4-Chlorothieno[2,3-d]pyrimidine-6-carboxylic acid is a heterocyclic compound characterized by its unique bicyclic structure that incorporates both a thieno and pyrimidine ring. The presence of a chlorine atom at the 4-position of the thieno ring and a carboxylic acid functional group at the 6-position contributes to its chemical reactivity and potential biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid group. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of compounds targeting specific biological pathways. The compound's properties, such as melting point, boiling point, and spectral characteristics, can vary based on purity and environmental conditions. Additionally, its reactivity can be influenced by the presence of the chlorine substituent, which may participate in electrophilic aromatic substitution reactions. Overall, 4-chlorothieno[2,3-d]pyrimidine-6-carboxylic acid is of interest in medicinal chemistry and material science due to its structural features and potential functional applications.

4-chlorothieno[2,3-d]pyrimidine-6-carboxylic acid

86825-96-9: 4-Chlorothieno[2,3-d]pyrimidine-6-carboxylic acid is a heterocyclic compound characterized by its unique bicyclic structure that incorporates both a thieno and pyrimidine ring. The presence of a chlorine atom at the 4-position of the thieno ring and a carboxylic acid functional group at the 6-position contributes to its chemical reactivity and potential biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid group. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of compounds targeting specific biological pathways. The compound's properties, such as melting point, boiling point, and spectral characteristics, can vary based on purity and environmental conditions. Additionally, its reactivity can be influenced by the presence of the chlorine substituent, which may participate in electrophilic aromatic substitution reactions. Overall, 4-chlorothieno[2,3-d]pyrimidine-6-carboxylic acid is of interest in medicinal chemistry and material science due to its structural features and potential functional applications.

Thieno[2,3-d]pyrimidine-6-carboxylic acid, 4-chloro-

4-Chlorothieno[2,3-d]pyrimidine-6-carboxylic acid

CAS 86825-96-9

4-chlorothieno[2,3-d]pyrimidine-6-carboxylic acid

Thieno[2,3-d]pyrimidine-6-carboxylic acid, 4-chloro-

Ref: IN-DA00IE7X

4-Chlorothieno[2,3-d]pyrimidine-6-carboxylic acid

Ref: 54-OR313023

4-CHLOROTHIENO[2,3-D]PYRIMIDINE-6-CARBOXYLIC ACID

Ref: 10-F302080

4-Chlorothieno[2,3-d]pyrimidine-6-carboxylic acid

Ref: 3D-LDA82596