Methyl 5-bromo-2-(trifluoromethyl)isonicotinate

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Reagent Code: #207490
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CAS Number 1211589-41-1

science Other reagents with same CAS 1211589-41-1

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Weight 284.03 g/mol
Formula C₈H₅BrF₃NO₂
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MDL Number MFCD16657895
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 kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amine groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the presence of trifluoromethyl and bromo moieties, which enhance lipophilicity and metabolic stability. Suitable for high-throughput screening and combinatorial chemistry in drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,560.00
inventory 1g
10-20 days ฿5,990.00
inventory 5g
10-20 days ฿21,970.00

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Methyl 5-bromo-2-(trifluoromethyl)isonicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amine groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amine groups. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the presence of trifluoromethyl and bromo moieties, which enhance lipophilicity and metabolic stability. Suitable for high-throughput screening and combinatorial chemistry in drug discovery.

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