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Atomfair 2-(2-Hydroxyphenyl)benzothiazole C13H9NOS
Description 2-(2-Hydroxyphenyl)benzothiazole (CAS No. 104197-13-9), also known as 2-(1,3-benzothiazol-2-yl)phenol , is a high-purity organic compound with the molecular formula C13H9NOS . This benzothiazole derivative features a hydroxyphenyl substituent, making it a versatile intermediate for synthetic chemistry and material science applications. Its molecular weight of 227.28 g/mol and distinct structural properties lend it utility in coordination chemistry, fluorescence studies, and as a ligand for metal complexes. The compound is supplied as a crystalline solid with ??98% purity (HPLC), ensuring consistency for research and industrial use. Store in a cool, dry place, protected from light to maintain stability.
Description
Description
2-(2-Hydroxyphenyl)benzothiazole (CAS No. 104197-13-9), also known as 2-(1,3-benzothiazol-2-yl)phenol, is a high-purity organic compound with the molecular formula C13H9NOS. This benzothiazole derivative features a hydroxyphenyl substituent, making it a versatile intermediate for synthetic chemistry and material science applications. Its molecular weight of 227.28 g/mol and distinct structural properties lend it utility in coordination chemistry, fluorescence studies, and as a ligand for metal complexes. The compound is supplied as a crystalline solid with ??98% purity (HPLC), ensuring consistency for research and industrial use. Store in a cool, dry place, protected from light to maintain stability.
- CAS No: 104197-13-9
- Molecular Formula: C13H9NOS
- Molecular Weight: 227.28
- Exact Mass: 227.04048508
- Monoisotopic Mass: 227.04048508
- IUPAC Name: 2-(1,3-benzothiazol-2-yl)phenol
- SMILES: C1=CC=C(C(=C1)C2=NC3=CC=CC=C3S2)O
- Synonyms: 2-(2-Hydroxyphenyl)benzothiazole, 3411-95-8, 2-(1,3-Benzothiazol-2-yl)phenol, Phenol, 2-(2-benzothiazolyl)-, 2-(o-Hydroxyphenyl)benzothiazole
Application
2-(2-Hydroxyphenyl)benzothiazole is widely used as a chelating agent in the synthesis of luminescent metal complexes for optoelectronic devices. Its fluorescence properties make it valuable in sensor development and bioimaging probes. Researchers also employ it as a building block for organic semiconductors and photostabilizers due to its conjugated benzothiazole-phenol system.
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