4-Fluorobenzyl chloride

98%

Reagent Code: #118943
label
Alias 4-Fluorochlorobenzyl ; p-Fluorochlorobenzyl
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CAS Number 352-11-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 144.57 g/mol
Formula C₇H₆ClF
badge Registry Numbers
EC Number 206-516-4
MDL Number MFCD00000913
thermostat Physical Properties
Melting Point -18 °C
Boiling Point 82 °C26 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.207 g/mL at 25 °C(lit.)
Storage room temperature

description Product Description

Used primarily as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It plays a key role in the production of active pharmaceutical ingredients (APIs) by serving as a building block for more complex molecules. Additionally, it is employed in the development of specialty chemicals, including dyes and pigments, due to its reactivity and ability to introduce fluorobenzyl groups into target compounds. Its application extends to research and development, where it is utilized in organic synthesis to explore new chemical reactions and pathways.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 98-100
Refractive Index (N20/D) 1.512-1.514
Specific Gravity (20/20°C) 1.207-1.212
Appearance Colorless to Yellow Liquid
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 2.5kg
10-20 days ฿14,180.00
inventory 100g
10-20 days ฿970.00
inventory 25g
10-20 days ฿350.00
inventory 500g
10-20 days ฿3,060.00
4-Fluorobenzyl chloride
Used primarily as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It plays a key role in the production of active pharmaceutical ingredients (APIs) by serving as a building block for more complex molecules. Additionally, it is employed in the development of specialty chemicals, including dyes and pigments, due to its reactivity and ability to introduce fluorobenzyl groups into target compounds. Its application extends to research and development, where it is utilized in organic synthesis to explore new chemical reactions and pathways.
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