2-Fluorobenzyl bromide

97%

Reagent Code: #116187
label
Alias 2-fluorobenzyl bromide; 2-fluorobenzyl bromide, o-fluorobenzyl bromide, 2-fluorobenzyl bromide
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CAS Number 446-48-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.02 g/mol
Formula C₇H₆BrF
badge Registry Numbers
MDL Number MFCD00000324
thermostat Physical Properties
Boiling Point 84-85 °C15 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.567 g/mL at 25 °C(lit.)
Storage room temperature

description Product Description

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the production of pharmaceuticals and agrochemicals. It is particularly valuable in the synthesis of fluorinated aromatic compounds, which are often incorporated into drugs to enhance their metabolic stability and bioavailability. Additionally, it serves as a building block in the development of specialty chemicals, including dyes and fragrances. Its reactivity with various nucleophiles makes it a versatile reagent in cross-coupling reactions, enabling the creation of complex molecular structures.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 97-100
Refractive Index (N20/D) 1.549-1.553
Specific Gravity (20/20°C) 1.538-1.552
Appearance Colorless to light yellow liquid
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500g
10-20 days ฿16,020.00
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿840.00
inventory 100g
10-20 days ฿3,290.00
2-Fluorobenzyl bromide
Used primarily as an intermediate in organic synthesis, this compound plays a key role in the production of pharmaceuticals and agrochemicals. It is particularly valuable in the synthesis of fluorinated aromatic compounds, which are often incorporated into drugs to enhance their metabolic stability and bioavailability. Additionally, it serves as a building block in the development of specialty chemicals, including dyes and fragrances. Its reactivity with various nucleophiles makes it a versatile reagent in cross-coupling reactions, enabling the creation of complex molecular structures.
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