(3-(nicotinamido)phenyl)boronic acid

95%

Reagent Code: #218349
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CAS Number 109445-19-4

science Other reagents with same CAS 109445-19-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.03834 g/mol
Formula C₁₂H₁₁BN₂O₃
badge Registry Numbers
MDL Number MFCD22571909
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as a building block for pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in creating biaryl structures found in drug candidates. Also applied in the synthesis of fluorescent probes and sensors due to its ability to interact with diols and participate in selective binding reactions. Its nicotinamide moiety supports interactions in biological systems, enhancing utility in medicinal chemistry research.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿7,200.00
1g
10-20 days ฿16,000.00
(3-(nicotinamido)phenyl)boronic acid
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Used in organic synthesis as a building block for pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in creating biaryl structures found in drug candidates. Also applied in the synthesis of fluorescent probes and sensors due to its ability to interact with diols and participate in selective binding reactions. Its nicotinamide moiety supports interactions in biologic

Used in organic synthesis as a building block for pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its boronic acid group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in creating biaryl structures found in drug candidates. Also applied in the synthesis of fluorescent probes and sensors due to its ability to interact with diols and participate in selective binding reactions. Its nicotinamide moiety supports interactions in biological systems, enhancing utility in medicinal chemistry research.

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