782-94-5

Basic information

• Product Name: 2,2,2-TRIFLUOROETHYL 4-CHLOROPHENYLCARBAMATE
• Synonyms: 2,2,2-trifluoroethyl 4-chlorophenylcarbamate
• CAS NO: 782-94-5
• Molecular Formula: C₉H₇ClF₃NO₂
• Molecular Weight: 253.61
• Mol File: 782-94-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 227.916°C at 760 mmHg
• Flash Point: 91.641°C
• Appearance: /
• Density: 1.46g/cm³
• Vapor Pressure: 0.076mmHg at 25°C
• Refractive Index: 1.513
• CAS DataBase Reference: 2,2,2-TRIFLUOROETHYL 4-CHLOROPHENYLCARBAMATE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,2-TRIFLUOROETHYL 4-CHLOROPHENYLCARBAMATE(782-94-5)
• EPA Substance Registry System: 2,2,2-TRIFLUOROETHYL 4-CHLOROPHENYLCARBAMATE(782-94-5)

Safety Data

• Hazardous Substances Data: 782-94-5(Hazardous Substances Data)

Usage

Common uses

Pesticide and insecticide for controlling various pests, including insects, mites, and nematodes.

Mode of action

Disrupts the nervous system of pests, leading to paralysis and death.

Application methods

Foliar spray or soil treatment in agricultural and horticultural settings.

Safety concerns

Can be harmful to humans and non-target organisms if not used properly.

InChI:InChI=1/C9H7ClF3NO2/c10-6-1-3-7(4-2-6)14-8(15)16-5-9(11,12)13/h1-4H,5H2,(H,14,15)

Upstream product

• 75-89-8 2,2,2-trifluoroethanol 
• 104-12-1 p-chlorphenylisocyanate 
• 27746-99-2 2,2,2-trifluoroethyl chloroformate 
• 106-47-8 4-chloro-aniline 

Downstream Products

• 900657-45-6 1-(4-chlorophenyl)-3-(1-methylpiperidin-4-yl)urea 

Relevant articles and documents

A facile synthesis of unsymmetrical ureas

A facile and versatile method for the synthesis of unsymmetrical ureas from readily available reagents is reported. In the first step trifluoroethylchloroformate is reacted with a stoichiometric amount of a primary amine to give an intermediate trifluoroethyl carbamate. The addition of a second amine (primary or secondary) to the trifluoroethyl carbamate furnishes corresponding unsymmetrical ureas in 75-85% yield. A simple workup procedure, the high yields obtained, and the purity of the isolated products are suitable for the parallel synthesis of combinatorial libraries of unsymmetrical ureas with high structural and functional diversity.