1-Ethyl-4-iodobenzene

98%

Reagent Code: #182957
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CAS Number 25309-64-2

science Other reagents with same CAS 25309-64-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.07 g/mol
Formula C₈H₉I
badge Registry Numbers
MDL Number MFCD00060663
thermostat Physical Properties
Melting Point -17°C
Boiling Point 112-113°C/20mmHg
inventory_2 Storage & Handling
Density 1.6g/mL
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in pharmaceuticals and agrochemicals. It serves as a building block in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the formation of carbon-carbon bonds. The iodine substituent is highly reactive, making it ideal for palladium-catalyzed transformations. It is also employed in the preparation of liquid crystals, dyes, and functionalized aromatic compounds for materials science research. Its ethyl group provides steric and electronic modulation, enhancing selectivity in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿290.00
inventory 25g
10-20 days ฿800.00
inventory 100g
10-20 days ฿3,020.00

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1-Ethyl-4-iodobenzene
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Used primarily as an intermediate in organic synthesis, especially in pharmaceuticals and agrochemicals. It serves as a building block in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the formation of carbon-carbon bonds. The iodine substituent is highly reactive, making it ideal for palladium-catalyzed transformations. It is also employed in the preparation of liquid crystals, dyes, and functionalized aromatic compounds for materials science research. Its ethyl group provides ste

Used primarily as an intermediate in organic synthesis, especially in pharmaceuticals and agrochemicals. It serves as a building block in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the formation of carbon-carbon bonds. The iodine substituent is highly reactive, making it ideal for palladium-catalyzed transformations. It is also employed in the preparation of liquid crystals, dyes, and functionalized aromatic compounds for materials science research. Its ethyl group provides steric and electronic modulation, enhancing selectivity in synthetic pathways.

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