3,5-Difluorobenzyl bromide

98%

Reagent Code: #117266
label
Alias 3,5-Difluorobenzyl bromide 3,5-Difluorobenzyl bromide 3,5-Difluorobenzoyl bromide
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CAS Number 141776-91-2

science Other reagents with same CAS 141776-91-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.02 g/mol
Formula C₇H₅BrF₂
badge Registry Numbers
MDL Number MFCD00010304
thermostat Physical Properties
Boiling Point 65 °C4.5 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.6 g/mL at 25 °C(lit.)
Storage room temperature

description Product Description

3,5-Difluorobenzyl bromide is primarily used as a key intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It is employed in the preparation of various biologically active compounds, including potential drug candidates, due to its ability to introduce the 3,5-difluorobenzyl group into molecules. This group can enhance the metabolic stability and binding affinity of pharmaceutical compounds. Additionally, it is utilized in the development of agrochemicals, such as herbicides and pesticides, where the difluorobenzyl moiety contributes to the efficacy of the final product. Its reactivity as an alkylating agent also makes it valuable in the synthesis of complex organic molecules for research and industrial applications.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 98
Refractive Index (N20/D) 1.518-1.522
Specific Gravity (20/20 °C) 1.617-1.626
Appearance Colorless to Yellow Liquid
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿490.00
inventory 25g
10-20 days ฿2,250.00

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3,5-Difluorobenzyl bromide
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3,5-Difluorobenzyl bromide is primarily used as a key intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It is employed in the preparation of various biologically active compounds, including potential drug candidates, due to its ability to introduce the 3,5-difluorobenzyl group into molecules. This group can enhance the metabolic stability and binding affinity of pharmaceutical compounds. Additionally, it is utilized in the development of agrochemicals, such as herbicides and pesticides, where the difluorobenzyl moiety contributes to the efficacy of the final product. Its reactivity as an alkylating agent also makes it valuable in the synthesis of complex organic molecules for research and industrial applications.
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