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

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

Uses

Used in Agricultural Industry:
Chlorobenzuron is used as an insect growth regulator for controlling a broad spectrum of agricultural pests. It is particularly effective against certain species of moths, beetles, and flies, which are known to cause significant damage to crops. By preventing these pests from completing their life cycle, Chlorobenzuron helps protect crops such as cotton, corn, and vegetables from the detrimental effects of infestations.
It is crucial to adhere to regulatory guidelines and safety precautions when using Chlorobenzuron to ensure minimal negative impacts on non-target organisms and the environment. This responsible use ensures the sustainability of agricultural practices and the preservation of ecological balance.

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.

NEW SYNTHESIS OF N-ACYLUREA DERIVATIVES

S-Allyl N-acylmonothiocarbamates react in boiling benzene with primary and secondary amines in the presence of catalytic amounts of triethylamine.In this reaction, the S-allyl group is replaced with the amino group under formation of N-acylurea derivatives in 45-90percent yields.The wide applicability of the reaction is demonstrated by the synthesis of eighty four N-acyl-N'-substituted and N-acyl-N',N'-disubstituted ureas with various aliphatic, aromatic and heterocyclic substituents.

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.