(2-Hydroxynaphthalen-1-yl)boronic acid
95%
Reagent
Code: #131609
CAS Number
898257-48-2
blur_circular Chemical Specifications
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Molecular Information
Weight
187.99 g/mol
Formula
C₁₀H₉BO₃
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Registry Numbers
MDL Number
MFCD09751353
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Physical Properties
Boiling Point
434.2±47.0 °C(Predicted)
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Storage & Handling
Density
1.35±0.1 g/cm3(Predicted)
Storage
2-8°C, Sealed, Inert Gas
description Product Description
Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct biaryl compounds. Its hydroxyl group enhances solubility and can act as a directing group or coordination site in metal-catalyzed reactions. Commonly employed in the development of pharmaceuticals, agrochemicals, and functional materials such as organic semiconductors and sensors. The compound's ability to form stable complexes with diols makes it useful in saccharide sensing applications. Also explored in the synthesis of fluorescent probes and dyes due to the naphthalene backbone’s inherent photophysical properties.
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