6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)chroman-2-one

95%

Reagent Code: #130658
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CAS Number 2484920-14-9

science Other reagents with same CAS 2484920-14-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.12 g/mol
Formula C₁₅H₁₉BO₄
badge Registry Numbers
MDL Number MFCD28385796
thermostat Physical Properties
Boiling Point 412.1±34.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.15±0.1 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used primarily as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for constructing biologically active chromanone derivatives, which are found in natural products and drug candidates with antioxidant, anti-inflammatory, or anticancer properties. The compound’s stability and reactivity profile make it suitable for late-stage functionalization in medicinal chemistry campaigns.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,090.00
inventory 250mg
10-20 days ฿8,640.00
inventory 1g
10-20 days ฿23,340.00

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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)chroman-2-one
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Used primarily as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for constructing biologically active chromanone derivatives, which are found in natural products and drug candidates with antioxi

Used primarily as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for constructing biologically active chromanone derivatives, which are found in natural products and drug candidates with antioxidant, anti-inflammatory, or anticancer properties. The compound’s stability and reactivity profile make it suitable for late-stage functionalization in medicinal chemistry campaigns.

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