2-Chloro-3-fluoropyridine

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Reagent Code: #158396
label
Alias 2-Chloro-3-Fluoropyridine
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CAS Number 17282-04-1

science Other reagents with same CAS 17282-04-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 131.54 g/mol
Formula C₅H₃ClFN
badge Registry Numbers
MDL Number MFCD03095302
thermostat Physical Properties
Boiling Point 80 °C80 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.323 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its structure allows for selective functionalization, making it valuable in creating herbicides, insecticides, and fungicides.

Also employed in the preparation of kinase inhibitors and other biologically active compounds in medicinal chemistry research. Its halogen groups enable cross-coupling reactions, facilitating the construction of complex molecules in drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿132.00
5g
10-20 days ฿410.00
25g
10-20 days ฿850.00
100g
10-20 days ฿3,300.00
2-Chloro-3-fluoropyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its structure allows for selective functionalization, making it valuable in creating herbicides, insecticides, and fungicides.

Also employed in the preparation of kinase inhibitors and other biologically active compounds in medicinal chemistry research. Its halogen groups enable cross-coupling reactions, facilitating the construction of compl

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its structure allows for selective functionalization, making it valuable in creating herbicides, insecticides, and fungicides.

Also employed in the preparation of kinase inhibitors and other biologically active compounds in medicinal chemistry research. Its halogen groups enable cross-coupling reactions, facilitating the construction of complex molecules in drug discovery.

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