CAS 58952-14-0

3,4-Dimethoxythiobenzamide

Description:

3,4-Dimethoxythiobenzamide is an organic compound characterized by the presence of a thiobenzamide functional group, which consists of a benzene ring substituted with two methoxy groups at the 3 and 4 positions, and a thiocarbonyl group. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents, reflecting its hydrophobic nature due to the aromatic structure. The methoxy groups enhance its electron-donating properties, potentially influencing its reactivity and interactions with biological systems. 3,4-Dimethoxythiobenzamide may exhibit various biological activities, making it of interest in pharmaceutical research. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of new therapeutic agents. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if ingested or inhaled. Proper storage conditions are also essential to maintain its stability and integrity.

Formula: C₉H₁₁NO₂S

InChI: InChI=1/C9H11NO2S/c1-11-7-4-3-6(9(10)13)5-8(7)12-2/h3-5H,1-2H3,(H2,10,13)

SMILES: COc1ccc(cc1OC)C(=N)S

Synonyms:

• 3,4-Dimethoxybenzenecarbothioamide
• Benzenecarbothioamide, 3,4-dimethoxy-

3,4-dimethoxybenzene-1-carbothioamide

CAS: 58952-14-0

Formula: C₉H₁₁NO₂S

Molecular weight: 197.2541

Ref: IN-DA00EB9P

3,4-Dimethoxythiobenzamide

CAS: 58952-14-0

Formula: C₉H₁₁NO₂S

Purity: 98.0%

Color and Shape: Solid

Molecular weight: 197.25

Ref: 10-F021337

3,4-dimethoxythiobenzamide

CAS: 58952-14-0

3,4-dimethoxythiobenzamide is a thiazole that has been shown to have potential antitumor effects. 3,4-dimethoxythiobenzamide inhibits the tyrosine kinase activity of platelets, which may contribute to its anti-cancer properties. It has also been shown to inhibit growth in colon cancer cells. 3,4-dimethoxythiobenzamide has been radiolabeled with positron and used as a radiotracer for positron emission tomography (PET) imaging of cancer cells. The drug binds to the cysteine sulfhydryl group on phosphotyrosine residues in proteins and forms covalent bonds with disulfide bonds, making it an excellent binding agent for proteins.

Formula: C₉H₁₁NO₂S

Purity: Min. 95%

Molecular weight: 197.25 g/mol

Ref: 3D-ICA95214