1-Iodo-4-propoxybenzene

95%

Reagent Code: #198557
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CAS Number 95306-89-1

science Other reagents with same CAS 95306-89-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.09 g/mol
Formula C₉H₁₁IO
badge Registry Numbers
MDL Number MFCD00505983
thermostat Physical Properties
Boiling Point 268.2±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.555±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the formation of carbon-carbon bonds. Its iodo functionality provides high reactivity in palladium-catalyzed transformations, making it valuable in the development of liquid crystals, agrochemicals, and functional materials. Also employed in the synthesis of propofol derivatives and other bioactive compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿6,600.00
inventory 100mg
10-20 days ฿19,800.00
inventory 250mg
10-20 days ฿36,500.00

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1-Iodo-4-propoxybenzene
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the formation of carbon-carbon bonds. Its iodo functionality provides high reactivity in palladium-catalyzed transformations, making it valuable in the development of liquid crystals, agrochemicals, and functional materials. Also employed in the synthesis of propofol derivatives and other

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the formation of carbon-carbon bonds. Its iodo functionality provides high reactivity in palladium-catalyzed transformations, making it valuable in the development of liquid crystals, agrochemicals, and functional materials. Also employed in the synthesis of propofol derivatives and other bioactive compounds.

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