3-(Pyrrolidino)phenylboronic acid

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Reagent Code: #117483
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CAS Number 659731-18-7

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.04 g/mol
Formula C₁₀H₁₄BNO₂
badge Registry Numbers
MDL Number MFCD03095125
thermostat Physical Properties
Boiling Point 403.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used in organic synthesis as a key intermediate for constructing complex molecules, particularly in Suzuki-Miyaura cross-coupling reactions, which are vital for creating pharmaceuticals and agrochemicals. Acts as a ligand in catalysis, enhancing reaction efficiency and selectivity. Applied in materials science for developing organic electronic devices due to its boronic acid group, which facilitates binding to diols and other functional groups. Also utilized in biochemical research for probing and modifying biomolecules, aiding in the study of cellular processes and drug discovery. Its unique structure enables applications in sensor development for detecting sugars and other analytes.

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Test Parameter Specification
APPEARANCE Off-white to gray Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿13,970.00
inventory 100mg
10-20 days ฿1,230.00
inventory 250mg
10-20 days ฿2,060.00
inventory 1g
10-20 days ฿4,170.00

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3-(Pyrrolidino)phenylboronic acid
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Used in organic synthesis as a key intermediate for constructing complex molecules, particularly in Suzuki-Miyaura cross-coupling reactions, which are vital for creating pharmaceuticals and agrochemicals. Acts as a ligand in catalysis, enhancing reaction efficiency and selectivity. Applied in materials science for developing organic electronic devices due to its boronic acid group, which facilitates binding to diols and other functional groups. Also utilized in biochemical research for probing and modify

Used in organic synthesis as a key intermediate for constructing complex molecules, particularly in Suzuki-Miyaura cross-coupling reactions, which are vital for creating pharmaceuticals and agrochemicals. Acts as a ligand in catalysis, enhancing reaction efficiency and selectivity. Applied in materials science for developing organic electronic devices due to its boronic acid group, which facilitates binding to diols and other functional groups. Also utilized in biochemical research for probing and modifying biomolecules, aiding in the study of cellular processes and drug discovery. Its unique structure enables applications in sensor development for detecting sugars and other analytes.

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