4-(Trifluoromethoxy)iodobenzene

98%

Reagent Code: #239893
label
Alias 1-Iodine-4 (trifluoromethoxy)benzene; p-iodine trifluoromethoxybenzene, 4-iodine trifluoromethoxybenzene
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CAS Number 103962-05-6

science Other reagents with same CAS 103962-05-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.01 g/mol
Formula C₇H₄F₃IO
badge Registry Numbers
MDL Number MFCD00042411
thermostat Physical Properties
Boiling Point 177-179 °C(lit.)
inventory_2 Storage & Handling
Density 1.84 g/mL at 25 °C(lit.)
Storage 2~8°C, avoiding light

description Product Description

Widely used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions, enabling the construction of complex aromatic compounds. Its iodine functionality acts as a reactive site for palladium-catalyzed transformations, making it valuable in pharmaceutical and agrochemical research. The trifluoromethoxy group enhances lipophilicity and metabolic stability, which is beneficial in drug design for improving bioavailability and resistance to degradation. Commonly employed as a building block in the development of bioactive molecules and functional materials.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿290.00
inventory 5g
10-20 days ฿330.00
inventory 25g
10-20 days ฿690.00
inventory 100g
10-20 days ฿2,450.00

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4-(Trifluoromethoxy)iodobenzene
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Widely used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions, enabling the construction of complex aromatic compounds. Its iodine functionality acts as a reactive site for palladium-catalyzed transformations, making it valuable in pharmaceutical and agrochemical research. The trifluoromethoxy group enhances lipophilicity and metabolic stability, which is beneficial in drug design for improving bioavailability and resistance to degradation. Commonly

Widely used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions, enabling the construction of complex aromatic compounds. Its iodine functionality acts as a reactive site for palladium-catalyzed transformations, making it valuable in pharmaceutical and agrochemical research. The trifluoromethoxy group enhances lipophilicity and metabolic stability, which is beneficial in drug design for improving bioavailability and resistance to degradation. Commonly employed as a building block in the development of bioactive molecules and functional materials.

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