3-(Trifluoromethyl)benzoyl chloride

98%

Reagent Code: #117505
label
Alias 3-(Trifluoromethyl)benzoyl chloride; m-trifluoromethylbenzoyl chloride
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CAS Number 2251-65-2

science Other reagents with same CAS 2251-65-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.56 g/mol
Formula C₈H₄ClF₃O
badge Registry Numbers
EC Number 218-844-5
MDL Number MFCD00000680
thermostat Physical Properties
Boiling Point 184-186 °C750 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.383 g/mL at 25 °C(lit.)
Storage room temperature

description Product Description

Primarily used in organic synthesis, this compound serves as a key intermediate for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its reactive acyl chloride group makes it valuable for introducing the 3-(trifluoromethyl)benzoyl moiety into target molecules, enhancing their biological activity or chemical properties. In pharmaceuticals, it is employed in the synthesis of active ingredients, particularly those requiring trifluoromethyl groups for improved metabolic stability and binding affinity. In agrochemicals, it contributes to the development of herbicides and pesticides with enhanced efficacy. Additionally, it finds use in the preparation of dyes, polymers, and other advanced materials, where the trifluoromethyl group imparts unique characteristics such as increased hydrophobicity or chemical resistance.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 98-100%
Refractive Index (N20/D) 1.476-1.478
Specific Gravity (20/20°C) 1.411-1.414
Appearance Colorless to Yellow Liquid
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿440.00
inventory 500g
10-20 days ฿14,140.00
inventory 25g
10-20 days ฿1,110.00
inventory 100g
10-20 days ฿3,490.00

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3-(Trifluoromethyl)benzoyl chloride
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Primarily used in organic synthesis, this compound serves as a key intermediate for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its reactive acyl chloride group makes it valuable for introducing the 3-(trifluoromethyl)benzoyl moiety into target molecules, enhancing their biological activity or chemical properties. In pharmaceuticals, it is employed in the synthesis of active ingredients, particularly those requiring trifluoromethyl groups for improved metabolic stab

Primarily used in organic synthesis, this compound serves as a key intermediate for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its reactive acyl chloride group makes it valuable for introducing the 3-(trifluoromethyl)benzoyl moiety into target molecules, enhancing their biological activity or chemical properties. In pharmaceuticals, it is employed in the synthesis of active ingredients, particularly those requiring trifluoromethyl groups for improved metabolic stability and binding affinity. In agrochemicals, it contributes to the development of herbicides and pesticides with enhanced efficacy. Additionally, it finds use in the preparation of dyes, polymers, and other advanced materials, where the trifluoromethyl group imparts unique characteristics such as increased hydrophobicity or chemical resistance.

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