CAS 2401-21-0
:1,2-Dichloro-3-iodobenzene
Description:
1,2-Dichloro-3-iodobenzene is an organic compound characterized by a benzene ring substituted with two chlorine atoms and one iodine atom. The specific positions of these substituents on the aromatic ring are crucial, as they influence the compound's reactivity and physical properties. This compound typically appears as a colorless to pale yellow liquid or solid, depending on the temperature. It is known for its moderate solubility in organic solvents and limited solubility in water. The presence of halogen atoms contributes to its potential applications in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, 1,2-Dichloro-3-iodobenzene may exhibit biological activity, making it of interest in medicinal chemistry and agrochemical research. Safety considerations are important when handling this compound, as it may pose health risks due to its halogenated nature, which can lead to environmental persistence and toxicity. Proper storage and disposal methods should be followed to mitigate any potential hazards associated with its use.
Formula:C6H3Cl2I
InChI:InChI=1S/C6H3Cl2I/c7-4-2-1-3-5(9)6(4)8/h1-3H
InChI key:InChIKey=VGJKBWPZBVBXGI-UHFFFAOYSA-N
SMILES:ClC1=C(Cl)C=CC=C1I
Synonyms:- 1,2-Dichloro-3-Iodobenzene
- 1-Iodo-2,3-dichlorobenzene
- 2,3-Dichloriodobenzene
- 2,3-Dichloro-1-iodobenzene
- 2,3-Dichlorophenyl iodide
- Benzene, 1,2-dichloro-3-iodo-
- 2,3-Dichloroiodobenzene
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Found 5 products.
1,2-Dichloro-3-iodobenzene
CAS:Formula:C6H3Cl2IPurity:98%Color and Shape:SolidMolecular weight:272.89851,2-Dichloro-3-iodobenzene
CAS:<p>1,2-Dichloro-3-iodobenzene</p>Purity:98%Color and Shape:White-Pale Yellow PowderMolecular weight:272.90g/mol1,2-Dichloro-3-iodobenzene
CAS:Formula:C6H3Cl2IPurity:98%Color and Shape:SolidMolecular weight:272.891,2-Dichloro-3-iodobenzene
CAS:<p>Iodobenzene is a chemical compound that is composed of two benzene rings joined by a single bond. Iodobenzene isomers are also called iodosobenzenes and they contain one or more chlorine atoms. Iodobenzene has been shown to have anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis. Iodobenzene inhibits the enzyme phospholipase A2, which is involved in the production of prostaglandins. Iodobenzene binds to enzymes by forming a covalent bond with an electron-rich atom such as oxygen, nitrogen or sulfur in the active site of the enzyme. This type of inhibition is called non-nucleoside inhibition because it does not require an intermediate molecule such as ATP or NADH for binding to the enzyme. Carbonyl groups on iodobenzene molecules form strong bonds with nucleophilic groups on enzymes, leading to enzyme inhibition and</p>Formula:C6H3Cl2IPurity:Min. 95%Molecular weight:272.9 g/mol1,2-Dichloro-3-iodobenzene
CAS:Formula:C6H3Cl2IPurity:>98.0%(GC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:272.89




