Bis(4-bromophenylboronic Acid) scyllo-Inositol Complex Dipotassium Tetrahydrate

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Reagent Code: #91105
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CAS Number 1537876-29-1

science Other reagents with same CAS 1537876-29-1

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Weight 585.93(as Anhydrous) g/mol
Formula C₁₈H₁₄B₂Br₂K₂O₆₄H₂O
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This complex is primarily utilized in organic synthesis and pharmaceutical research due to its unique boronic acid and inositol structure. It serves as a key intermediate in the development of boron-containing compounds, which are essential in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. Its application extends to the synthesis of biologically active molecules, including potential drug candidates, particularly in targeting diseases like cancer and diabetes. The compound’s stability and solubility in aqueous solutions make it suitable for use in biochemical studies and as a building block for complex organic frameworks. Additionally, it is explored in materials science for designing advanced polymers and sensors.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿2,097.00

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Bis(4-bromophenylboronic Acid) scyllo-Inositol Complex Dipotassium Tetrahydrate
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This complex is primarily utilized in organic synthesis and pharmaceutical research due to its unique boronic acid and inositol structure. It serves as a key intermediate in the development of boron-containing compounds, which are essential in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. Its application extends to the synthesis of biologically active molecules, including potential drug candidates, particularly in targeting diseases like cancer and diabete

This complex is primarily utilized in organic synthesis and pharmaceutical research due to its unique boronic acid and inositol structure. It serves as a key intermediate in the development of boron-containing compounds, which are essential in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. Its application extends to the synthesis of biologically active molecules, including potential drug candidates, particularly in targeting diseases like cancer and diabetes. The compound’s stability and solubility in aqueous solutions make it suitable for use in biochemical studies and as a building block for complex organic frameworks. Additionally, it is explored in materials science for designing advanced polymers and sensors.

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