2-Bromo-6-iodophenol

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Reagent Code: #149104
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CAS Number 2040-86-0

science Other reagents with same CAS 2040-86-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.910 g/mol
Formula C₆H₄BrIO
badge Registry Numbers
MDL Number MFCD16999870
thermostat Physical Properties
Melting Point 63 °C
Boiling Point 214.4±25.0 °C
inventory_2 Storage & Handling
Density 2.369±0.06 g/cm3
Storage 2-8°C, away from light, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in cross-coupling reactions such as Suzuki or Ullmann reactions where the bromo and iodo groups allow selective functionalization. Also employed in the preparation of liquid crystals and organic semiconductors due to its ability to form complex aromatic structures. Its dual halogen functionality makes it valuable in stepwise synthesis where controlled reactivity is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,400.00
inventory 250mg
10-20 days ฿2,780.00
inventory 1g
10-20 days ฿6,920.00
inventory 5g
10-20 days ฿33,660.00
inventory 10g
10-20 days ฿55,200.00
inventory 25g
10-20 days ฿105,490.00

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2-Bromo-6-iodophenol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in cross-coupling reactions such as Suzuki or Ullmann reactions where the bromo and iodo groups allow selective functionalization. Also employed in the preparation of liquid crystals and organic semiconductors due to its ability to form complex aromatic structures. Its dual halogen functionality makes it valuable in stepwise synthesis where controlled reactivity is required.

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in cross-coupling reactions such as Suzuki or Ullmann reactions where the bromo and iodo groups allow selective functionalization. Also employed in the preparation of liquid crystals and organic semiconductors due to its ability to form complex aromatic structures. Its dual halogen functionality makes it valuable in stepwise synthesis where controlled reactivity is required.

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