3-bromo-5-fluorobenzaldehyde

95%

Reagent Code: #66307
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CAS Number 188813-02-7

science Other reagents with same CAS 188813-02-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.01 g/mol
Formula C₇H₄BrFO
badge Registry Numbers
MDL Number MFCD04116319
inventory_2 Storage & Handling
Storage room temperature

description Product Description

3-bromo-5-fluorobenzaldehyde is primarily used in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring both bromine and fluorine substituents, makes it valuable in the development of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biologically active compounds. Additionally, it serves as a building block in the synthesis of heterocyclic compounds, which are essential in drug discovery. The presence of the aldehyde group allows for further functionalization, enabling the creation of diverse chemical entities. This compound is particularly useful in medicinal chemistry for designing molecules with potential therapeutic applications.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 94.5-100
Appearance Off-white to yellow solid

Available Sizes & Pricing

Size Availability Unit Price Quantity
25g
10-20 days ฿6,260.00
1g
10-20 days ฿420.00
5g
10-20 days ฿1,660.00
100g
10-20 days ฿18,280.00
3-bromo-5-fluorobenzaldehyde
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3-bromo-5-fluorobenzaldehyde is primarily used in organic synthesis as a key intermediate for the production of various pharmaceuticals and agrochemicals. Its unique structure, featuring both bromine and fluorine substituents, makes it valuable in the development of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create biologically active compounds. Additionally, it serves as a building block in the synthesis of heterocyclic compounds, which are essential in drug discovery. The presence of the aldehyde group allows for further functionalization, enabling the creation of diverse chemical entities. This compound is particularly useful in medicinal chemistry for designing molecules with potential therapeutic applications.
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