(4-(9-Phenyl-9H-Carbazol-3-yl)Phenyl)Boronic Acid

≥98%

Reagent Code: #89250
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CAS Number 1240963-55-6

science Other reagents with same CAS 1240963-55-6

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Weight 363.22 g/mol
Formula C₂₄H₁₈BNO₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating carbon-carbon bonds. Additionally, it finds application in the synthesis of organic electronic materials, such as OLEDs, due to its carbazole moiety, which contributes to charge transport properties. Its role in medicinal chemistry includes the development of bioactive compounds and drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿711.00
inventory 1g
10-20 days ฿1,917.00
inventory 5g
10-20 days ฿6,705.00
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(4-(9-Phenyl-9H-Carbazol-3-yl)Phenyl)Boronic Acid
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating carbon-carbon bonds. Additionally, it finds application in the synthesis of organic electronic materials, such as OLEDs, due to its carbazole moiety,

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in creating carbon-carbon bonds. Additionally, it finds application in the synthesis of organic electronic materials, such as OLEDs, due to its carbazole moiety, which contributes to charge transport properties. Its role in medicinal chemistry includes the development of bioactive compounds and drug candidates.

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