2-(bromomethyl)-6-chloropyridine

95%

Reagent Code: #149016
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CAS Number 63763-79-1

science Other reagents with same CAS 63763-79-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.4676 g/mol
Formula C₆H₅BrClN
badge Registry Numbers
MDL Number MFCD07778340
thermostat Physical Properties
Boiling Point 241.089 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.664 g/cm3
Storage -20°C, light-proof, inert atmosphere

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and other bioactive molecules. The bromomethyl group at the 2-position provides high reactivity for nucleophilic substitutions and cross-coupling reactions, allowing the introduction of pyridine-based structures into larger compounds. The 6-chloro substituent enables further functionalization via nucleophilic aromatic substitution, making it valuable in medicinal chemistry for building complex heterocyclic systems. Also utilized in agrochemical research for the design of novel pesticides and herbicides due to the favorable electronic properties of the chloropyridine scaffold.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,320.00
inventory 1g
10-20 days ฿17,030.00

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2-(bromomethyl)-6-chloropyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and other bioactive molecules. The bromomethyl group at the 2-position provides high reactivity for nucleophilic substitutions and cross-coupling reactions, allowing the introduction of pyridine-based structures into larger compounds. The 6-chloro substituent enables further functionalization via nucleophilic aromatic substitution, making it valuable in medicinal chemistry for buildi

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and other bioactive molecules. The bromomethyl group at the 2-position provides high reactivity for nucleophilic substitutions and cross-coupling reactions, allowing the introduction of pyridine-based structures into larger compounds. The 6-chloro substituent enables further functionalization via nucleophilic aromatic substitution, making it valuable in medicinal chemistry for building complex heterocyclic systems. Also utilized in agrochemical research for the design of novel pesticides and herbicides due to the favorable electronic properties of the chloropyridine scaffold.

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