2,5-Difluorobenzyl bromide

98%

Reagent Code: #115389
label
Alias 2,5-Difluorobenzyl bromide 2,5-Difluorobenzyl bromide α-Bromo-2,5-difluorotoluene
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CAS Number 85117-99-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.02 g/mol
Formula C₇H₅BrF₂
badge Registry Numbers
EC Number 285-651-0
MDL Number MFCD00009897
inventory_2 Storage & Handling
Density 1.609 g/mL at 25 °C(lit.)
Storage room temperature, flammable area

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its reactive benzyl bromide group allows for efficient alkylation reactions, making it valuable in constructing complex molecules. Additionally, it is employed in the development of fluorine-containing compounds, which are often sought after for their enhanced stability and bioavailability in drug design. The difluoro substitution on the benzene ring further contributes to its utility in creating materials with specific electronic properties, useful in advanced material science applications.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (HPLC) 98
Refractive Index (N20/D) 1.525-1.528
Specific Gravity (20/20°C) 1.632-1.638
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 ฿340.00
inventory 25g
10-20 days ฿1,900.00
inventory 5g
10-20 days ฿430.00
2,5-Difluorobenzyl bromide
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its reactive benzyl bromide group allows for efficient alkylation reactions, making it valuable in constructing complex molecules. Additionally, it is employed in the development of fluorine-containing compounds, which are often sought after for their enhanced stability and bioavailability in drug design. The difluoro substitution on the benzene ring further contributes to its utility in creating materials with specific electronic properties, useful in advanced material science applications.
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