5-Bromo-2-cyano-3-(trifluoromethyl)pyridine

98%

Reagent Code: #145110
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CAS Number 1214377-57-7

science Other reagents with same CAS 1214377-57-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251 g/mol
Formula C₇H₂BrF₃N₂
thermostat Physical Properties
Boiling Point 257°C
inventory_2 Storage & Handling
Storage 2-8°C

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 further functionalization, making it valuable in creating compounds with biological activity. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations due to the presence of bromine and cyano groups. The trifluoromethyl group enhances lipophilicity and metabolic stability in final products, which is beneficial in drug design. Also utilized in the preparation of kinase inhibitors and other targeted therapies in medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿590.00
inventory 250mg
10-20 days ฿800.00
inventory 1g
10-20 days ฿2,690.00
inventory 5g
10-20 days ฿13,360.00
inventory 25g
10-20 days ฿66,750.00

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5-Bromo-2-cyano-3-(trifluoromethyl)pyridine
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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 further functionalization, making it valuable in creating compounds with biological activity. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations due to the presence of bromine and cyano groups. The trifluoromethyl group enhances lipophilicity and metabolic stability in final products

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 further functionalization, making it valuable in creating compounds with biological activity. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations due to the presence of bromine and cyano groups. The trifluoromethyl group enhances lipophilicity and metabolic stability in final products, which is beneficial in drug design. Also utilized in the preparation of kinase inhibitors and other targeted therapies in medicinal chemistry research.

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