6-Bromo-3-chloro-2-methylpyridine

95%

Reagent Code: #145041
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CAS Number 944317-27-5

science Other reagents with same CAS 944317-27-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.47 g/mol
Formula C₆H₅BrClN
thermostat Physical Properties
Boiling Point 222°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and insecticides. Its halogenated pyridine structure enables selective functionalization, making it valuable in creating active ingredients with high biological activity. It is also employed in the preparation of kinase inhibitors and other medicinal compounds where the pyridine ring serves as a core scaffold. Its reactivity allows for cross-coupling reactions, facilitating the construction of complex molecules in drug discovery and crop protection chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿750.00
inventory 1g
10-20 days ฿2,230.00
inventory 5g
10-20 days ฿10,870.00
inventory 10g
10-20 days ฿20,300.00
inventory 25g
10-20 days ฿47,240.00

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6-Bromo-3-chloro-2-methylpyridine
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and insecticides. Its halogenated pyridine structure enables selective functionalization, making it valuable in creating active ingredients with high biological activity. It is also employed in the preparation of kinase inhibitors and other medicinal compounds where the pyridine ring serves as a core scaffold. Its reactivity allows for cross-coupling reactions, facilitating the

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and insecticides. Its halogenated pyridine structure enables selective functionalization, making it valuable in creating active ingredients with high biological activity. It is also employed in the preparation of kinase inhibitors and other medicinal compounds where the pyridine ring serves as a core scaffold. Its reactivity allows for cross-coupling reactions, facilitating the construction of complex molecules in drug discovery and crop protection chemistry.

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