2989-98-2

Basic information

• Product Name: 3-BROMOPHENYLUREA
• Synonyms: 3-BROMOPHENYLUREA;BUTTPARK 120\07-55;3-Bromophenylurea,97%;1-(3-Bromophenyl)urea;3-Ureido-1-bromobenzene
• CAS NO: 2989-98-2
• Molecular Formula: C₇H₇BrN₂O
• Molecular Weight: 215.05
• EINECS: -0
• Mol File: 2989-98-2.mol
• Article Data: 10

Chemical Properties

• Melting Point: 166-168°C
• Boiling Point: 289℃
• Flash Point: 128℃
• Appearance: /
• Density: 1.708
• Vapor Pressure: 0.00233mmHg at 25°C
• Refractive Index: 1.671
• Storage Temp.: 2-8°C
• BRN: 2718463
• CAS DataBase Reference: 3-BROMOPHENYLUREA(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMOPHENYLUREA(2989-98-2)
• EPA Substance Registry System: 3-BROMOPHENYLUREA(2989-98-2)

Safety Data

• Safety Statements: 22-24/25
• Hazardous Substances Data: 2989-98-2(Hazardous Substances Data)

Usage

General Description

3-Bromophenylurea is a chemical compound with the molecular formula C7H6BrN3O. It is a derivative of phenylurea, with a bromine atom attached to the phenyl ring. 3-BROMOPHENYLUREA is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It has been shown to exhibit herbicidal activity, making it useful in weed control products. 3-Bromophenylurea has also been studied for its potential as a corrosion inhibitor in industries such as oil and gas. Additionally, it has been investigated for its antifungal properties, and has shown promise as a potential antifungal agent. Overall, 3-Bromophenylurea is a versatile chemical with diverse applications in various industries.

InChI:InChI=1/C7H7BrN2O/c8-5-2-1-3-6(4-5)10-7(9)11/h1-4H,(H3,9,10,11)

Upstream product

• 591-19-5 m-Bromoaniline 
• 57-13-6 urea 
• 917-61-3 sodium isocyanate 
• 25203-27-4 ethyl 3-bromophenylcarbamate 
• 70590-12-4 N-(3-bromophenyl)cyanamide 
• 590-28-3 potassium cyanate 

Downstream Products

• 73469-89-3 N-(3-bromophenyl)hydrazine carboxamide 

Relevant articles and documents

Dual palladium-photoredox catalyzed chemoselective C-H arylation of phenylureas

A highly chemoselective C-H arylation of phenylureas has been accomplished using dual palladium-photoredox catalysis at room temperature without any additives, base or external oxidants. Regioselective C-H arylation ofN,N'-diaryl substituted unsymmetrical phenylureas has also been accomplished by a careful choice of aryl groups.

Superparamagnetic Fe3O4 Nanoparticles in a Deep Eutectic Solvent: An Efficient and Recyclable Catalytic System for the Synthesis of Primary Carbamates and Monosubstituted Ureas

Superparamagnetic Fe3O4 nanoparticles were used to synthesize various primary carbamates as well as monosubstituted and N,N-disubstituted ureas. This efficient phosgene-free process used urea as an eco-friendly carbonyl source in the presence of a biocompatible deep eutectic solvent (DES) to provide an inexpensive and attractive route that afforded the products in moderate to excellent yields. The employed DES serves both a catalytic role and as the green reaction medium. The magnetic nanocatalyst and DES can been reused several times without a significant loss of activity.

4-Dodecylbenzenesulfonic acid (DBSA) promoted solvent-free diversity-oriented synthesis of primary carbamates, S-thiocarbamates and ureas

A simple and highly efficient solvent-free method for the conversion of alcohols, phenols, thiols and amines to primary carbamates, S-thiocarbamates and ureas in the presence of 4-dodecylbenzenesulfonic acid (DBSA) as a cheap and green Bronsted acid reagent has been described. All products were obtained in good to excellent yields and characterized using FT-IR, 1H- and 13C-NMR, MS and CHNS techniques.