CAS 6265-92-5
:2-(4-Méthoxyphényl)benzothiazole
- 2-(4-Methoxy-phenyl)-benzothiazole
- 2-(4-Methoxyphenyl)Benzothiazole
- 2-(4-Methoxyphenyl)benzo[d]thiazole
- 2-(p-Methoxyphenyl)benzothiazole
- Benzothiazole, 2-(4-methoxyphenyl)-
- Benzothiazole, 2-(p-methoxyphenyl)-
- NSC 33161
2-(4-Methoxyphenyl)benzothiazole
CAS :Formule :C14H11NOSDegré de pureté :>98.0%(GC)Couleur et forme :Light yellow to Yellow to Green powder to crystalMasse moléculaire :241.312-(4-methoxyphenyl)benzo[d]thiazole
CAS :Formule :C14H11NOSDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :241.30822-(4-Methoxyphenyl)benzothiazole
CAS :2-(4-Methoxyphenyl)benzothiazoleDegré de pureté :98%Masse moléculaire :241.32g/mol2-(4-Methoxyphenyl)benzothiazole
CAS :2-(4-Methoxyphenyl)benzothiazole is a hydrogen-bond acceptor that is activated in the presence of an electron-withdrawing group. It has been shown to have anti-fungal properties and inhibitory properties against bacteria. 2-(4-Methoxyphenyl)benzothiazole also inhibits the activity of topoisomerase, which is an enzyme that controls DNA supercoiling and uncoiling, as well as DNA replication. The mechanism of this inhibition is not known, but it is thought to be due to the ability of 2-(4-methoxyphenyl)benzothiazole to form hydrogen bonds with the active site cysteine residues on topoisomerase I. 2-(4-Methoxyphenyl)benzothiazole also has been shown to be photophysical in nature, absorbing light at wavelengths of 350 nm and 480 nm and emitting light
Formule :C14H11NOSDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :241.31 g/mol




