2-Chloro-6-iodotoluene is an organic compound characterized by the presence of both chlorine and iodine substituents on a toluene ring. It features a chloromethyl group at the second position and an iodomethyl group at the sixth position of the aromatic ring. This compound is typically a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. It is known for its moderate solubility in organic solvents, such as ethanol and ether, while being less soluble in water due to its hydrophobic aromatic structure. The presence of halogens (chlorine and iodine) contributes to its reactivity, making it useful in various chemical synthesis processes, including the production of pharmaceuticals and agrochemicals. Additionally, 2-chloro-6-iodotoluene can undergo nucleophilic substitution reactions, which are common in organic chemistry. Safety precautions should be taken when handling this compound, as it may pose health risks, including irritation to the skin and eyes, and potential environmental hazards.

2-Chloro-6-iodotoluene

42048-11-3: 1-Chloro-3-iodo-2-methylbenzene, 2-Iodo-6-chlorotoluene

2-Chloro-6-iodotoluene is a racemic mixture of 2-chloro-6-iodotoluene and its antipode, 2-chloro-6-iodotoluene. This compound is used to synthesize heterocycles and biphenyls. It has been shown to be an effective alkylating agent in the presence of ultraviolet light.
2CIT is a colorless liquid with a strong smell. It has UV absorption maxima at 221 nm, 254 nm, and 306 nm.

CAS 42048-11-3: 2-Chloro-6-iodotoluene

2-Chloro-6-iodotoluene

Ref: 10-F018382

2-Chloro-6-iodotoluene

Ref: 3D-FC64653

2-Chloro-6-iodotoluene

Ref: IN-DA003B7F

2-Chloro-6-iodotoluene

Ref: 54-OR2869

2-Chloro-6-iodotoluene

Ref: 3B-C1603