(4-Formyl-2-methoxyphenyl)boronic acid

97%

Reagent Code: #90705
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CAS Number 1028479-47-1

science Other reagents with same CAS 1028479-47-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.97 g/mol
Formula C₈H₉BO₄
thermostat Physical Properties
Melting Point 152-155°C
Boiling Point 400.7±55.0°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used primarily in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and biologically active compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Its boronic acid group enables efficient coupling with aryl halides, making it a versatile building block for drug discovery and development. Additionally, it finds applications in the synthesis of materials for organic electronics and sensors due to its ability to form stable complexes with diols and other functional groups.

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Test Parameter Specification
Appearance White to yellow 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 250mg
10-20 days ฿670.00
inventory 1g
10-20 days ฿2,480.00
inventory 5g
10-20 days ฿11,890.00

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(4-Formyl-2-methoxyphenyl)boronic acid
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Used primarily in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and biologically active compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Its boronic acid group enables efficient coupling with aryl halides, making it a versatile building block for drug discovery and development. Additionally, it finds applications in the synthesis o

Used primarily in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and biologically active compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Its boronic acid group enables efficient coupling with aryl halides, making it a versatile building block for drug discovery and development. Additionally, it finds applications in the synthesis of materials for organic electronics and sensors due to its ability to form stable complexes with diols and other functional groups.

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