2-Methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

97%

Reagent Code: #130986
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CAS Number 1437769-82-8

science Other reagents with same CAS 1437769-82-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.1 g/mol
Formula C₁₃H₁₉BO₄
badge Registry Numbers
MDL Number MFCD16994340
thermostat Physical Properties
Boiling Point 355.1±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.11±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required. Stable and compatible with a wide range of functional groups, making it valuable in late-stage functionalization during drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,450.00
inventory 1g
10-20 days ฿12,000.00

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2-Methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required. Stable and compatible with a wide range of functional groups, making it valuable in late-stag

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required. Stable and compatible with a wide range of functional groups, making it valuable in late-stage functionalization during drug discovery.

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