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1-Bromo-3,5-diethylbenzene functions as a substrate in organic synthesis. It acts as an electrophile in Friedel-Crafts alkylation reactions, where it undergoes substitution reactions with aromatic compounds in the presence of a Lewis acid catalyst. 1-Bromo-3,5-Diethylbenzene′s mechanism of action involves the formation of a carbocation intermediate, which then reacts with the aromatic compound to form a new carbon-carbon bond. This process allows for the introduction of the 1-bromo-3,5-diethylbenzene moiety into the target molecule, enabling the synthesis of complex organic compounds for further study and analysis. Its role in these reactions contributes to the development of new materials and other organic compounds of interest in development applications.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-Bromo-3,5-diethylbenzene, 1 g | sc-282050 | 1 g | $48.00 | |||
1-Bromo-3,5-diethylbenzene, 5 g | sc-282050A | 5 g | $129.00 |