2-Bromo-5-cyano-4-picoline

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Reagent Code: #145222
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CAS Number 1003711-35-0

science Other reagents with same CAS 1003711-35-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.03 g/mol
Formula C₇H₅BrN₂
thermostat Physical Properties
Boiling Point 287.9±35.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in building complex organic molecules. Commonly employed in the development of kinase inhibitors and other biologically active compounds. Also utilized in research settings for constructing nitrogen-containing heterocycles, which are prevalent in many drug candidates. The bromo and cyano groups provide reactive sites for cross-coupling reactions, enabling efficient derivatization in medicinal chemistry campaigns.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,180.00
inventory 5g
10-20 days ฿7,140.00
inventory 10g
10-20 days ฿14,280.00

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2-Bromo-5-cyano-4-picoline
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in building complex organic molecules. Commonly employed in the development of kinase inhibitors and other biologically active compounds. Also utilized in research settings for constructing nitrogen-containing heterocycles, which are prevalent in many drug candidates. The bromo and cyano groups provide reactive sites for cross-coupling reactions,

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in building complex organic molecules. Commonly employed in the development of kinase inhibitors and other biologically active compounds. Also utilized in research settings for constructing nitrogen-containing heterocycles, which are prevalent in many drug candidates. The bromo and cyano groups provide reactive sites for cross-coupling reactions, enabling efficient derivatization in medicinal chemistry campaigns.

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