2-[4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethan-1-ol

95%

Reagent Code: #243116
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CAS Number 741699-47-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.129 g/mol
Formula C₁₄H₂₁BO₄
thermostat Physical Properties
Boiling Point 391.2±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.09±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its phenolic ether structure with a terminal hydroxyl group allows for selective modifications and functionalization, making it valuable in the preparation of pharmaceutical intermediates, liquid crystals, and conjugated organic materials. The presence of the dioxaborolane ring enhances stability and reactivity under palladium catalysis, while the hydroxyl group enables further derivatization, such as esterification or ether formation, for use in polymer chemistry or prodrug design.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,190.00
inventory 1g
10-20 days ฿5,260.00
inventory 5g
10-20 days ฿19,620.00
2-[4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethan-1-ol
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its phenolic ether structure with a terminal hydroxyl group allows for selective modifications and functionalization, making it valuable in the preparation of pharmaceutical intermediates, liquid crystals, and conjugated organic materials. The presence of the dioxaborolane ring enhances stability and reactivity under palladium catalysis, while the hydroxyl group enables further derivatization, such as esterification or ether formation, for use in polymer chemistry or prodrug design.
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