CAS 478239-03-1

4H-Thieno[3,2-b]pyrrole-5-carboxylic acid, 2-methyl-, methyl ester

Description:

4H-Thieno[3,2-b]pyrrole-5-carboxylic acid, 2-methyl-, methyl ester, identified by CAS number 478239-03-1, is a chemical compound that features a thieno-pyrrole core structure, which is characterized by a fused thiophene and pyrrole ring system. This compound typically exhibits properties associated with heterocyclic compounds, including potential biological activity and utility in organic synthesis. The presence of a carboxylic acid moiety, which is esterified to form a methyl ester, suggests that it may participate in various chemical reactions, such as esterification or hydrolysis. The methyl group at the 2-position of the pyrrole ring can influence the compound's solubility and reactivity. Additionally, compounds of this type may be of interest in materials science, particularly in the development of organic semiconductors or photovoltaic materials, due to their electronic properties. Overall, the unique structural features of this compound contribute to its potential applications in pharmaceuticals and advanced materials.

Formula: C₉H₉NO₂S

Methyl 2-methyl-4H-thieno[3,2-b]pyrrole-5-carboxylate

CAS: 478239-03-1

Methyl 2-methyl-4H-thieno[3,2-b]pyrrole-5-carboxylate is a solvent that can be used in the production of other chemicals. It has a number of uses in organic synthesis, including as a chlorinating agent to generate acid chlorides, such as methyl chloroacetate. Methyl 2-methyl-4H-thieno[3,2-b]pyrrole-5-carboxylate is also used in the production of dyes and pharmaceuticals. The methyl ester reacts with hydrogen peroxide to produce an electron and chloride ions. This reaction produces heat and causes the solution to change from colorless to dark blue. The reaction can be catalyzed by various metals, such as copper or iron, or by acid chlorides such as thionyl chloride. The solubility of methyl 2-methyl-4H-thieno[3,2-b]

Formula: C₉H₉NO₂S

Purity: Min. 95%

Molecular weight: 195.24 g/mol

Ref: 3D-DUA23903