2-(3-Chloro-4-isopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

98%

Reagent Code: #130761
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CAS Number 1260023-79-7

science Other reagents with same CAS 1260023-79-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.6 g/mol
Formula C₁₅H₂₂BClO₃
badge Registry Numbers
MDL Number MFCD18384181
thermostat Physical Properties
Boiling Point 376.7±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.09±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides under mild conditions, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the isopropoxy and chloro substituents allows for further functionalization or serves as a directing group in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,850.00
inventory 5g
10-20 days ฿33,550.00
inventory 1g
10-20 days ฿7,720.00

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2-(3-Chloro-4-isopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides under mild conditions, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the isopropoxy and chloro substituents allows for further functionalization or serves as a dire

Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl or vinyl halides under mild conditions, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the isopropoxy and chloro substituents allows for further functionalization or serves as a directing group in synthetic pathways.

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