4-Bromodibenzo[b,d]furan-1-yltrifluoromethanesulfonate

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Reagent Code: #155349
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CAS Number 2247123-54-0

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 395.15 g/mol
Formula C₁₃H₆BrF₃O₄S
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki and Stille couplings, enabling the formation of complex dibenzofuran derivatives. These derivatives are valuable in the development of organic electronic materials, including semiconductors and light-emitting compounds used in OLEDs. Also employed in pharmaceutical research for constructing biaryl frameworks with specific electronic or steric properties. Its triflate group enhances reactivity toward palladium-catalyzed transformations, making it a versatile building block in synthetic chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,560.00
250mg
10-20 days ฿7,590.00
1g
10-20 days ฿15,170.00
5g
10-20 days ฿55,850.00
4-Bromodibenzo[b,d]furan-1-yltrifluoromethanesulfonate
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Used as an intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki and Stille couplings, enabling the formation of complex dibenzofuran derivatives. These derivatives are valuable in the development of organic electronic materials, including semiconductors and light-emitting compounds used in OLEDs. Also employed in pharmaceutical research for constructing biaryl frameworks with specific electronic or steric properties. Its triflate group enhances reactivity toward pall

Used as an intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki and Stille couplings, enabling the formation of complex dibenzofuran derivatives. These derivatives are valuable in the development of organic electronic materials, including semiconductors and light-emitting compounds used in OLEDs. Also employed in pharmaceutical research for constructing biaryl frameworks with specific electronic or steric properties. Its triflate group enhances reactivity toward palladium-catalyzed transformations, making it a versatile building block in synthetic chemistry.

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