8-Quinolinylboronic acid

97%

Reagent Code: #90976
label
Alias Quinoline-8-boronic acid
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CAS Number 86-58-8

science Other reagents with same CAS 86-58-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.98 g/mol
Formula C₉H₈BNO₂
badge Registry Numbers
MDL Number MFCD01114698
thermostat Physical Properties
Melting Point >300 °C(lit.)
Boiling Point 160-165°C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. It also serves as a building block in the development of fluorescent probes and sensors for detecting metal ions or biomolecules. Additionally, it finds application in material science for designing organic electronic devices and polymers. Its boronic acid group enables it to form stable complexes with diols, making it useful in carbohydrate recognition and separation processes.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (HPLC) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Spectrum Conforms to Structure
Appearance White to Tan Powder, Crystals, Crystalline Powder and/or Chunks

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿390.00
inventory 1g
10-20 days ฿760.00

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8-Quinolinylboronic acid
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Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. It also serves as a building block in the development of fluorescent probes and sensors for detecting metal ions or biomolecules. Additionally, it finds application in material science for designing organic electronic devices and polymers. Its boronic acid group enables it to form stable complexes with diols, making

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. It also serves as a building block in the development of fluorescent probes and sensors for detecting metal ions or biomolecules. Additionally, it finds application in material science for designing organic electronic devices and polymers. Its boronic acid group enables it to form stable complexes with diols, making it useful in carbohydrate recognition and separation processes.

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