Methyl4-bromo-2-fluoro-3-formylbenzoate

98%

Reagent Code: #213850
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CAS Number 2383830-99-5

science Other reagents with same CAS 2383830-99-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.04 g/mol
Formula C₉H₆BrFO₃
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 anti-inflammatory and anticancer agents. Its functional groups—bromine, fluorine, aldehyde, and ester—allow for selective modifications, enabling the construction of complex organic molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions, where the bromine moiety facilitates carbon-carbon bond formation. The aldehyde group can be further derivatized to introduce heterocyclic structures, making it valuable in medicinal chemistry for building bioactive compounds. Also utilized in agrochemical research for designing novel active ingredients due to its structural versatility.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,340.00
250mg
10-20 days ฿9,020.00
5g
10-20 days ฿78,740.00
1g
10-20 days ฿24,230.00
Methyl4-bromo-2-fluoro-3-formylbenzoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and anticancer agents. Its functional groups—bromine, fluorine, aldehyde, and ester—allow for selective modifications, enabling the construction of complex organic molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions, where the bromine moiety facilitates carbon-carbon bond formation. The aldehyde group can be further derivatized to introduce heterocycli

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and anticancer agents. Its functional groups—bromine, fluorine, aldehyde, and ester—allow for selective modifications, enabling the construction of complex organic molecules. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions, where the bromine moiety facilitates carbon-carbon bond formation. The aldehyde group can be further derivatized to introduce heterocyclic structures, making it valuable in medicinal chemistry for building bioactive compounds. Also utilized in agrochemical research for designing novel active ingredients due to its structural versatility.

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