Color and Shape:PowderMolecular weight:199.21 g/mol



