Ethyl 4-Iodobenzoate

98%

Reagent Code: #181586
label
Alias 4-Iodine Benzoate
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CAS Number 51934-41-9

science Other reagents with same CAS 51934-41-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.07 g/mol
Formula C₉H₉IO₂
badge Registry Numbers
MDL Number MFCD00017344
thermostat Physical Properties
Boiling Point 281-283 °C
inventory_2 Storage & Handling
Density 1.641 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly 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 allows for selective functionalization, making it valuable in the preparation of complex aromatic compounds. Commonly employed in the development of active pharmaceutical ingredients (APIs) where ester and aryl iodide functionalities are required. Also utilized in research laboratories for the synthesis of liquid crystals and functional materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 2g
10-20 days ฿162.00
inventory 10g
10-20 days ฿320.00
inventory 50g
10-20 days ฿1,150.00
inventory 250g
10-20 days ฿5,560.00
inventory 1kg
10-20 days ฿21,630.00
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Ethyl 4-Iodobenzoate
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Used as an intermediate in organic synthesis, particularly 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 allows for selective functionalization, making it valuable in the preparation of complex aromatic compounds. Commonly employed in the development of active pharmaceutical ingredients (APIs) where ester and aryl iodide functionalities are required.

Used as an intermediate in organic synthesis, particularly 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 allows for selective functionalization, making it valuable in the preparation of complex aromatic compounds. Commonly employed in the development of active pharmaceutical ingredients (APIs) where ester and aryl iodide functionalities are required. Also utilized in research laboratories for the synthesis of liquid crystals and functional materials.

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