(3-Oxo-2,3-dihydro-1H-inden-5-yl)boronic acid
95%
Reagent
Code: #220951
CAS Number
1135871-83-8
science Other reagents with same CAS 1135871-83-8
blur_circular Chemical Specifications
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Molecular Information
Weight
175.98 g/mol
Formula
C₉H₉BO₃
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Registry Numbers
MDL Number
MFCD22191954
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Physical Properties
Boiling Point
396.2±52.0 °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 in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid functionality allows for efficient coupling with aryl halides, making it valuable in constructing biaryl systems found in bioactive molecules. Commonly employed in the synthesis of indanone derivatives, which are structural motifs in medicinal chemistry for drug discovery targeting inflammation, cancer, and central nervous system disorders. Also utilized in materials science for creating conjugated organic frameworks with potential applications in optoelectronics.
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