1-Bromo-5-chloro-2-fluoro-4-iodobenzene

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Reagent Code: #129276
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CAS Number 1000572-73-5

science Other reagents with same CAS 1000572-73-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 335.34 g/mol
Formula C₆H₂BrClFI
badge Registry Numbers
MDL Number MFCD09878157
thermostat Physical Properties
Boiling Point 273.7±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.331±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of advanced organic molecules, particularly in pharmaceuticals and agrochemicals. Its multiple halogen atoms allow selective cross-coupling reactions, enabling the construction of complex aromatic structures. Commonly employed in Suzuki, Stille, and Ullmann reactions to form carbon-carbon bonds. Also utilized in materials science for developing organic semiconductors and liquid crystals due to its ability to fine-tune electronic properties. The presence of different halogens offers stepwise functionalization, making it valuable in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,590.00
inventory 1g
10-20 days ฿7,140.00
inventory 5g
10-20 days ฿28,390.00

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1-Bromo-5-chloro-2-fluoro-4-iodobenzene
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Used as a key intermediate in the synthesis of advanced organic molecules, particularly in pharmaceuticals and agrochemicals. Its multiple halogen atoms allow selective cross-coupling reactions, enabling the construction of complex aromatic structures. Commonly employed in Suzuki, Stille, and Ullmann reactions to form carbon-carbon bonds. Also utilized in materials science for developing organic semiconductors and liquid crystals due to its ability to fine-tune electronic properties. The presence of diff

Used as a key intermediate in the synthesis of advanced organic molecules, particularly in pharmaceuticals and agrochemicals. Its multiple halogen atoms allow selective cross-coupling reactions, enabling the construction of complex aromatic structures. Commonly employed in Suzuki, Stille, and Ullmann reactions to form carbon-carbon bonds. Also utilized in materials science for developing organic semiconductors and liquid crystals due to its ability to fine-tune electronic properties. The presence of different halogens offers stepwise functionalization, making it valuable in multi-step synthetic routes.

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