2-(Bromomethyl)-3-fluoropyridine hydrobromide

98%

Reagent Code: #132036
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CAS Number 1427429-75-1

science Other reagents with same CAS 1427429-75-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.92 g/mol
Formula C₆H₆Br₂FN
badge Registry Numbers
MDL Number MFCD22570235
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated pyridine-based drugs. Its reactive bromomethyl group allows for easy coupling in organic reactions, making it valuable in creating active pharmaceutical ingredients (APIs) for treatments targeting neurological disorders and infectious diseases. Commonly employed in alkylation and cross-coupling reactions to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿14,480.00
inventory 5g
10-20 days ฿43,930.00
inventory 250mg
10-20 days ฿5,850.00

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2-(Bromomethyl)-3-fluoropyridine hydrobromide
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated pyridine-based drugs. Its reactive bromomethyl group allows for easy coupling in organic reactions, making it valuable in creating active pharmaceutical ingredients (APIs) for treatments targeting neurological disorders and infectious diseases. Commonly employed in alkylation and cross-coupling reactions to build complex heterocyclic systems. Also utilized in agrochemical research for designing

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated pyridine-based drugs. Its reactive bromomethyl group allows for easy coupling in organic reactions, making it valuable in creating active pharmaceutical ingredients (APIs) for treatments targeting neurological disorders and infectious diseases. Commonly employed in alkylation and cross-coupling reactions to build complex heterocyclic systems. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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