1-Bromo-4-chloro-2,3-difluorobenzene

98%

Reagent Code: #154448
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CAS Number 1000574-47-9

science Other reagents with same CAS 1000574-47-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.43 g/mol
Formula C₆H₂BrClF₂
badge Registry Numbers
MDL Number MFCD09878201
thermostat Physical Properties
Boiling Point 191.8±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.805±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its halogen substituents allow for selective cross-coupling reactions, making it valuable in building complex molecules for drug discovery. Commonly employed in palladium-catalyzed reactions such as Suzuki and Heck couplings to introduce the difluorobenzene scaffold into target compounds. Also utilized in the preparation of liquid crystals and functional materials where precise electronic and steric properties are required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿590.00
250mg
10-20 days ฿1,050.00
1g
10-20 days ฿3,150.00
5g
10-20 days ฿10,970.00
1-Bromo-4-chloro-2,3-difluorobenzene
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its halogen substituents allow for selective cross-coupling reactions, making it valuable in building complex molecules for drug discovery. Commonly employed in palladium-catalyzed reactions such as Suzuki and Heck couplings to introduce the difluorobenzene scaffold into target compounds. Also utilized in the preparation of liquid crystals and functional materia

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its halogen substituents allow for selective cross-coupling reactions, making it valuable in building complex molecules for drug discovery. Commonly employed in palladium-catalyzed reactions such as Suzuki and Heck couplings to introduce the difluorobenzene scaffold into target compounds. Also utilized in the preparation of liquid crystals and functional materials where precise electronic and steric properties are required.

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