(5-(Pyrrolidin-1-yl)pyridin-3-yl)boronic acid

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Reagent Code: #226373
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CAS Number 1218790-56-7

science Other reagents with same CAS 1218790-56-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.02 g/mol
Formula C₉H₁₃BN₂O₂
badge Registry Numbers
MDL Number MFCD15143459
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical research. Its boronic acid functionality enables efficient carbon-carbon bond formation with aryl halides, making it valuable in constructing complex pyridine-based structures. Commonly applied in the development of drug candidates targeting central nervous system disorders and inflammatory diseases due to the enhanced pharmacokinetic properties imparted by the pyrrolidinyl-pyridine scaffold. Also employed in the preparation of ligands for catalysis and in the design of functional materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,320.00
250mg
10-20 days ฿6,650.00
(5-(Pyrrolidin-1-yl)pyridin-3-yl)boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical research. Its boronic acid functionality enables efficient carbon-carbon bond formation with aryl halides, making it valuable in constructing complex pyridine-based structures. Commonly applied in the development of drug candidates targeting central nervous system disorders and inflammatory diseases due to the enhanced pharmacokinetic properties imparted

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active compounds, particularly in pharmaceutical research. Its boronic acid functionality enables efficient carbon-carbon bond formation with aryl halides, making it valuable in constructing complex pyridine-based structures. Commonly applied in the development of drug candidates targeting central nervous system disorders and inflammatory diseases due to the enhanced pharmacokinetic properties imparted by the pyrrolidinyl-pyridine scaffold. Also employed in the preparation of ligands for catalysis and in the design of functional materials.

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