5-Bromo-2-fluoro-3-nitrobenzoic acid

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Reagent Code: #149244
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CAS Number 1153279-80-1

science Other reagents with same CAS 1153279-80-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.01 g/mol
Formula C₇H₃BrFNO₄
badge Registry Numbers
MDL Number MFCD12173024
inventory_2 Storage & Handling
Storage Sealed, dry, room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated and brominated aromatic compounds. Its functional groups enable selective transformations, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build biaryl structures. Also utilized in the preparation of dyes and specialty organic compounds where nitro and halogen substituents are needed for further modification.

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Test Parameter Specification
Appearance Off-white to light yellow solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿310.00
1g
10-20 days ฿1,050.00
5g
10-20 days ฿2,620.00
25g
10-20 days ฿8,600.00
100g
10-20 days ฿34,250.00

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5-Bromo-2-fluoro-3-nitrobenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated and brominated aromatic compounds. Its functional groups enable selective transformations, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build biaryl structures. Also utilized in the preparation of dyes and specialty organic compounds where nitro and halogen substituent
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated and brominated aromatic compounds. Its functional groups enable selective transformations, making it valuable in medicinal chemistry for constructing complex molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to build biaryl structures. Also utilized in the preparation of dyes and specialty organic compounds where nitro and halogen substituents are needed for further modification.
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