7382-41-4

Usage

Uses

Used in Pharmaceutical Industry:
2-(4-CHLOROPHENYL)-1-HYDRAZINECARBOTHIOAMIDE is used as a chemical intermediate for the synthesis of bioactive compounds, leveraging its thioamide functional group to contribute to the development of new pharmaceuticals.
Used in Agricultural Chemicals:
In the agricultural sector, 2-(4-CHLOROPHENYL)-1-HYDRAZINECARBOTHIOAMIDE is used as a building block in the formulation of agricultural chemicals, potentially enhancing crop protection and yield through its incorporation into effective compounds.
Used in Organic Synthesis:
2-(4-CHLOROPHENYL)-1-HYDRAZINECARBOTHIOAMIDE is utilized as a versatile intermediate in organic synthesis, allowing for the creation of a wide range of chemical products across various industries.

InChI:InChI=1/C7H8ClN3S/c8-5-1-3-6(4-2-5)10-11-7(9)12/h1-4,10H,(H3,9,11,12)

Upstream product

• 1147550-11-5 ammonium thiocyanate 
• 1073-69-4 N-4-chlorophenylhydrazine 
• 75-15-0 carbon disulfide 
• 106-47-8 4-chloro-aniline 
• 33608-73-0 (Z)-(4-chloro-phenyl)-diazenecarbonitrile 

Downstream Products

• 47154-67-6 2-[N'-(4-chloro-phenyl)-hydrazino]-5-phenyl-thiazol-4-ylamine 
• 65078-26-4 thiazolidin-2-one (4-chloro-phenyl)-hydrazone 
• 128997-69-3 1-(4-Chloro-phenyl)-5-pyridin-4-yl-1,2-dihydro-[1,2,4]triazole-3-thione 
• 99793-92-7 1-(4-Chloro-phenyl)-5-thiophen-2-yl-1,2-dihydro-[1,2,4]triazole-3-thione 
• 99793-89-2 1-(4-Chloro-phenyl)-5-(4-fluoro-phenyl)-1,2-dihydro-[1,2,4]triazole-3-thione 
• 99793-91-6 1-(4-Chloro-phenyl)-5-(2-chloro-phenyl)-1,2-dihydro-[1,2,4]triazole-3-thione 
• 99794-17-9 1-(4-Chloro-phenyl)-5-(2-methylsulfanyl-phenyl)-1,2-dihydro-[1,2,4]triazole-3-thione 
• 1254037-61-0 C₁₅H₁₂ClN₃O₂S₂ 
• 1254037-64-3 C₁₈H₁₉ClN₄O₂S₂ 
• 1254037-67-6 C₁₉H₂₁ClN₄O₂S₂ 
• 1220213-46-6 4-(1-(4-chlorophenyl)-3-(methylthio)-1H-1,2,4-triazol-5-yl)benzenesulfonamide 
• 1220213-29-5 1-(4-chlorophenyl)-3-(methylsulfinyl)-5-(4-(methylsulfonyl)phenyl)-1H-1,2,4-triazole 
• 1254037-70-1 C₁₉H₂₁ClN₄O₄S₂ 
• 1220213-52-4 4-(1-(4-chlorophenyl)-3-(methylsulfonyl)-1H-1,2,4-triazol-5-yl)benzenesulfonamide 

Relevant academic research and scientific papers

Synthesis, structure, spectroscopic studies (FT-IR, FT-Raman and UV), normal coordinate, NBO and NLO analysis of salicylaldehyde p-chlorophenylthiosemicarbazone

The thiosemicarbazone compound, salicylaldehyde p-chlorophenylthiosemicarbazone (abbreviated as SCPTSC) was synthesized by refluxing equimolar amounts of 4-(4-methyl phenyl)-3-thiosemicarbazide and salicylaldehyde in presence of one drop of conc. H2

Structure-activity studies of 4-phenyl-substituted 2′-benzoylpyridine thiosemicarbazones with potent and selective anti-tumour activity

2′-Benzoylpyridine thiosemicarbazones (BpT) are effective iron chelators and display potent anti-proliferative activity against tumour cells. In order to gain greater insight into the structure-activity relationships of the BpT chelators, ten new analogue

Anthelmintic 2 arylhydrazino and 2 arylazo 2 thiazolines

Some 2 arylhydrazino and 2 arylazo 2 thiazolines were synthesized for anthelmintic testing. The most potent compound, 2 (o tolylazo) 2 thiazoline, was orally effective in sheep against a broad range of helminths.