5-Bromo-1-fluoro-3-methyl-2-nitrobenzene

95%

Reagent Code: #120063
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CAS Number 1224629-03-1

science Other reagents with same CAS 1224629-03-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.02 g/mol
Formula C₇H₅BrFNO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its unique structure allows for selective functionalization, making it valuable in the development of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create biologically active compounds. Additionally, it is utilized in the synthesis of dyes and pigments due to its nitro and halogen substituents, which contribute to color and stability. Its role in material science includes the development of advanced polymers and coatings.

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Test Parameter Specification
Appearance Off-white to Light Yellow Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,283.00
inventory 250mg
10-20 days ฿1,467.00

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5-Bromo-1-fluoro-3-methyl-2-nitrobenzene
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its unique structure allows for selective functionalization, making it valuable in the development of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create biologically active compounds. Additionally, it is utilized in the synthesis of dyes and pigments due to its nitro and halogen substituent

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its unique structure allows for selective functionalization, making it valuable in the development of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, to create biologically active compounds. Additionally, it is utilized in the synthesis of dyes and pigments due to its nitro and halogen substituents, which contribute to color and stability. Its role in material science includes the development of advanced polymers and coatings.

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