CAS 64165-98-6

3,5-Hexadiyne-1,2-diol,6-[5-(1-propyn-1-yl)-2-thienyl]-

Description:

3,5-Hexadiyne-1,2-diol,6-[5-(1-propyn-1-yl)-2-thienyl]- is a complex organic compound characterized by its unique structure, which includes a hexadiyne backbone and functional groups such as diol and thienyl moieties. This compound features multiple triple bonds, contributing to its reactivity and potential applications in organic synthesis and materials science. The presence of hydroxyl (-OH) groups indicates that it can engage in hydrogen bonding, which may influence its solubility and interaction with other substances. The thienyl group, derived from thiophene, introduces aromatic characteristics, enhancing the compound's stability and electronic properties. This compound may exhibit interesting optical and electronic behaviors, making it a candidate for research in fields such as organic electronics or photonics. Additionally, its structural complexity suggests potential utility in medicinal chemistry or as a building block for more intricate molecular architectures. However, specific safety and handling guidelines should be followed due to the presence of reactive functional groups.

Formula: C₁₃H₁₀O₂S

Synonyms:

• 3,5-Hexadiyne-1,2-diol,6-[5-(1-propynyl)-2-thienyl]- (9CI)
• Echinoynethiophene A
• Thiophene A diol
• ThiopheneE

Echinoynethiophene A

CAS: 64165-98-6

Echinoynethiophene A is a natural product from Laggera pterodonta

Formula: C₁₃H₁₀O₂S

Purity: 98%

Color and Shape: Solid

Molecular weight: 230.28

Ref: TM-TN2381

Echinoynethiophene A

CAS: 64165-98-6

Formula: C₁₃H₁₀O₂S

Purity: 95%~99%

Molecular weight: 230.281

Ref: BP-SBP00399

Echinoynethiophene A

CAS: 64165-98-6

Echinoynethiophene A is an antibacterial compound that inhibits bacterial growth by binding to the bromodomain of transiliensis. It has been shown to inhibit mosquito larvae development in ethanol extract and inhibit the growth of bacteria in a laboratory setting. This compound has shown antibacterial activity against Gram-positive bacteria, such as Bacillus cereus and Staphylococcus aureus, and Gram-negative bacteria, such as Escherichia coli and Salmonella enterica serovar Typhi. Echinoynethiophene A also shows anti-inflammatory properties, which may be due to its ability to inhibit fatty acid synthesis. The natural compound has been identified in Chinese medicinal herbs from the genus Saussurea L.

Formula: C₁₃H₁₀O₂S

Purity: Min. 95%

Molecular weight: 230.28 g/mol

Ref: 3D-PCA16598