2,5-Bis(trifluoromethyl)benzoyl chloride

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Reagent Code: #77069
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CAS Number 393-82-8

science Other reagents with same CAS 393-82-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.56 g/mol
Formula CF₃₂C₆H₃COCl
badge Registry Numbers
MDL Number MFCD00074997
inventory_2 Storage & Handling
Density 1.5280
Storage Store at 2-8°C, filled with argon

description Product Description

Used primarily in organic synthesis, this chemical serves as a key reagent for introducing trifluoromethyl groups into various compounds. Its reactivity with nucleophiles makes it valuable in the production of pharmaceuticals, particularly in the development of drugs with enhanced metabolic stability and bioavailability. Additionally, it is employed in the synthesis of agrochemicals, where the trifluoromethyl group improves the efficacy and selectivity of pesticides and herbicides. In material science, it is utilized to modify polymers and coatings, imparting properties such as increased chemical resistance and durability. Its role in creating advanced intermediates for fine chemicals and specialty materials further highlights its versatility in industrial applications.

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inventory 1g
10-20 days ฿3,132.00

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2,5-Bis(trifluoromethyl)benzoyl chloride
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Used primarily in organic synthesis, this chemical serves as a key reagent for introducing trifluoromethyl groups into various compounds. Its reactivity with nucleophiles makes it valuable in the production of pharmaceuticals, particularly in the development of drugs with enhanced metabolic stability and bioavailability. Additionally, it is employed in the synthesis of agrochemicals, where the trifluoromethyl group improves the efficacy and selectivity of pesticides and herbicides. In material science, i

Used primarily in organic synthesis, this chemical serves as a key reagent for introducing trifluoromethyl groups into various compounds. Its reactivity with nucleophiles makes it valuable in the production of pharmaceuticals, particularly in the development of drugs with enhanced metabolic stability and bioavailability. Additionally, it is employed in the synthesis of agrochemicals, where the trifluoromethyl group improves the efficacy and selectivity of pesticides and herbicides. In material science, it is utilized to modify polymers and coatings, imparting properties such as increased chemical resistance and durability. Its role in creating advanced intermediates for fine chemicals and specialty materials further highlights its versatility in industrial applications.

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