4-(Bromomethyl)-2-(trifluoromethyl)pyridine

96%

Reagent Code: #150880
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CAS Number 1227585-56-9

science Other reagents with same CAS 1227585-56-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.02 g/mol
Formula C₇H₅BrF₃N
badge Registry Numbers
MDL Number MFCD15526799
thermostat Physical Properties
Boiling Point 209.1±35.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, inert atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its reactive bromomethyl group allows for easy alkylation or coupling reactions, making it valuable in constructing complex organic structures. Commonly employed in medicinal chemistry for introducing the 2-(trifluoromethyl)pyridine moiety, which can enhance metabolic stability and binding affinity in drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the favorable electronic and lipophilic properties of the trifluoromethylpyridine scaffold.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,490.00
inventory 250mg
10-20 days ฿20,150.00
inventory 1g
10-20 days ฿60,390.00

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4-(Bromomethyl)-2-(trifluoromethyl)pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its reactive bromomethyl group allows for easy alkylation or coupling reactions, making it valuable in constructing complex organic structures. Commonly employed in medicinal chemistry for introducing the 2-(trifluoromethyl)pyridine moiety, which can enhance metabolic stability and binding affinity in drug candidates. Also utilized in agrochemical research fo

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its reactive bromomethyl group allows for easy alkylation or coupling reactions, making it valuable in constructing complex organic structures. Commonly employed in medicinal chemistry for introducing the 2-(trifluoromethyl)pyridine moiety, which can enhance metabolic stability and binding affinity in drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the favorable electronic and lipophilic properties of the trifluoromethylpyridine scaffold.

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