3-bromo-5-methylpyridine-2-carbonitrile

≥95%

Reagent Code: #144188
label
Alias 2-cyano-3-bromo-5-methylpyridine; 3-bromo-5-methylpyridinenitrile; 3-bromo-5-methyl-2-cyanopyridine
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CAS Number 474824-78-7

science Other reagents with same CAS 474824-78-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.03 g/mol
Formula C₇H₅BrN₂
badge Registry Numbers
MDL Number MFCD16988815
thermostat Physical Properties
Boiling Point 321.0±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.61±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in creating targeted drug candidates. Commonly employed in agrochemical research for designing new pesticides and herbicides due to its ability to enhance binding affinity with biological targets. Also utilized in materials science for constructing nitrogen-containing heterocyclic systems in organic electronics.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,830.00
inventory 1g
10-20 days ฿9,070.00
inventory 5g
10-20 days ฿29,640.00

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3-bromo-5-methylpyridine-2-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in creating targeted drug candidates. Commonly employed in agrochemical research for designing new pesticides and herbicides due to its ability to enhance binding affinity with biological targets. Also utilized in materials science for constructing nitrogen-containing heterocyc

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in creating targeted drug candidates. Commonly employed in agrochemical research for designing new pesticides and herbicides due to its ability to enhance binding affinity with biological targets. Also utilized in materials science for constructing nitrogen-containing heterocyclic systems in organic electronics.

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