Methyl 5-bromo-2-fluoronicotinate

98%

Reagent Code: #207195
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CAS Number 931105-37-2

science Other reagents with same CAS 931105-37-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.02 g/mol
Formula C₇H₅BrFNO₂
badge Registry Numbers
MDL Number MFCD11617316
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 kinase inhibitors and other bioactive molecules targeting inflammatory and oncological diseases. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds in medicinal chemistry. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig aminations to introduce the nicotinate core into target molecules. Also utilized in agrochemical research for designing new pesticides and herbicides due to its fluorinated and brominated aromatic system, which enhances binding affinity and metabolic stability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,630.00
5g
10-20 days ฿6,670.00
10g
10-20 days ฿12,680.00
25g
10-20 days ฿31,600.00
Methyl 5-bromo-2-fluoronicotinate
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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 targeting inflammatory and oncological diseases. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds in medicinal chemistry. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig aminations to introduce the nicotinate core into target molecules. Also utilize

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules targeting inflammatory and oncological diseases. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds in medicinal chemistry. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig aminations to introduce the nicotinate core into target molecules. Also utilized in agrochemical research for designing new pesticides and herbicides due to its fluorinated and brominated aromatic system, which enhances binding affinity and metabolic stability.

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