CAS 6265-92-5
:2-(4-Methoxyphenyl)benzothiazole
Description:
2-(4-Methoxyphenyl)benzothiazole, with the CAS number 6265-92-5, is an organic compound characterized by its benzothiazole core, which is a bicyclic structure containing both a benzene ring and a thiazole ring. This compound features a methoxy group (-OCH3) attached to a phenyl ring, which is further connected to the benzothiazole moiety. The presence of the methoxy group enhances its solubility and can influence its electronic properties, making it potentially useful in various applications, including pharmaceuticals and materials science. The compound may exhibit fluorescence, which is a characteristic of many benzothiazole derivatives, and it could be involved in biological activities, such as antimicrobial or anticancer properties. Its molecular structure allows for interactions with biological targets, making it of interest in medicinal chemistry. Additionally, the compound's stability and reactivity can be influenced by the substituents on the aromatic rings, which can affect its behavior in chemical reactions and its potential applications in different fields.
Formula:C14H11NOS
InChI:InChI=1S/C14H11NOS/c1-16-11-8-6-10(7-9-11)14-15-12-4-2-3-5-13(12)17-14/h2-9H,1H3
InChI key:InChIKey=AOPZIJQISHFZBN-UHFFFAOYSA-N
SMILES:O(C)C1=CC=C(C2=NC=3C(S2)=CC=CC3)C=C1
Synonyms:- 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
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Found 5 products.
2-(4-Methoxyphenyl)benzothiazole
CAS:Formula:C14H11NOSPurity:>98.0%(GC)Color and Shape:Light yellow to Yellow to Green powder to crystalMolecular weight:241.312-(4-methoxyphenyl)benzo[d]thiazole
CAS:Formula:C14H11NOSPurity:98%Color and Shape:SolidMolecular weight:241.30822-(4-Methoxyphenyl)benzothiazole
CAS:2-(4-Methoxyphenyl)benzothiazolePurity:98%Molecular weight:241.32g/mol2-(4-Methoxyphenyl)benzothiazole
CAS:<p>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</p>Formula:C14H11NOSPurity:Min. 95%Color and Shape:PowderMolecular weight:241.31 g/mol





