2,4-Dimethylbenzenecarbothioamide, with the CAS number 57182-70-4, is an organic compound characterized by the presence of a thiocarbonyl group (-C(=S)NHR) attached to a dimethyl-substituted benzene ring. This compound features a benzene ring with two methyl groups located at the 2 and 4 positions, which influences its physical and chemical properties, such as solubility and reactivity. The thiocarbonyl functional group imparts unique characteristics, including potential reactivity in nucleophilic addition reactions and the ability to form thiourea derivatives. The presence of the methyl groups can enhance the compound's lipophilicity, affecting its interaction with biological systems. Additionally, 2,4-dimethylbenzenecarbothioamide may exhibit specific spectral properties, making it identifiable through techniques like NMR and IR spectroscopy. Its applications could range from synthetic intermediates in organic chemistry to potential roles in pharmaceuticals or agrochemicals, depending on its reactivity and biological activity. As with many thiocarbonyl compounds, safety and handling precautions should be observed due to potential toxicity.

2,4-dimethylbenzenecarbothioamide

57182-70-4: 2,4-Dimethylbenzenecarbothioamide, with the CAS number 57182-70-4, is an organic compound characterized by the presence of a thiocarbonyl group (-C(=S)NHR) attached to a dimethyl-substituted benzene ring. This compound features a benzene ring with two methyl groups located at the 2 and 4 positions, which influences its physical and chemical properties, such as solubility and reactivity. The thiocarbonyl functional group imparts unique characteristics, including potential reactivity in nucleophilic addition reactions and the ability to form thiourea derivatives. The presence of the methyl groups can enhance the compound's lipophilicity, affecting its interaction with biological systems. Additionally, 2,4-dimethylbenzenecarbothioamide may exhibit specific spectral properties, making it identifiable through techniques like NMR and IR spectroscopy. Its applications could range from synthetic intermediates in organic chemistry to potential roles in pharmaceuticals or agrochemicals, depending on its reactivity and biological activity. As with many thiocarbonyl compounds, safety and handling precautions should be observed due to potential toxicity.

CAS 57182-70-4

2,4-dimethylbenzenecarbothioamide

2,4-Dimethylthiobenzamide

Ref: IN-DA00EV40

2,4-Dimethylbenzene-1-carbothioamide

Ref: 3D-HCA18270