CAS 69113-59-3
:3-Iodobenzonitrile
Description:
3-Iodobenzonitrile, with the CAS number 69113-59-3, is an organic compound characterized by the presence of both an iodine atom and a nitrile group attached to a benzene ring. Specifically, the iodine atom is located at the meta position relative to the nitrile group, which is a cyano (-C≡N) functional group. This compound typically appears as a white to light yellow solid and is known for its aromatic properties due to the benzene ring. It is relatively insoluble in water but soluble in organic solvents such as acetone and dichloromethane. 3-Iodobenzonitrile is often utilized in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals, due to its reactivity and ability to participate in nucleophilic substitution reactions. Additionally, the presence of the iodine atom can facilitate further functionalization, making it a valuable intermediate in synthetic chemistry. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested.
Formula:C7H4IN
InChI:InChI=1/C7H4IN/c8-7-3-1-2-6(4-7)5-9/h1-4H
SMILES:c1cc(cc(c1)I)C#N
Synonyms:- 3-Cyano-1-iodobenzene
- m-Iodobenzonitrile
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Found 6 products.
3-Iodobenzonitrile
CAS:Formula:C7H4INPurity:>98.0%(GC)Color and Shape:White to Light yellow to Dark green powder to crystalMolecular weight:229.023-Iodobenzonitrile
CAS:<p>3-Iodobenzonitrile</p>Formula:C7H4INPurity:98%Color and Shape: orange/tan chunks & crystalsMolecular weight:229.02g/molm-Iodobenzonitrile
CAS:<p>m-Iodobenzonitrile is a chemical reagent that is a hydrogen bond acceptor and donor. It has been used for the analysis of dopamine, tosylates, and carbonyl compounds. It can also be used in kinetic studies of hydrogen bonding interactions. The dipole moment of m-iodobenzonitrile is 1.779 D. The transport properties of m-iodobenzonitrile are negligible due to its low vapor pressure. Kinetic studies have shown that it reacts with hydrogen gas at room temperature to form a dipole ion pair with an estimated rate constant of 6x10 M/sec. Cross-coupling reactions with aryl halides have been observed at room temperature in the presence of copper catalyst and sodium bicarbonate buffer. Analytical chemistry has shown that m-iodobenzonitrile reacts with acidic solutions to produce hydrogen ions and carbon dioxide gas.</p>Formula:C7H4INPurity:Min. 95%Color and Shape:PowderMolecular weight:229.02 g/mol3-Iodobenzonitrile
CAS:Controlled Product<p>Applications 3-Iodobenzonitrile<br></p>Formula:C7H4INColor and Shape:Off-WhiteMolecular weight:229.02
