Propanoic acid, 2-iodo-, ethyl ester, also known as ethyl 2-iodopropanoate, is an organic compound characterized by its ester functional group derived from propanoic acid and ethanol. It features a propanoic acid backbone with an iodine atom substituted at the second carbon position. This compound typically appears as a colorless to pale yellow liquid with a fruity odor. It is soluble in organic solvents and exhibits moderate polarity due to the presence of the ester group. The presence of the iodine atom can impart unique reactivity, making it useful in various organic synthesis applications, particularly in the formation of carbon-carbon bonds. Additionally, it may exhibit biological activity, which can be of interest in pharmaceutical research. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if ingested or inhaled. Proper storage conditions are also essential to maintain its stability and prevent degradation.

Propanoic acid, 2-iodo-, ethyl ester

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Ethyl 2-Iodopropionate

ETHYL 2-IODOPROPIONATE

Ethyl 2-iodopropionate is a model complex that can be prepared in a single step. It is a monomer with an hydroxyl group and a crystallography of C2/c. Ethyl 2-iodopropionate has been used to study the interaction between organometallic complexes and metal ions, as well as the voltammetric response of these complexes. The crystal structure of ethyl 2-iodopropionate has been studied by X-ray diffraction methods at 100 K. The crystal lattice contains two molecules per unit cell, each molecule consisting of one ethyl group and one iodine atom.

CAS 31253-08-4: Propanoic acid, 2-iodo-, ethyl ester

Ethyl 2-Iodopropionate

Ref: 54-OR1013156

Ethyl 2-Iodopropionate

Ref: 3B-E1198

ETHYL 2-IODOPROPIONATE

Ref: IN-DA00BDO8

Ethyl 2-Iodopropionate

Ref: 10-F626681

Ethyl 2-Iodopropionate

Ref: 3D-GBA25308