4-Fluoro-3-methylbenzoyl chloride

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Reagent Code: #77244
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CAS Number 455-84-5

science Other reagents with same CAS 455-84-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.58 g/mol
Formula FC₆H₃CH₃COCl
badge Registry Numbers
MDL Number MFCD01631426
thermostat Physical Properties
Melting Point 115 ° C /2.7kPa
Boiling Point 129-133 °C/17 mmHg(lit.)
inventory_2 Storage & Handling
Density 1.28
Storage Store at 2-8°C, filled with argon

description Product Description

This chemical is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a key building block for creating compounds with specific biological activities, such as anti-inflammatory or antimicrobial agents. Additionally, it is employed in the development of specialty chemicals, including dyes and pigments, due to its reactive benzoyl chloride group. Its fluorine and methyl substituents enhance the stability and reactivity of the resulting products, making it valuable in fine chemical manufacturing.

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inventory 1g
10-20 days ฿1,665.00

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4-Fluoro-3-methylbenzoyl chloride
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This chemical is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a key building block for creating compounds with specific biological activities, such as anti-inflammatory or antimicrobial agents. Additionally, it is employed in the development of specialty chemicals, including dyes and pigments, due to its reactive benzoyl chloride group. Its fluorine and methyl substituents enhance the stability and reactivity of

This chemical is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a key building block for creating compounds with specific biological activities, such as anti-inflammatory or antimicrobial agents. Additionally, it is employed in the development of specialty chemicals, including dyes and pigments, due to its reactive benzoyl chloride group. Its fluorine and methyl substituents enhance the stability and reactivity of the resulting products, making it valuable in fine chemical manufacturing.

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