57160-47-1

Basic information

• Product Name: CHLOROBENZURON
• Synonyms: 2-Chloro-N-(((4-chlorophenyl)amino)carbonyl)benzamide;Benzamide, 2-chloro-N-(((4-chlorophenyl)amino)carbonyl)-;2,6-dichloro-N-[(4-chlorophenyl)carbamoyl]benzamide;Chlorbenzuron solution;Chlorobenzuron, 10 μg /μL in acetonitrile;2-chloro-N-((4-chlorophenyl)carbamoyl)benzamide;Chlorobenzuron Solution, 1000ppm
• CAS NO: 57160-47-1
• Molecular Formula: C₁₄H₁₀Cl₂N₂O₂
• Molecular Weight: 309.151
• EINECS: 200-589-5
• Mol File: 57160-47-1.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Density: 1.44g/cm³
• Refractive Index: 1.656
• PKA: 9.84±0.46(Predicted)
• CAS DataBase Reference: CHLOROBENZURON(CAS DataBase Reference)
• NIST Chemistry Reference: CHLOROBENZURON(57160-47-1)
• EPA Substance Registry System: CHLOROBENZURON(57160-47-1)

Safety Data

• Hazardous Substances Data: 57160-47-1(Hazardous Substances Data)

Usage

General Description

Chlorobenzuron is a chemical compound belonging to the class of benzoylphenylureas, which is commonly used as an insect growth regulator in controlling agricultural pests. It acts by interfering with the development of insect larvae, preventing them from molting and ultimately causing their death. Chlorobenzuron is effective against a wide range of insect pests, including certain species of moths, beetles, and flies. It is used in various crops such as cotton, corn, and vegetables to protect them from damage caused by these pests. However, it is important to use chlorobenzuron in accordance with regulatory guidelines and safety precautions to minimize any potential negative impacts on non-target organisms and the environment.

InChI:InChI=1/C14H10Cl2N2O2/c15-9-5-7-10(8-6-9)17-14(20)18-13(19)11-3-1-2-4-12(11)16/h1-8H,(H2,17,18,19,20)

Upstream product

• 104-12-1 p-chlorphenylisocyanate 
• 89-97-4 2-CHLOROBENZYLAMINE 
• 113283-17-3 S-(2-propenyl) N-(2-chlorobenzoyl)monothiocarbamate 
• 106-47-8 4-chloro-aniline 
• 609-66-5 2-chlorobenzamide 

Downstream Products

• 610-96-8 methyl chlorobenzoate 
• 140-38-5 N-(4-chlorophenyl)urea 

Relevant articles and documents

Hydrogen bond directed aerobic oxidation of amines via photoredox catalysis

An application of H-bonding interactions for directing the α-C-H oxidation of amines to amides and amino-ketones catalyzed by an organic photocatalyst is reported. The high efficiency of this method is demonstrated by the aerobic oxidation of pyrrolidines, diarylamines and benzylamines bearing urea groups with high yields and a wide substrate scope.

KINETICS OF METHANOLYSIS OF 1-(2-HALOGENO AND 2,6-DIHALOGENOBENZOYL)-3-(4-CHLOROPHENYL)UREAS

The methanolysis kinetics has been measured of 1-(2,6-difluorobenzoyl)-3-(4-chlorophenyl)urea (a larvicidal insecticide Dimilin) and of four other mono- and dihalogenobenzoyl derivatives.Polar and steric effects of halogen on the rate and dissociation constants is discussed.