CAS 89642-49-9
:4-bromo-3-nitrobenzonitrile
Description:
4-Bromo-3-nitrobenzonitrile is an organic compound characterized by the presence of a bromine atom and a nitro group attached to a benzene ring that also contains a nitrile functional group. Its molecular structure consists of a benzene ring substituted at the 4-position with a bromine atom and at the 3-position with a nitro group, while the nitrile group (-C≡N) is attached to the benzene ring, typically at the 1-position. This compound is known for its potential applications in organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. It is generally a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of both the nitro and bromine substituents can influence its reactivity, making it a useful building block in various chemical reactions, including nucleophilic substitutions and coupling reactions. Safety precautions should be taken when handling this compound, as it may pose health risks due to its chemical nature.
Formula:C7H3BrN2O2
InChI:InChI=1/C7H3BrN2O2/c8-6-2-1-5(4-9)3-7(6)10(11)12/h1-3H
SMILES:c1cc(c(cc1C#N)N(=O)=O)Br
Synonyms:- Benzonitrile, 4-bromo-3-nitro-
- 2-Bromo-5-cyanonitrobenzene
- 4-Bromo-3-nitrobenzonitrile 97%
- 4-BROMO-3-NITROBENZONITRILE ISO 9001:2015 REACH
- 3-nitro-4-broMobenzonitrile
- 4-BROMO-3-NITROBENZONITRILE
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Found 5 products.
4-Bromo-3-nitrobenzonitrile
CAS:Formula:C7H3BrN2O2Purity:>98.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:227.024-Bromo-3-nitrobenzonitrile
CAS:Formula:C7H3BrN2O2Purity:98%Color and Shape:SolidMolecular weight:227.01494-Bromo-3-nitrobenzonitrile
CAS:<p>4-Bromo-3-nitrobenzonitrile</p>Purity:98%Color and Shape:Off-White SolidMolecular weight:227.01g/mol2-Bromo-5-cyanonitrobenzene
CAS:<p>2-Bromo-5-cyanonitrobenzene is a chemical compound that has been shown to have broad-spectrum activity against drug-resistant bacteria. It is able to kill gram-negative and gram-positive bacteria, including drug-resistant strains. The mechanism of action for 2-bromo-5-cyanonitrobenzene is not well understood but it has been observed that the molecule undergoes an oxidative cyclization reaction in the presence of chloride ions or hydroxides. This process leads to the formation of a nitrosobenzene metabolite which reacts with DNA to inhibit protein synthesis and cause cell death. 2-Bromo-5-cyanonitrobenzene has also been shown to be potent against a wide range of different types of bacteria, including those most commonly associated with skin infections, respiratory tract infections, and urinary tract infections.</p>Formula:C7H3BrN2O2Purity:Min. 95%Color and Shape:PowderMolecular weight:227.02 g/mol4-Bromo-3-nitrobenzonitrile
CAS:Formula:C7H3BrN2O2Purity:97%Color and Shape:Solid, White to brown powderMolecular weight:227.017




