1-(Bromomethyl)-2-chloro-4-(trifluoromethyl)benzene

95%

Reagent Code: #130642
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CAS Number 279252-26-5

science Other reagents with same CAS 279252-26-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.48 g/mol
Formula C₈H₅BrClF₃
badge Registry Numbers
MDL Number MFCD14155638
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its reactive bromomethyl and chloro groups allow for selective functionalization, making it valuable in building complex organic molecules. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce the trifluoromethylphenyl moiety, which can enhance metabolic stability and lipophilicity in active ingredients. Widely applied in research and industrial settings for creating herbicides, fungicides, and medicinal agents targeting central nervous system disorders and inflammation.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,750.00
inventory 1g
10-20 days ฿23,400.00
inventory 100mg
10-20 days ฿5,460.00

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1-(Bromomethyl)-2-chloro-4-(trifluoromethyl)benzene
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its reactive bromomethyl and chloro groups allow for selective functionalization, making it valuable in building complex organic molecules. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce the trifluoromethylphenyl moiety, which can enhance metabolic stability and lipophilicity in active ingredients. Widely applie

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its reactive bromomethyl and chloro groups allow for selective functionalization, making it valuable in building complex organic molecules. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce the trifluoromethylphenyl moiety, which can enhance metabolic stability and lipophilicity in active ingredients. Widely applied in research and industrial settings for creating herbicides, fungicides, and medicinal agents targeting central nervous system disorders and inflammation.

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