2-Iodophenyl acetate

98%

Reagent Code: #200454
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CAS Number 32865-61-5

science Other reagents with same CAS 32865-61-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.04 g/mol
Formula C₈H₇IO₂
badge Registry Numbers
MDL Number MFCD07780625
thermostat Physical Properties
Boiling Point 273°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed, light-proof

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the preparation of indoles and other heterocyclic compounds through palladium-catalyzed or copper-mediated cyclization reactions. It serves as a versatile building block in pharmaceutical and agrochemical research due to the reactivity of the iodine atom, which allows for cross-coupling reactions such as Suzuki or Heck couplings. Its acetate group can also be hydrolyzed or transformed, enabling further functionalization. Commonly employed in the development of bioactive molecules and complex polycyclic structures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿560.00
inventory 5g
10-20 days ฿2,760.00
inventory 25g
10-20 days ฿13,760.00
2-Iodophenyl acetate
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Used primarily as an intermediate in organic synthesis, particularly in the preparation of indoles and other heterocyclic compounds through palladium-catalyzed or copper-mediated cyclization reactions. It serves as a versatile building block in pharmaceutical and agrochemical research due to the reactivity of the iodine atom, which allows for cross-coupling reactions such as Suzuki or Heck couplings. Its acetate group can also be hydrolyzed or transformed, enabling further functionalization. Commonly emp

Used primarily as an intermediate in organic synthesis, particularly in the preparation of indoles and other heterocyclic compounds through palladium-catalyzed or copper-mediated cyclization reactions. It serves as a versatile building block in pharmaceutical and agrochemical research due to the reactivity of the iodine atom, which allows for cross-coupling reactions such as Suzuki or Heck couplings. Its acetate group can also be hydrolyzed or transformed, enabling further functionalization. Commonly employed in the development of bioactive molecules and complex polycyclic structures.

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