3-Bromo-5-(trifluoromethyl)pyridin-2-amine

98%

Reagent Code: #151311
label
Alias 3-Bromo-2-amino-5-(trifluoromethyl)pyridine
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CAS Number 79456-30-7

science Other reagents with same CAS 79456-30-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.01 g/mol
Formula C₆H₄BrF₃N₂
badge Registry Numbers
MDL Number MFCD07375382
thermostat Physical Properties
Melting Point 98-101 °C
Boiling Point 221.7 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

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 medicinal chemistry for creating analogs with improved potency and selectivity. Commonly employed in cross-coupling reactions to form carbon-nitrogen or carbon-carbon bonds, it supports the construction of complex heterocyclic systems found in drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the presence of trifluoromethyl and bromo groups that enhance lipophilicity and metabolic stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿900.00
inventory 10g
10-20 days ฿1,760.00
inventory 25g
10-20 days ฿4,400.00
inventory 100g
10-20 days ฿15,180.00

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3-Bromo-5-(trifluoromethyl)pyridin-2-amine
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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 medicinal chemistry for creating analogs with improved potency and selectivity. Commonly employed in cross-coupling reactions to form carbon-nitrogen or carbon-carbon bonds, it supports the construction of complex heterocyclic systems found in drug candidates. Also utilized in
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 medicinal chemistry for creating analogs with improved potency and selectivity. Commonly employed in cross-coupling reactions to form carbon-nitrogen or carbon-carbon bonds, it supports the construction of complex heterocyclic systems found in drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the presence of trifluoromethyl and bromo groups that enhance lipophilicity and metabolic stability.
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