2,3-Dichlorothiobenzamide is an organic compound characterized by the presence of a thiobenzamide functional group, which consists of a benzene ring substituted with two chlorine atoms at the 2 and 3 positions and a thiocarbonyl group (–C(=S)–NH2). This compound typically appears as a solid and is known for its potential applications in various fields, including pharmaceuticals and agrochemicals. Its molecular structure contributes to its reactivity, particularly in nucleophilic substitution reactions due to the presence of the thiocarbonyl group. The chlorine substituents can influence the compound's electronic properties and steric hindrance, affecting its biological activity and interaction with other molecules. Additionally, 2,3-Dichlorothiobenzamide may exhibit specific solubility characteristics, often being soluble in organic solvents while having limited solubility in water. Safety data should be consulted for handling and storage, as halogenated compounds can pose health risks. Overall, this compound's unique structure and properties make it of interest in synthetic chemistry and material science.

2,3-Dichlorothiobenzamide

84863-83-2: 2,3-Dichlorothiobenzamide is an organic compound characterized by the presence of a thiobenzamide functional group, which consists of a benzene ring substituted with two chlorine atoms at the 2 and 3 positions and a thiocarbonyl group (–C(=S)–NH2). This compound typically appears as a solid and is known for its potential applications in various fields, including pharmaceuticals and agrochemicals. Its molecular structure contributes to its reactivity, particularly in nucleophilic substitution reactions due to the presence of the thiocarbonyl group. The chlorine substituents can influence the compound's electronic properties and steric hindrance, affecting its biological activity and interaction with other molecules. Additionally, 2,3-Dichlorothiobenzamide may exhibit specific solubility characteristics, often being soluble in organic solvents while having limited solubility in water. Safety data should be consulted for handling and storage, as halogenated compounds can pose health risks. Overall, this compound's unique structure and properties make it of interest in synthetic chemistry and material science.

2,3-dichlorobenzene-1-carbothioamide

<p>2,3-dichlorobenzene-1-carbothioamide</p>

CAS 84863-83-2

2,3-Dichlorothiobenzamide

2,3-dichlorobenzene-1-carbothioamide

Ref: IN-DA003FHV

2,3-dichlorobenzene-1-carbothioamide

Ref: 54-OR29605

2,3-Dichlorothiobenzamide

Ref: 10-F021321