2-Bromo-1-(bromomethyl)-3-fluorobenzene

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Reagent Code: #116638
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CAS Number 1184918-22-6

science Other reagents with same CAS 1184918-22-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.92 g/mol
Formula C₇H₅Br₂F
badge Registry Numbers
MDL Number MFCD12911576
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds. Its unique structure, featuring both bromine and fluorine substituents, makes it valuable in the development of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to create aromatic compounds with specific properties. Additionally, it serves as a building block in the production of specialty chemicals, including dyes, pigments, and advanced materials. Its reactivity allows for precise modifications, making it a versatile tool in organic synthesis.

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Test Parameter Specification
Appearance White to Yellow Solid, Powder or Crystals
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,165.00
inventory 250mg
10-20 days ฿729.00
inventory 1g
10-20 days ฿1,755.00
inventory 10g
10-20 days ฿9,405.00

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2-Bromo-1-(bromomethyl)-3-fluorobenzene
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This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds. Its unique structure, featuring both bromine and fluorine substituents, makes it valuable in the development of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to create aromatic compounds with specific properties. Additionally, it serves as a building block in the production of specialty chemicals, including dyes, pigments, and adva

This chemical is primarily used as an intermediate in the synthesis of more complex organic compounds. Its unique structure, featuring both bromine and fluorine substituents, makes it valuable in the development of pharmaceuticals and agrochemicals. It is often employed in cross-coupling reactions, such as Suzuki or Heck reactions, to create aromatic compounds with specific properties. Additionally, it serves as a building block in the production of specialty chemicals, including dyes, pigments, and advanced materials. Its reactivity allows for precise modifications, making it a versatile tool in organic synthesis.

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