96938-54-4

Basic information

• Product Name: N-benzoyl-N′-(2,4,6-trichlorophenyl)-thiourea
• Synonyms: N-benzoyl-N′-(2,4,6-trichlorophenyl)-thiourea
• CAS NO: 96938-54-4
• Molecular Weight: 359.663
• Mol File: 96938-54-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N-benzoyl-N′-(2,4,6-trichlorophenyl)-thiourea(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzoyl-N′-(2,4,6-trichlorophenyl)-thiourea(96938-54-4)
• EPA Substance Registry System: N-benzoyl-N′-(2,4,6-trichlorophenyl)-thiourea(96938-54-4)

Safety Data

• Hazardous Substances Data: 96938-54-4(Hazardous Substances Data)

Upstream product

• 532-55-8 Benzoyl isothiocyanate 
• 634-93-5 2,4,6-trichloroaniline 
• 540-72-7 sodium thiocyanide 
• 98-88-4 benzoyl chloride 
• 65-85-0 benzoic acid 

Downstream Products

• 16628-64-1 2-benzoylamino-4,6-dichloro-benzothiazole 
• 6590-95-0 2,6-dichlorophenylisothiocyanate 

Relevant articles and documents

Dual Roles of N,N-Dimethylformamide in Benzothiazoles Synthesis from N-Benzoyl-N′-(2,4,6-trichlorophenyl)thiourea

Abstract: N,N-Dimethylformamide (DMF) is not only a common polar solvent in chemistry, but also a reaction reagent, a catalyst and a stabilizer. In this paper, a new reaction was found accidently where DMF acted as both solvent and catalyst. By dissolving

Application of N-substituted aryl (arylformamido)-N'-substituted arylformyl thiourea compound in inhibition of blue alga growth

The invention relates to an application of an N-substituted aryl (arylformamido)-N'-substituted arylformyl thiourea compound in inhibition of blue alga growth. The N-substituted aryl-N'-substituted arylformyl thiourea compound with a general formula I and

Solution-phase microwave assisted parallel synthesis of N,N′-disubstituted thioureas derived from benzoic acid: Biological evaluation and molecular docking studies

An efficient and facile microwave-assisted solution phase parallel synthesis for a 26-member library of N,N′-disubstituted thiourea analogs were accomplished successfully. The reaction time for synthesis of analogs was drastically reduced from a reported 8-12 h to only 10 min. Compounds were more than 95% pure, as characterized by modern analytical techniques, i.e. 1H & 13C NMR and FT-IR. The solid phase structural analysis has also been performed by single crystal XRD analysis. Synthesized compounds were preliminary screened for their in vitro urease inhibition and antifungal activity. Most of the compounds were found to be potent inhibitors of urease. However, the most significant activity was found for 11 with IC 50 of 1.67 μM. The docking scores correlate with the IC 50 values of inhibitors.