(6-phenyldibenzo[b,d]furan-4-yl)boronic acid

≥98%

Reagent Code: #90973
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CAS Number 1010068-85-5

science Other reagents with same CAS 1010068-85-5

blur_circular Chemical Specifications

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Weight 288.11 g/mol
Formula C₁₈H₁₃BO₃
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl structures. These structures are valuable in pharmaceuticals, agrochemicals, and materials science. Acts as a key intermediate in the development of organic electronic materials, such as OLEDs and semiconductors, due to its ability to form stable conjugated systems. Also employed in the preparation of polymers and advanced materials with specific optical and electronic properties. Its boronic acid group enables efficient and selective coupling with various aryl halides, making it a versatile building block in synthetic chemistry.

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inventory 1g
10-20 days ฿5,710.00

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(6-phenyldibenzo[b,d]furan-4-yl)boronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl structures. These structures are valuable in pharmaceuticals, agrochemicals, and materials science. Acts as a key intermediate in the development of organic electronic materials, such as OLEDs and semiconductors, due to its ability to form stable conjugated systems. Also employed in the preparation of polymers and advanced materials with specific optical and electronic properties. Its boronic acid

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl structures. These structures are valuable in pharmaceuticals, agrochemicals, and materials science. Acts as a key intermediate in the development of organic electronic materials, such as OLEDs and semiconductors, due to its ability to form stable conjugated systems. Also employed in the preparation of polymers and advanced materials with specific optical and electronic properties. Its boronic acid group enables efficient and selective coupling with various aryl halides, making it a versatile building block in synthetic chemistry.

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