2-Fluorobenzenecarbothioamide, with the CAS number 75907-82-3, is an organic compound characterized by the presence of a fluorine atom attached to a benzene ring, along with a carbothioamide functional group. This compound features a thiocarbonyl group (C=S) linked to an amine (NH2), which contributes to its reactivity and potential applications in various chemical reactions. The fluorine substituent can influence the electronic properties of the molecule, potentially enhancing its reactivity or altering its interaction with biological systems. Typically, compounds like 2-fluorobenzenecarbothioamide may exhibit moderate solubility in polar solvents due to the presence of the amide group, while the aromatic ring can provide stability and hydrophobic characteristics. This compound may be of interest in medicinal chemistry and materials science, where its unique properties can be exploited for the development of pharmaceuticals or agrochemicals. As with many thiocarbonyl compounds, it may also participate in nucleophilic addition reactions, making it a versatile building block in organic synthesis.

2-fluorobenzenecarbothioamide

75907-82-3: 2-Fluorobenzenecarbothioamide, with the CAS number 75907-82-3, is an organic compound characterized by the presence of a fluorine atom attached to a benzene ring, along with a carbothioamide functional group. This compound features a thiocarbonyl group (C=S) linked to an amine (NH2), which contributes to its reactivity and potential applications in various chemical reactions. The fluorine substituent can influence the electronic properties of the molecule, potentially enhancing its reactivity or altering its interaction with biological systems. Typically, compounds like 2-fluorobenzenecarbothioamide may exhibit moderate solubility in polar solvents due to the presence of the amide group, while the aromatic ring can provide stability and hydrophobic characteristics. This compound may be of interest in medicinal chemistry and materials science, where its unique properties can be exploited for the development of pharmaceuticals or agrochemicals. As with many thiocarbonyl compounds, it may also participate in nucleophilic addition reactions, making it a versatile building block in organic synthesis.

CAS 75907-82-3

2-fluorobenzenecarbothioamide

2-Fluorobenzothioamide

Ref: IN-DA005TC6

2-Fluorothiobenzamide

Ref: 54-PC8237

2-Fluorothiobenzamide

Ref: 10-F021323