76092-29-0

Basic information

• Product Name: 1-BROMO-4-(TRIBROMOMETHYL) BENZENE
• Synonyms: 1-BROMO-4-(TRIBROMOMETHYL) BENZENE;p-Bromotribromotoluene;4-(Tribromomethyl)-bromobenzene
• CAS NO: 76092-29-0
• Molecular Formula: C₇H₄Br₄
• Molecular Weight: 407.72
• Mol File: 76092-29-0.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 328.9 °C at 760 mmHg
• Flash Point: 149.3 °C
• Appearance: /
• Density: 2.511g/cm³
• Vapor Pressure: 0.000351mmHg at 25°C
• Refractive Index: 1.684
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-BROMO-4-(TRIBROMOMETHYL) BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BROMO-4-(TRIBROMOMETHYL) BENZENE(76092-29-0)
• EPA Substance Registry System: 1-BROMO-4-(TRIBROMOMETHYL) BENZENE(76092-29-0)

Safety Data

• Hazardous Substances Data: 76092-29-0(Hazardous Substances Data)

Usage

General Description

1-Bromo-4-(tribromomethyl) benzene is a chemical compound composed of a benzene ring with a bromine atom and a tribromomethyl group attached to it. It is a brominated aromatic compound with potential use as a flame retardant. 1-BROMO-4-(TRIBROMOMETHYL) BENZENE is produced by the bromination of 4-methylbenzoyl chloride with tribromomethane in the presence of aluminum trichloride. It is primarily used as a reactive intermediate in the synthesis of dyes, pharmaceuticals, and other organic compounds. Additionally, it can be used in the production of polymers and as a precursor to other brominated chemicals. However, it is important to handle and store this compound with caution due to its potential hazardous properties.

InChI:InChI=1/C7H4Br4/c8-6-3-1-5(2-4-6)7(9,10)11/h1-4H

Upstream product

• 106-38-7 para-bromotoluene 
• 402-43-7 p-trifluoromethylphenyl bromide 

Downstream Products

• 1222094-28-1 2-(4-bromo-phenyl)-quinazoline 
• 24572-44-9 p-BrC₆H₄(SCF₃)3 
• 108769-94-4 4-Heptyl-1-(4-trifluoromethyl-phenyl)-cyclohexanol 
• 108769-91-1 4-Heptyl-1-(4-trifluoromethyl-phenyl)-cyclohexanol 
• 108769-93-3 4-Pentyl-1-(4-trifluoromethyl-phenyl)-cyclohexanol 
• 108769-90-0 4-Pentyl-1-(4-trifluoromethyl-phenyl)-cyclohexanol 
• 108769-92-2 4-(2-Methyl-butyl)-1-(4-trifluoromethyl-phenyl)-cyclohexanol 
• 108769-89-7 4-(2-Methyl-butyl)-1-(4-trifluoromethyl-phenyl)-cyclohexanol 
• 78238-16-1 α,α',4,4'-tetrabromostilbene 
• 2358-32-9 1-bromo-4-(bromodifluoromethyl)benzene 
• 402-43-7 p-trifluoromethylphenyl bromide 

Relevant articles and documents

On-surface synthesis of graphyne nanowires through stepwise reactions

From an interplay of high-resolution UHV-STM imaging and DFT calculations, we have achieved on-surface synthesis of graphyne nanowires through stepwise reactions involving two different types of dehalogenative homocoupling reactions (i.e., C(sp3/sup

Base-Promoted Synthesis of 2-Aryl Quinazolines from 2-Aminobenzylamines in Water

A transition-metal-free procedure for the synthesis of a highly valuable class of heteroaromatics, quinazolines, was developed by using easily available 2-aminobenzylamines and α,α,α-trihalotoluenes. The transformation proceeded smoothly in the presence of only sodium hydroxide and molecular oxygen in water at 100 °C, furnishing a variety of 2-aryl quinazolines. The crystallization process of the crude reaction mixture for the purification of the solid products circumvents huge solvent-consuming workup and column chromatographic techniques, which make the overall process more sustainable and economical.

Photothermal Side-Chain Bromination of Methyl-, Dimethyl-, and Trimethylbenzenes with N-Bromosuccinimide

Tri- and dibromination of methyl-, dimethyl-, and trimethylbenzenes with N-bromosuccinimide were accomplished by photothermal reaction with a tungsten lamp in carbon tetrachloride or benzene. (Dibromomethyl)arenes and (tribromomethyl) derivatives were produced depending upon a solvent used and a substituent on the benzene ring.In the bromination of methylbenzenes without a substituent on the ortho-position, (tribromomethyl)benzenes were formed.On the other hand, ortho-substituted methylbenzenes gave (dibromomethyl)benzenes. α,β-Dibromo-1,2-diarylstilbenes were formed via the debrominative carbon-carbon coupling reaction of ...