CAS 67832-11-5
:4-Bromo-2-methylbenzonitrile
Description:
4-Bromo-2-methylbenzonitrile is an organic compound characterized by its aromatic structure, which includes a bromine atom and a nitrile functional group. It features a benzene ring substituted with a bromine atom at the para position and a methyl group at the ortho position relative to the nitrile group. This compound is typically a solid at room temperature and is known for its moderate solubility in organic solvents such as ethanol and acetone, while being less soluble in water due to its hydrophobic aromatic nature. The presence of the nitrile group contributes to its reactivity, making it useful in various chemical syntheses and applications in pharmaceuticals and agrochemicals. Additionally, the bromine substituent can facilitate further chemical modifications, such as nucleophilic substitutions. Safety data indicates that, like many brominated compounds, it should be handled with care due to potential toxicity and environmental concerns. Overall, 4-Bromo-2-methylbenzonitrile is a valuable compound in organic synthesis and research.
Formula:C8H6BrN
InChI:InChI=1/C8H6BrN/c1-6-4-8(9)3-2-7(6)5-10/h2-4H,1H3
SMILES:Cc1cc(ccc1C#N)Br
Synonyms:- 4-BROMO-2-METHYLBENZONITRILE
- 4-Bromo-2-Methylbenzonitrile97%
- TIMTEC-BB SBB005832
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Found 5 products.
4-Bromo-2-methylbenzonitrile
CAS:Formula:C8H6BrNPurity:>98.0%(GC)Color and Shape:White to Light yellow powder to crystalineMolecular weight:196.054-Bromo-2-methylbenzonitrile
CAS:Formula:C8H6BrNPurity:97%Color and Shape:SolidMolecular weight:196.04394-Bromo-2-methylbenzonitrile
CAS:<p>4-Bromo-2-methylbenzonitrile</p>Formula:C8H6BrNPurity:≥95%Color and Shape: off-white to pale lemon solidMolecular weight:196.04g/mol4-Bromo-2-methylbenzonitrile
CAS:Formula:C8H6BrNPurity:97%Color and Shape:SolidMolecular weight:196.0474-Bromo-2-methylbenzonitrile
CAS:<p>4-Bromo-2-methylbenzonitrile (4BMB) is a biphenyl derivative that inhibits the activity of tyrosine kinase enzymes. It has been shown to be a virulence factor for Streptococcus, which causes lysis of red blood cells. 4BMB has also been shown to inhibit the growth of Escherichia coli and other bacteria, including Streptococcus pneumoniae, by inducing cell lysis. The mechanism of action for this drug is through binding to an anion in the active site, causing reversible inhibition of ATP synthase. This causes an increase in intracellular pH and leads to cell death. 4BMB is fluorescent under UV light and can be used as a molecular probe for studying hydrogen bond formation and interactions with anions.</p>Formula:C8H6BrNPurity:Min. 95%Color and Shape:PowderMolecular weight:196.04 g/mol




