CAS 135149-43-8

2-Thiophenecarboxylic acid, 5-formyl-, 1,1-dimethylethyl ester

Description:

2-Thiophenecarboxylic acid, 5-formyl-, 1,1-dimethylethyl ester, with the CAS number 135149-43-8, is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxylic acid functional group and an ester linkage, indicating it can participate in various chemical reactions typical of esters, such as hydrolysis and transesterification. The presence of the formyl group suggests that it can also undergo reactions typical of aldehydes, such as oxidation or condensation. The tert-butyl ester group enhances its lipophilicity, potentially influencing its solubility in organic solvents. This compound may exhibit biological activity, making it of interest in pharmaceutical and agrochemical research. Its unique structure allows for potential applications in synthesis and material science. As with many organic compounds, safety data should be consulted to understand its handling and toxicity.

Formula: C₁₀H₁₂O₃S

tert-Butyl 5-formylthiophene-2-carboxylate

CAS: 135149-43-8

tert-Butyl 5-formylthiophene-2-carboxylate is an acylguanidine that has been shown to have a high affinity for bone, mediating its effects on osteoporosis. This compound is selective for bone and inhibits the activity of steroid sulfatase, which is responsible for breaking down steroids in the body. It is also lipophilic and can penetrate into the cell membrane, where it binds to the receptor sites of cyclic AMP and blocks their activation by acetylcholine or other substances. This results in a decrease in calcium uptake into cells, reducing skeletal breakdown and enhancing bone formation. Structurally, tert-butyl 5-formylthiophene-2-carboxylate contains a thiophene ring that provides it with this selectivity.

Formula: C₁₀H₁₂O₃S

Purity: Min. 95%

Molecular weight: 212.27 g/mol

Ref: 3D-KFA14943