CAS 615-41-8

o-chlroiodobenzene

Description:

o-Chloroiodobenzene, with the CAS number 615-41-8, is an aromatic halogenated compound characterized by the presence of both chlorine and iodine substituents on a benzene ring. Specifically, the chlorine atom is located in the ortho position relative to the iodine atom, which influences its chemical reactivity and physical properties. This compound typically appears as a colorless to pale yellow liquid and has a relatively high boiling point due to the presence of halogen atoms, which increase molecular weight and intermolecular forces. o-Chloroiodobenzene is known for its utility in organic synthesis, particularly in the formation of carbon-carbon bonds and as a reagent in various coupling reactions. It exhibits moderate toxicity and should be handled with care, as exposure can lead to health risks. Additionally, it is important to consider its environmental impact, as halogenated compounds can be persistent in the environment. Proper storage and disposal methods are essential to mitigate any potential hazards associated with this chemical.

Formula: C₆H₄ClI

InChI: InChI=1/C6H4ClI/c7-5-3-1-2-4-6(5)8/h1-4H

InChI key: InChIKey=MPEOPBCQHNWNFB-UHFFFAOYSA-N

SMILES: ClC1=C(I)C=CC=C1

Synonyms:

• 1-Chloro-2-Iodobenzene
• 1-Iodo-2-chlorobenzene
• 2-Chloro-1-iodobenzene
• 2-Chloroiodobenzene
• 2-Chlorophenyl iodide
• 2-Iodochlorobenzene
• 2-Iodophenyl chloride
• Benzene, 1-chloro-2-iodo-
• NSC 32860
• O-Iodochlorobenzene
• o-Chloroiodobenzene
• o-Chlorophenyl iodide
• 1-chloro-2-iodo-benzen
• 1-Chloro-2-iodobenzene,99%
• 2-Chloroiodobenzene (stabilized with Copper chip)
• 2-Chloroiodobenzene 97%

1-Chloro-2-iodobenzene (stabilized with Copper chip)

CAS: 615-41-8

Formula: C₆H₄ClI

Purity: >98.0%(GC)

Color and Shape: Colorless to Yellow to Green clear liquid

Molecular weight: 238.45

Ref: 3B-C0189

1-Chloro-2-iodobenzene, 99%

CAS: 615-41-8

1-Chloro-2-iodobenzene is used as a precursor and involved in the preparation of 2,2'-dichloro-biphenyl. It is also used to prepare N,N-diaryl-o-phenylenediamines and 4(5)-(2-chlorophenyl)-1H-imidazole. It reacts with lanthanum metal in the presence of trimethylchlorosilane to prepare 1-chloro-2-tr

Formula: C₆H₄ClI

Purity: 99%

Color and Shape: Clear colorless to yellow to orange, Liquid

Molecular weight: 238.45

Ref: 02-A18255

1-chloro-2-iodobenzene

CAS: 615-41-8

Formula: C₆H₄ClI

Purity: 98%

Color and Shape: Liquid

Molecular weight: 238.4534

Ref: IN-DA0032QN

1-Chloro-2-iodobenzene

CAS: 615-41-8

Formula: C₆H₄ClI

Molecular weight: 238.45

Ref: 08-06-0028

2-Chloroiodobenzene

CAS: 615-41-8

2-Chloroiodobenzene

Formula: C₆H₄ClI

Purity: 97%

Color and Shape: clear. colourless liquid

Molecular weight: 238.45g/mol

Ref: 54-OR1893

1-Chloro-2-iodobenzene

CAS: 615-41-8

Formula: C₆H₄ClI

Molecular weight: 238.45

Ref: 7W-GX4334

1-Chloro-2-iodobenzene

CAS: 615-41-8

Formula: C₆H₄ClI

Purity: 98%

Color and Shape: Liquid, Clear

Molecular weight: 238.45

Ref: 10-F001149

o-Iodochlorobenzene

Controlled Product

CAS: 615-41-8

Applications o-Iodochlorobenzene is a building block that has been used as a reactant for the synthesis of biaryl derivatives of seasamol used for their antioxidant activity against DPPH radical.
References Rodriguez, S.A., et. al.: Australian J. Chem., 66, 1334 (2013)

Formula: C₆H₄ClI

Color and Shape: Neat

Molecular weight: 238.45

Ref: TR-I694400

1-Chloro-2-iodobenzene

CAS: 615-41-8

1-Chloro-2-iodobenzene is a chemical that is used in the synthesis of drugs and other organic compounds. It has been shown to be an effective inhibitor of HIV infection, as well as a potent inhibitor of genotoxic activity. 1-Chloro-2-iodobenzene cleaves to form two products: a palladium complex and a copper complex. The reaction products are then subjected to nucleophilic attack by the enzyme human immunodeficiency virus type 1 reverse transcriptase, which results in the formation of an intermediate product with increased stability. This final product inhibits the replication of HIV by binding to the viral DNA polymerase and preventing RNA synthesis. Chemical ionization is used for mass spectrometry analysis, which can identify the peaks corresponding to these products.

Formula: C₆H₄ClI

Purity: Min. 95%

Molecular weight: 238.45 g/mol

Ref: 3D-AAA61541