Biosynth

The chemical substance known as (2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole, with the CAS number 2814-60-0, is a complex organic compound characterized by its unique structural features. It contains multiple functional groups, including hydrazone and benzothiazole moieties, which contribute to its potential biological activity. The presence of ethyl groups suggests a degree of hydrophobicity, which may influence its solubility and interaction with biological systems. The compound's structure indicates it may exhibit tautomerism due to the presence of the hydrazone linkage, allowing for different resonance forms. Additionally, the benzothiazole rings are known for their applications in pharmaceuticals and agrochemicals, often exhibiting antimicrobial and anti-inflammatory properties. The stereochemistry indicated by the (2Z) and (2E) designations suggests specific geometric configurations that can affect the compound's reactivity and biological interactions. Overall, this compound's intricate structure and functional groups make it a subject of interest in medicinal chemistry and material science.

(2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole

2814-60-0: The chemical substance known as (2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole, with the CAS number 2814-60-0, is a complex organic compound characterized by its unique structural features. It contains multiple functional groups, including hydrazone and benzothiazole moieties, which contribute to its potential biological activity. The presence of ethyl groups suggests a degree of hydrophobicity, which may influence its solubility and interaction with biological systems. The compound's structure indicates it may exhibit tautomerism due to the presence of the hydrazone linkage, allowing for different resonance forms. Additionally, the benzothiazole rings are known for their applications in pharmaceuticals and agrochemicals, often exhibiting antimicrobial and anti-inflammatory properties. The stereochemistry indicated by the (2Z) and (2E) designations suggests specific geometric configurations that can affect the compound's reactivity and biological interactions. Overall, this compound's intricate structure and functional groups make it a subject of interest in medicinal chemistry and material science.

<p>3,3'-Diethyl-2,2'-azinodibenzothiazole is an electron-rich molecule that can be used as a radical scavenger. It has been found to act as a quaternary ammonium salt and has been used in the synthesis of ethyl derivatives. 3,3'-Diethyl-2,2'-azinodibenzothiazole has been analyzed by electron spectroscopy and found to have a cation radical with unpaired electrons. This molecule is also capable of generating an anion radical when it interacts with oxygen or nitrogen gas. The density of 3,3'-diethyl-2,2'-azinodibenzothiazole is 1.8g/cm^3 at room temperature.</p>

CAS 2814-60-0

(2Z)-3-ethyl-2-[(2E)-(3-ethyl-1,3-benzothiazol-2(3H)-ylidene)hydrazono]-2,3-dihydro-1,3-benzothiazole

3,3'-Diethyl-2,2'-azinodibenzothiazole

Ref: 3D-FD174896