2-Fluoro-4-(trifluoromethyl)benzoyl chloride

98%

Reagent Code: #116140
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CAS Number 126917-10-0

science Other reagents with same CAS 126917-10-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.56 g/mol
Formula C₈H₃ClF₄O
badge Registry Numbers
MDL Number MFCD00061155
thermostat Physical Properties
Boiling Point 188-189 °C (lit.)
inventory_2 Storage & Handling
Density 1.5 g/mL at 25 °C (lit.)
Storage room temperature

description Product Description

Used primarily as an intermediate in organic synthesis, this compound plays a crucial role in the production of various pharmaceuticals and agrochemicals. Its reactive acyl chloride group enables it to participate in Friedel-Crafts acylation reactions, forming complex aromatic ketones. These ketones are valuable building blocks in the development of active pharmaceutical ingredients (APIs), particularly in drugs targeting central nervous system disorders and anti-inflammatory agents. Additionally, its trifluoromethyl group enhances the metabolic stability and bioavailability of the final compounds, making it a preferred choice in drug design. In agrochemicals, it contributes to the synthesis of herbicides and pesticides, where the fluorine atoms improve efficacy and environmental persistence. Its applications also extend to materials science, where it is used in the preparation of specialty polymers and coatings with unique properties such as chemical resistance and durability.

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Test Parameter Specification
APPEARANCE Colorless to Yellow Liquid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,186.00
inventory 5g
10-20 days ฿9,459.00

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2-Fluoro-4-(trifluoromethyl)benzoyl chloride
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Used primarily as an intermediate in organic synthesis, this compound plays a crucial role in the production of various pharmaceuticals and agrochemicals. Its reactive acyl chloride group enables it to participate in Friedel-Crafts acylation reactions, forming complex aromatic ketones. These ketones are valuable building blocks in the development of active pharmaceutical ingredients (APIs), particularly in drugs targeting central nervous system disorders and anti-inflammatory agents. Additionally, its tr

Used primarily as an intermediate in organic synthesis, this compound plays a crucial role in the production of various pharmaceuticals and agrochemicals. Its reactive acyl chloride group enables it to participate in Friedel-Crafts acylation reactions, forming complex aromatic ketones. These ketones are valuable building blocks in the development of active pharmaceutical ingredients (APIs), particularly in drugs targeting central nervous system disorders and anti-inflammatory agents. Additionally, its trifluoromethyl group enhances the metabolic stability and bioavailability of the final compounds, making it a preferred choice in drug design. In agrochemicals, it contributes to the synthesis of herbicides and pesticides, where the fluorine atoms improve efficacy and environmental persistence. Its applications also extend to materials science, where it is used in the preparation of specialty polymers and coatings with unique properties such as chemical resistance and durability.

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