5-bromo-3-(trifluoromethyl)-2-methoxypyridine

98%

Reagent Code: #144030
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CAS Number 1214377-42-0

science Other reagents with same CAS 1214377-42-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.02 g/mol
Formula C₇H₅BrF₃NO
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MDL Number MFCD13185815
inventory_2 Storage & Handling
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) targeting central nervous system disorders. Its structure enables selective functionalization, making it valuable in building complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations for constructing carbon-carbon and carbon-nitrogen bonds. Also utilized in the preparation of kinase inhibitors and herbicides due to its electron-withdrawing trifluoromethyl and bromo groups that enhance reactivity and binding affinity.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,270.00
inventory 10g
10-20 days ฿2,480.00
inventory 25g
10-20 days ฿5,030.00
inventory 50g
10-20 days ฿9,810.00

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5-bromo-3-(trifluoromethyl)-2-methoxypyridine
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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) targeting central nervous system disorders. Its structure enables selective functionalization, making it valuable in building complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations for constructing carbon-carbon and carbon-nitrogen bonds. Also utilized in the preparation of kinase

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs) targeting central nervous system disorders. Its structure enables selective functionalization, making it valuable in building complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations for constructing carbon-carbon and carbon-nitrogen bonds. Also utilized in the preparation of kinase inhibitors and herbicides due to its electron-withdrawing trifluoromethyl and bromo groups that enhance reactivity and binding affinity.

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