1,2-Dibromo-4,5-difluoro-3-nitrobenzene

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Reagent Code: #40675
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CAS Number 1481-57-8

science Other reagents with same CAS 1481-57-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.88 g/mol
Formula C₆HBr₂F₂NO₂
badge Registry Numbers
MDL Number MFCD11226312
thermostat Physical Properties
Boiling Point 274.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in organic synthesis as a versatile intermediate for the production of more complex compounds. Its unique structure, featuring bromine, fluorine, and nitro groups, makes it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. It is often employed in cross-coupling reactions, where the bromine atoms facilitate the formation of carbon-carbon bonds, while the nitro group can be reduced or further modified. Additionally, the presence of fluorine atoms enhances the stability and reactivity of the molecule, making it useful in the design of materials with specific electronic or biological properties. Its applications also extend to research and development in medicinal chemistry, where it serves as a building block for drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,888.00
inventory 5g
10-20 days ฿12,420.00
inventory 10g
10-20 days ฿21,114.00

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1,2-Dibromo-4,5-difluoro-3-nitrobenzene
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This chemical is primarily used in organic synthesis as a versatile intermediate for the production of more complex compounds. Its unique structure, featuring bromine, fluorine, and nitro groups, makes it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. It is often employed in cross-coupling reactions, where the bromine atoms facilitate the formation of carbon-carbon bonds, while the nitro group can be reduced or further modified. Additionally, the presence of fluor

This chemical is primarily used in organic synthesis as a versatile intermediate for the production of more complex compounds. Its unique structure, featuring bromine, fluorine, and nitro groups, makes it valuable in the development of pharmaceuticals, agrochemicals, and specialty chemicals. It is often employed in cross-coupling reactions, where the bromine atoms facilitate the formation of carbon-carbon bonds, while the nitro group can be reduced or further modified. Additionally, the presence of fluorine atoms enhances the stability and reactivity of the molecule, making it useful in the design of materials with specific electronic or biological properties. Its applications also extend to research and development in medicinal chemistry, where it serves as a building block for drug discovery.

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