75894-99-4

Usage

Structure

A benzene ring with two bromine atoms attached at the 1st and 3rd positions, and an octyl group attached at the 5th position.

Derivative

Benzene

Bromine atoms

Two

Octyl group

One

Usage

Intermediate in the synthesis of other organic compounds, production of specialty chemicals, manufacturing of polymers, and as a reagent in organic chemistry reactions.

Hazard

Harmful if swallowed

Safety precautions

Handle with care and store in a well-ventilated area.

Upstream product

• 1041479-71-3 C₂₄H₅₁In 
• 1205517-08-3 (3,5-dibromophenyl)zinc(II) chloride 
• 1380609-32-4 2,6-dibromo-4-octylaniline 

Downstream Products

• 1427513-93-6 1-bromo-3-iodo-5-octylbenzene 

Relevant academic research and scientific papers

Radical/anionic SRN1-type polymerization for preparation of oligoarenes

Radicals and anions: The TEMPO-mediated oxidation of magnesiated iodoarenes A provides highly regioregular poly(m-phenylenes) by strictly alternating anionic/radical cross-over chain-growth polymerization. Poly(m-phenylenes) with mean molecular weight (M

Highly selective palladium-catalyzed oxidative Csp2-Csp 3 cross-coupling of arylzinc and alkylindium reagents through double transmetallation

Using desyl chloride (2-chloro-1,2-diphenylethanone) as the oxidant, the palladium-catalyzed reaction of arylzinc with alkylindium reagents occurred smoothly in a highly selective manner to afford the products in 57-90% yields. Preliminary kinetic data in