4-Thiazoleethanethioic acid, α-[(triphenylmethoxy)imino]-2-[(triphenylmethyl)amino]-, S-2-benzothiazolyl ester, with CAS number 89605-32-3, is a complex organic compound characterized by its thiazole and benzothiazole moieties, which contribute to its potential biological activity. The presence of triphenyl groups suggests significant steric hindrance, which may influence its reactivity and solubility properties. This compound likely exhibits properties typical of thiazole derivatives, such as antimicrobial or antifungal activity, due to the sulfur and nitrogen atoms in its structure. The imino and thioester functionalities may also play a role in its reactivity, potentially allowing for nucleophilic attack or other chemical transformations. Additionally, the compound's stereochemistry, indicated by the (Z) configuration, may affect its interaction with biological targets. Overall, this substance is of interest in medicinal chemistry and may have applications in drug development or as a research tool in studying thiazole-related biological processes.

4-Thiazoleethanethioic acid,a-[(triphenylmethoxy)imino]-2-[(triphenylmethyl)amino]-,S-2-benzothiazolyl ester, (Z)-

89605-32-3: 4-Thiazoleethanethioic acid, α-[(triphenylmethoxy)imino]-2-[(triphenylmethyl)amino]-, S-2-benzothiazolyl ester, with CAS number 89605-32-3, is a complex organic compound characterized by its thiazole and benzothiazole moieties, which contribute to its potential biological activity. The presence of triphenyl groups suggests significant steric hindrance, which may influence its reactivity and solubility properties. This compound likely exhibits properties typical of thiazole derivatives, such as antimicrobial or antifungal activity, due to the sulfur and nitrogen atoms in its structure. The imino and thioester functionalities may also play a role in its reactivity, potentially allowing for nucleophilic attack or other chemical transformations. Additionally, the compound's stereochemistry, indicated by the (Z) configuration, may affect its interaction with biological targets. Overall, this substance is of interest in medicinal chemistry and may have applications in drug development or as a research tool in studying thiazole-related biological processes.

CAS 89605-32-3

4-Thiazoleethanethioic acid,a-[(triphenylmethoxy)imino]-2-[(triphenylmethyl)amino]-,S-2-benzothiazolyl ester, (Z)-

(Z)-α-[(Triphenylmethoxy)imino]-2-[(triphenylmethyl)amino]-4-thiazoleethanethioic Acid S-2-Benzothiazolyl Ester-13C,15N2

Ref: TR-T809027