2,4,5-Trifluorobenzyl chloride

Standard for GC, ≥99.7%(GC)

Reagent Code: #238126
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CAS Number 243139-71-1

science Other reagents with same CAS 243139-71-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.56 g/mol
Formula C₇H₄ClF₃
badge Registry Numbers
MDL Number MFCD00236319
thermostat Physical Properties
Boiling Point 175 °C
inventory_2 Storage & Handling
Density 1.689 g/cm3
Storage Room temperature

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive benzyl chloride group enables easy attachment to other molecules, making it valuable in building complex organic structures. Commonly employed in the development of fluorinated active pharmaceutical ingredients (APIs), where the fluorine atoms enhance metabolic stability and binding affinity. Also utilized in the preparation of specialty chemicals, including liquid crystals and functional materials, where fluorine substitution improves thermal and chemical resistance. Its selectivity in substitution reactions allows for precise molecular engineering in research and industrial applications.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿6,200.00
2,4,5-Trifluorobenzyl chloride
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Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive benzyl chloride group enables easy attachment to other molecules, making it valuable in building complex organic structures. Commonly employed in the development of fluorinated active pharmaceutical ingredients (APIs), where the fluorine atoms enhance metabolic stability and binding affinity. Also utilized in the preparation of specialty chemicals, including liquid crystals and functional materials, w

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive benzyl chloride group enables easy attachment to other molecules, making it valuable in building complex organic structures. Commonly employed in the development of fluorinated active pharmaceutical ingredients (APIs), where the fluorine atoms enhance metabolic stability and binding affinity. Also utilized in the preparation of specialty chemicals, including liquid crystals and functional materials, where fluorine substitution improves thermal and chemical resistance. Its selectivity in substitution reactions allows for precise molecular engineering in research and industrial applications.

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