2-(4-Hydroxyphenyl)benzothiazole, with the CAS number 6265-55-0, is an organic compound characterized by its benzothiazole structure, which consists of a benzene ring fused to a thiazole ring. This compound features a hydroxyl group (-OH) attached to a phenyl group, enhancing its potential for hydrogen bonding and increasing its solubility in polar solvents. It typically appears as a solid at room temperature and may exhibit a range of colors depending on its purity and specific formulation. The compound is known for its applications in various fields, including as a fluorescent dye, in rubber manufacturing as an anti-oxidant, and in the development of materials with specific optical properties. Its chemical properties include moderate stability under standard conditions, but it may undergo degradation when exposed to strong acids or bases. Additionally, it may exhibit biological activity, making it of interest in pharmaceutical research. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

2-(4-Hydroxyphenyl)benzothiazole

6265-55-0: 2-(4-Hydroxyphenyl)-1,3-benzothiazole, 2-(4-Hydroxyphenyl)benzothiazole, 2-(p-Hydroxyphenyl)benzothiazole, 4-(1,3-Benzothiazol-2-Yl)Phenol, 4-(2-Benzothiazolyl)phenol, 4-(Benzo[d]thiazol-2-yl)phenol, 4-(Benzothiazol-2-yl)phenol, NSC 33004, Phenol, 4-(2-Benzothiazolyl)-, Phenol, p-2-benzothiazolyl-

4-(BENZO[D]THIAZOL-2-YL)PHENOL

4-(1,3-BENZOTHIAZOL-2-YL)PHENOL

4-(1,3-Benzothiazol-2-yl)phenol is an antibacterial agent that contains a methoxy group. It has been shown to have potent cytotoxicity against cancer cells and may be used for the treatment of cancer. 4-(1,3-Benzothiazol-2-yl)phenol is an oxidant that is able to form covalent bonds with proteins and other molecules through hydrogen bonding. The oxidation products of 4-(1,3-Benzothiazol-2-yl)phenol are also potent cytotoxins and inhibitors of bacterial growth. The molecular modeling studies on this compound indicate that it binds to DNA by intermolecular hydrogen bonding. This drug targets the enzyme thymidylate synthase, which catalyzes the conversion of dUMP to dTMP in the de novo pathway of DNA synthesis. 4-(1,3-Benzothiazol-2-yl)phenol has been

CAS 6265-55-0: 2-(4-Hydroxyphenyl)benzothiazole

4-(BENZO[D]THIAZOL-2-YL)PHENOL

Ref: 10-F302884

4-(1,3-BENZOTHIAZOL-2-YL)PHENOL

Ref: IN-DA00E8OT

4-(1,3-Benzothiazol-2-yl)phenol

Ref: 3D-GAA26555