7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]isothiazole

97%

Reagent Code: #238160
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CAS Number 1326713-92-1

science Other reagents with same CAS 1326713-92-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.15 g/mol
Formula C₁₃H₁₆BNO₂S
thermostat Physical Properties
Boiling Point 326.6±24.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a key 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 heteroaryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the benzoisothiazole moiety into target structures, which is a common scaffold in bioactive compounds and functional materials. Its stability and reactivity profile make it suitable for late-stage functionalization in drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,350.00
inventory 1g
10-20 days ฿75,010.00
7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]isothiazole
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Used primarily as a key 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 heteroaryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the benzoisothiazole moiety into target structures, which is a common scaffold in bioactive compounds and

Used primarily as a key 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 heteroaryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for introducing the benzoisothiazole moiety into target structures, which is a common scaffold in bioactive compounds and functional materials. Its stability and reactivity profile make it suitable for late-stage functionalization in drug discovery and development.

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