(1-Oxo-2,3-dihydro-1H-inden-5-yl)boronic acid
98%
Reagent
Code: #220955
CAS Number
221006-64-0
blur_circular Chemical Specifications
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Molecular Information
Weight
175.97 g/mol
Formula
C₉H₉BO₃
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Registry Numbers
MDL Number
MFCD22414434
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Physical Properties
Boiling Point
410.2±55.0 °C(Predicted)
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Storage & Handling
Density
1.31±0.1 g/cm3(Predicted)
Storage
2-8°C, 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 boronic acid functionality allows for efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research for developing complex aromatic structures. The indanone-derived scaffold contributes to enhanced stability and reactivity in coupling processes. Commonly employed in the synthesis of bioactive molecules and functional materials where substituted indanone motifs are required.
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