Methyl 3-iodophenylacetate is an organic compound characterized by its ester functional group, which is formed from the reaction of 3-iodophenylacetic acid and methanol. It typically appears as a colorless to pale yellow liquid with a distinctive aromatic odor. The presence of the iodine atom in its structure contributes to its reactivity and potential applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. This compound is soluble in organic solvents such as ethanol and dichloromethane, while its solubility in water is limited due to its hydrophobic aromatic character. Methyl 3-iodophenylacetate can undergo various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a valuable intermediate in synthetic chemistry. Safety considerations should be taken into account when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate protective measures should be employed. Overall, its unique structural features and reactivity make it a significant compound in the field of organic chemistry.

Methyl 3-iodophenylacetate

502649-73-2:  Benzeneacetic acid, 3-iodo-, methyl ester, methyl 2-(3-iodophenyl)acetate

CAS 502649-73-2: Methyl 3-iodophenylacetate

Methyl 2-(3-iodophenyl)acetate

Ref: 3D-CVA64973

Methyl 2-(3-iodophenyl)acetate

Ref: 54-OR96692

Benzeneacetic acid, 3-iodo-, methyl ester

Ref: IN-DA00I8ZO

METHYL 2-(3-IODOPHENYL)ACETATE

Ref: 10-F534827