CAS 83553-47-3

4-Thiazolecarboxylic acid, 2-iodo-, ethyl ester

Description:

4-Thiazolecarboxylic acid, 2-iodo-, ethyl ester is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. This compound features a carboxylic acid functional group and an ethyl ester moiety, contributing to its reactivity and solubility properties. The presence of the iodine atom at the 2-position of the thiazole ring enhances its potential for nucleophilic substitution reactions, making it a valuable intermediate in organic synthesis. Typically, compounds like this exhibit moderate to high polarity due to the carboxylic acid and ester functionalities, which can influence their solubility in various solvents. Additionally, the thiazole ring can participate in various chemical reactions, including electrophilic aromatic substitution and coordination with metal ions. This compound may find applications in pharmaceuticals, agrochemicals, or as a building block in the synthesis of more complex molecules. Safety data should be consulted for handling and storage, as halogenated compounds can pose specific health and environmental risks.

Formula: C₆H₆INO₂S

Ethyl 2-iodo-1,3-thiazole-4-carboxylate

CAS: 83553-47-3

Ethyl 2-iodo-1,3-thiazole-4-carboxylate is a crystalline polymer that is produced from ethyl cyanoacetate. It functions as a copolymer when combined with other monomers and has been used to produce semiconducting materials in transistors. In addition, it can be used as an electron donor in organic solar cells and electron deficient conductors for transport devices. Ethyl 2-iodo-1,3-thiazole-4-carboxylate has been shown to be unipolar, which means that it only carries electric current in one direction.

Formula: C₆H₆INO₂S

Purity: Min. 95%

Molecular weight: 283.09 g/mol

Ref: 3D-IDA55347