7-Phenyldibenzo[b,d]furan-1-yltrifluoromethanesulfonate

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Reagent Code: #227904
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CAS Number 2128707-95-7

science Other reagents with same CAS 2128707-95-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 392.35 g/mol
Formula C₁₉H₁₁F₃O₄S
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. Its triflate group acts as a highly reactive leaving group, enabling efficient carbon-carbon bond formation. This makes it valuable in the preparation of complex organic molecules, including conjugated materials used in organic semiconductors, OLEDs, and pharmaceuticals. The presence of the dibenzofuran core contributes to thermal stability and electronic properties beneficial in optoelectronic applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,280.00
inventory 250mg
10-20 days ฿3,950.00
inventory 1g
10-20 days ฿11,990.00

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7-Phenyldibenzo[b,d]furan-1-yltrifluoromethanesulfonate
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Used as a key intermediate in organic synthesis, particularly in palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. Its triflate group acts as a highly reactive leaving group, enabling efficient carbon-carbon bond formation. This makes it valuable in the preparation of complex organic molecules, including conjugated materials used in organic semiconductors, OLEDs, and pharmaceuticals. The presence of the dibenzofuran core contributes to thermal stability and electroni

Used as a key intermediate in organic synthesis, particularly in palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. Its triflate group acts as a highly reactive leaving group, enabling efficient carbon-carbon bond formation. This makes it valuable in the preparation of complex organic molecules, including conjugated materials used in organic semiconductors, OLEDs, and pharmaceuticals. The presence of the dibenzofuran core contributes to thermal stability and electronic properties beneficial in optoelectronic applications.

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