Ethyl 5-bromopyrimidine-2-carboxylate

98%

Reagent Code: #182574
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CAS Number 1197193-30-8

science Other reagents with same CAS 1197193-30-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.05 g/mol
Formula C₇H₇BrN₂O₂
badge Registry Numbers
MDL Number MFCD12964050
inventory_2 Storage & Handling
Storage Room temperature, dry

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 cross-coupling reactions, making it valuable in constructing complex heterocyclic systems found in drug candidates. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce pyrimidine moieties into target molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to modulate biological activity in specific molecular frameworks.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,090.00
5g
10-20 days ฿4,680.00
25g
10-20 days ฿18,970.00
250mg
10-20 days ฿310.00
Ethyl 5-bromopyrimidine-2-carboxylate
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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 cross-coupling reactions, making it valuable in constructing complex heterocyclic systems found in drug candidates. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce pyrimidine moieties into target molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due
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 cross-coupling reactions, making it valuable in constructing complex heterocyclic systems found in drug candidates. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce pyrimidine moieties into target molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to modulate biological activity in specific molecular frameworks.
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