Ethyl 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopropanecarboxylate

95%

Reagent Code: #115702
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CAS Number 1215107-29-1

science Other reagents with same CAS 1215107-29-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.10 g/mol
Formula C₁₂H₂₁BO₄
badge Registry Numbers
MDL Number MFCD24449649
thermostat Physical Properties
Boiling Point 266.7±33.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily used in organic synthesis as a key intermediate in cross-coupling reactions, particularly Suzuki-Miyaura coupling. It facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its cyclopropane and boronate ester functionalities enhance its reactivity and selectivity in these transformations. Additionally, it is employed in the development of novel materials and bioactive compounds, contributing to advancements in medicinal chemistry and material science.

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Test Parameter Specification
Appearance Colorless Liquid
Purity (%) 94.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿12,240.00
inventory 100mg
10-20 days ฿3,186.00
inventory 250mg
10-20 days ฿4,860.00

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Ethyl 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopropanecarboxylate
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This compound is primarily used in organic synthesis as a key intermediate in cross-coupling reactions, particularly Suzuki-Miyaura coupling. It facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its cyclopropane and boronate ester functionalities enhance its reactivity and selectivity in these transformations. Additionally, it is employed in the development of novel materials and bioactive compo

This compound is primarily used in organic synthesis as a key intermediate in cross-coupling reactions, particularly Suzuki-Miyaura coupling. It facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its cyclopropane and boronate ester functionalities enhance its reactivity and selectivity in these transformations. Additionally, it is employed in the development of novel materials and bioactive compounds, contributing to advancements in medicinal chemistry and material science.

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