1960-88-9

Basic information

• Product Name: 1,3-Bis[4-(trifluoromethyl)phenyl]urea
• Synonyms: 1,3-Bis[4-(trifluoromethyl)phenyl]urea;N,N'-Bis[4-(trifluoromethyl)phenyl]urea
• CAS NO: 1960-88-9
• Molecular Formula: C₁₅H₁₀F₆N₂O
• Molecular Weight: 348.2431192
• Mol File: 1960-88-9.mol
• Article Data: 18

Chemical Properties

• Melting Point: 209-210 °C (decomp)
• Boiling Point: 287.1±40.0 °C(Predicted)
• Appearance: /
• Density: 1.470±0.06 g/cm3(Predicted)
• PKA: 13.13±0.70(Predicted)
• CAS DataBase Reference: 1,3-Bis[4-(trifluoromethyl)phenyl]urea(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Bis[4-(trifluoromethyl)phenyl]urea(1960-88-9)
• EPA Substance Registry System: 1,3-Bis[4-(trifluoromethyl)phenyl]urea(1960-88-9)

Safety Data

• Hazardous Substances Data: 1960-88-9(Hazardous Substances Data)

Usage

Description

1,3-Bis[4-(trifluoromethyl)phenyl]urea is a urea derivative with the molecular formula C15H10F6N2O. It is an organic compound that is primarily used as a pesticide in agriculture. This chemical features two trifluoromethylphenyl groups attached to a central urea moiety, resulting in a white crystalline solid at room temperature. It is sparingly soluble in water but more soluble in organic solvents.
Used in Agricultural Industry:
1,3-Bis[4-(trifluoromethyl)phenyl]urea is used as a pesticide for controlling sucking pests on a variety of agricultural crops. It functions by interfering with the insect's molting process, disrupting their growth and ultimately leading to their death. Careful handling and adherence to safety guidelines are essential when using this chemical.

Upstream product

• 455-14-1 4-trifluoromethylphenylamine 
• 1548-13-6 p-trifluoromethyl-phenylisocyanate 
• 530-62-1 1,1'-carbonyldiimidazole 
• 1645-65-4 4-(trifluoromethyl)phenyl isothiocyanate 
• 124-38-9 carbon dioxide 
• 98-16-8 3-trifluoromethylaniline 
• 74702-40-2 N-(4-(trifluoromethyl)phenyl)formamide 
• 3582-05-6 trifluoromethyl trifluoromethanesulfonate 
• 24424-99-5 di-tert-butyl dicarbonate 
• 74467-05-3 N-hydroxy-4-(trifluoromethyl)benzenecarboximidoyl chloride 

Relevant articles and documents

EFFECTS ON N,N'-BIS-(4-TRIFLUOROMETHYLPHENYL)-UREA ON ISOLATED PLANT MITOCHONDRIA AND THYLAKOID MEMBRANES

The N,N'-bis(trifluoromethylphenyl)-urea is demonstrated to be powerful uncoupler of ATP formation in plant mitochondria and thylakoid membranes.In mitochondria, the full uncoupling effect was obtained at a concentration of 3 μM uncoupling agent in the me

Amide-assisted rearrangement of hydroxyarylformimidoyl chloride to diarylurea

A novel amide-assisted rearrangement reaction of hydroxybenzimidoyl chloride has been established for the efficient synthesis of 1,3-diphenylurea derivatives. A variety of electronically and sterically different 1,3-diphenylurea derivatives can be obtained in good to excellent yields, and a proposed reaction mechanism is also presented.

Hydrosilane-Assisted Synthesis of Urea Derivatives from CO2and Amines

A methodology employing CO2, amines, and phenylsilane was discussed to access aryl- or alkyl-substituted urea derivatives. This procedure was characterized by adopting hydrosilane to promote the formation of ureas directly, without the need to prepare silylamines in advance. Control reactions suggested that FeCl3 was a favorable additive for the generation of ureas, and this 1,5,7-triazabicyclo[4.4.0]dec-5-ene-catalyzed reaction might proceed through nucleophilic addition, silicon migration, and the subsequent formal substitution of silylcarbamate.