(3-Oxo-2,3-dihydro-1H-inden-5-yl)boronic acid

95%

Reagent Code: #220951
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CAS Number 1135871-83-8

science Other reagents with same CAS 1135871-83-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.98 g/mol
Formula C₉H₉BO₃
badge Registry Numbers
MDL Number MFCD22191954
thermostat Physical Properties
Boiling Point 396.2±52.0 °C(Predicted)
inventory_2 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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿14,700.00
1g
10-20 days ฿64,990.00
(3-Oxo-2,3-dihydro-1H-inden-5-yl)boronic acid
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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
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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