CAS 36341-25-0
:4-(1,3-benzothiazol-2-yl)-2-methoxyphenol
Description:
4-(1,3-benzothiazol-2-yl)-2-methoxyphenol, with the CAS number 36341-25-0, is an organic compound characterized by its complex structure that includes a benzothiazole moiety and a methoxyphenol group. This compound typically exhibits properties such as being a solid at room temperature, with potential applications in various fields, including pharmaceuticals and materials science. It may demonstrate biological activity, particularly in antimicrobial or antioxidant capacities, due to the presence of the phenolic group. The benzothiazole component can contribute to its stability and reactivity, making it a subject of interest in synthetic chemistry. Additionally, the compound's solubility and reactivity can vary based on the solvent and conditions used, which is crucial for its application in research and industry. Overall, 4-(1,3-benzothiazol-2-yl)-2-methoxyphenol represents a versatile chemical entity with potential utility in diverse chemical and biological contexts.
Formula:C14H11NO2S
InChI:InChI=1/C14H11NO2S/c1-17-12-8-9(6-7-11(12)16)14-15-10-4-2-3-5-13(10)18-14/h2-8,16H,1H3
SMILES:COc1cc(ccc1O)c1nc2ccccc2s1
Synonyms:- 4-Benzothiazol-2-yl-2-methoxy-phenol
- Phenol, 4-(2-Benzothiazolyl)-2-Methoxy-
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Found 5 products.
4-(1,3-Benzothiazol-2-yl)-2-methoxyphenol
CAS:Formula:C14H11NO2SPurity:98%Color and Shape:SolidMolecular weight:257.30764-(Benzo[D]Thiazol-2-Yl)-2-Methoxyphenol
CAS:4-(Benzo[D]Thiazol-2-Yl)-2-MethoxyphenolPurity:98%Molecular weight:257.31g/molYL-109
CAS:<p>YL-109, a novel anticancer agent, can inhibit breast Y cell growth and invasiveness in vitro and in vivo.</p>Formula:C14H11NO2SPurity:99.77% - ≥95%Color and Shape:SolidMolecular weight:257.31



