2-Chloro-6-iodo-3-methylpyridine

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Reagent Code: #130968
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CAS Number 1133961-30-4

science Other reagents with same CAS 1133961-30-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.47 g/mol
Formula C₆H₅ClIN
badge Registry Numbers
MDL Number MFCD28666748
thermostat Physical Properties
Melting Point 60.6 °C
Boiling Point 272.7±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.906±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and other central nervous system agents. It serves as a building block in agrochemicals for the production of certain herbicides and insecticides due to its halogen reactivity enabling cross-coupling reactions. Also employed in research settings for the preparation of pyridine-based ligands and catalysts. Its structure allows selective functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿110,480.00
inventory 1g
10-20 days ฿276,850.00
inventory 100mg
10-20 days ฿64,970.00

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2-Chloro-6-iodo-3-methylpyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and other central nervous system agents. It serves as a building block in agrochemicals for the production of certain herbicides and insecticides due to its halogen reactivity enabling cross-coupling reactions. Also employed in research settings for the preparation of pyridine-based ligands and catalysts. Its structure allows selective functionalization, making it valuable in medi

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and other central nervous system agents. It serves as a building block in agrochemicals for the production of certain herbicides and insecticides due to its halogen reactivity enabling cross-coupling reactions. Also employed in research settings for the preparation of pyridine-based ligands and catalysts. Its structure allows selective functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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