103724-99-8

Basic information

• Product Name: 4-Chloro-2,6-diMethylbroMo benzene
• Synonyms: 4-Chloro-2,6-diMethylbroMo benzene;2-BroMo-5-chloro-1,3-diMethylbebzene;4-Chloro-2,6-dimethylphenyl bromide;4-Chloro-2,6-diMethylbroMobenzene[2-BroMo-5-chloro-1,3-diMethylbenzene]
• CAS NO: 103724-99-8
• Molecular Formula: C₈H₈BrCl
• Molecular Weight: 220
• EINECS: 200-258-5
• Mol File: 103724-99-8.mol
• Article Data: 4

Chemical Properties

• Melting Point: 22-23℃
• Boiling Point: 243.5℃
• Flash Point: 119.9℃
• Appearance: /
• Density: 1.462
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-Chloro-2,6-diMethylbroMo benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Chloro-2,6-diMethylbroMo benzene(103724-99-8)
• EPA Substance Registry System: 4-Chloro-2,6-diMethylbroMo benzene(103724-99-8)

Safety Data

• Hazardous Substances Data: 103724-99-8(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Synthesis, p. 647, 1985 DOI: 10.1055/s-1985-31292

Upstream product

• 75-25-2 Bromoform 
• 103724-96-5 4,4-Dichloro-1,2-dimethylcyclopentene 
• 24596-18-7 4-chloro-2,6-dimethylaniline 

Downstream Products

• 6045-90-5 4-chloro-2,6-dimethylbenzaldehyde 
• 332179-32-5 4-chloro-2,6-dimethylbenzyl alcohol 
• 1315482-74-6 ethyl 2-(4-chloro-2,6-dimethylphenyl)acetate 
• 1610475-25-6 2,6-bis(4-chloro-2,6-dimethylphenyl)pyridine 
• 1374578-82-1 2-(4-chloro-2,6-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 186748-50-5 2-(4-chloro-2,6-dimethylphenyl)acetic acid 

Relevant articles and documents

Process for Preparing Chloro-and Bromoaromatics

The present invention relates to a novel process for preparing chloro- or bromoaromatics of the formula (II) by diazotizing the formula (I) by means of sodium nitrite or potassium nitrite in the presence of aqueous hydrochloric or hydrobromic acids and then reacting with an iron(II) or iron(III) compound, optionally in the presence of additional amounts of hydrogen chloride or hydrogen bromide or alkali metal or alkaline earth metal chlorides or bromides.

Amino substituted pyrazolo[1,5,-a]-1,5-pyrimidines and pyrazolo[1,5-a]-1,3,5-triazines

Disclosed are compounds of the formula: where R1, R2, R3, R4, R5, R6, and X are defined herein. These compounds are selective modulators of NPY1 receptors. These compounds are useful in the