(2,6-Dibromophenyl)boronic acid

95%

Reagent Code: #88989
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CAS Number 851756-50-8

science Other reagents with same CAS 851756-50-8

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scatter_plot Molecular Information
Weight 279.7217 g/mol
Formula C₆H₅BBr₂O₂
badge Registry Numbers
MDL Number MFCD11656174
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. These compounds are valuable in pharmaceuticals, agrochemicals, and materials science. Acts as a key intermediate in the development of active pharmaceutical ingredients (APIs) and fine chemicals. Its boronic acid group enables efficient coupling with aryl halides, making it a versatile reagent in medicinal chemistry for drug discovery and development. Also employed in the synthesis of advanced materials, such as organic light-emitting diodes (OLEDs) and liquid crystals, due to its ability to form stable carbon-carbon bonds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,926.00
inventory 250mg
10-20 days ฿2,880.00
inventory 1g
10-20 days ฿7,182.00
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(2,6-Dibromophenyl)boronic acid
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Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. These compounds are valuable in pharmaceuticals, agrochemicals, and materials science. Acts as a key intermediate in the development of active pharmaceutical ingredients (APIs) and fine chemicals. Its boronic acid group enables efficient coupling with aryl halides, making it a versatile reagent in medicinal chemistry for drug discovery and development. Also employed in the s

Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. These compounds are valuable in pharmaceuticals, agrochemicals, and materials science. Acts as a key intermediate in the development of active pharmaceutical ingredients (APIs) and fine chemicals. Its boronic acid group enables efficient coupling with aryl halides, making it a versatile reagent in medicinal chemistry for drug discovery and development. Also employed in the synthesis of advanced materials, such as organic light-emitting diodes (OLEDs) and liquid crystals, due to its ability to form stable carbon-carbon bonds.

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