2,3,4-Trifluorobenzoyl chloride

98%

Reagent Code: #57824
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CAS Number 157373-08-5

science Other reagents with same CAS 157373-08-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.53 g/mol
Formula C₇H₂ClF₃O
badge Registry Numbers
MDL Number MFCD00075078
thermostat Physical Properties
Boiling Point 143-144 °C130 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.522 g/mL at 25 °C(lit.)
Storage Room temperature, inert gas protection

description Product Description

Used primarily as a key intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is employed in the creation of complex molecules due to its reactive acyl chloride group, which facilitates the formation of amides, esters, and other derivatives. The three fluoro substituents on the benzene ring enhance the biological activity and stability of the resulting compounds, making it valuable in the development of drugs with improved efficacy and metabolic resistance. Additionally, it finds application in material science for synthesizing specialty polymers and coatings with unique properties.

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Test Parameter Specification
Purity 97.5-100%
Appearance Colorless to light yellow liquid
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,080.00
inventory 5g
10-20 days ฿9,180.00

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2,3,4-Trifluorobenzoyl chloride
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Used primarily as a key intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is employed in the creation of complex molecules due to its reactive acyl chloride group, which facilitates the formation of amides, esters, and other derivatives. The three fluoro substituents on the benzene ring enhance the biological activity and stability of the resulting compounds, making it valuable in the development of drugs with improved efficacy and metabolic resist

Used primarily as a key intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is employed in the creation of complex molecules due to its reactive acyl chloride group, which facilitates the formation of amides, esters, and other derivatives. The three fluoro substituents on the benzene ring enhance the biological activity and stability of the resulting compounds, making it valuable in the development of drugs with improved efficacy and metabolic resistance. Additionally, it finds application in material science for synthesizing specialty polymers and coatings with unique properties.

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