Cyclopropylboronic acid pinacol ester

96%

Reagent Code: #91172
label
Alias Cyclopropyl borate pinacol ester 2-Cyclopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 2-cyclopropyl-4,4,5,5-tetramethyl-1,3,2-dioxaborane
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CAS Number 126689-01-8

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.04 g/mol
Formula C₉H₁₇BO₂
badge Registry Numbers
MDL Number MFCD05663847
thermostat Physical Properties
Boiling Point 146 °C
inventory_2 Storage & Handling
Density 0.922 g/mL at 25 °C
Storage 2~8°C

description Product Description

Cyclopropylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for introducing the cyclopropyl group into various organic molecules, enabling the construction of complex structures. This compound is valuable in pharmaceutical research for synthesizing drug candidates, especially those requiring cyclopropane rings for biological activity. It is also employed in material science for designing advanced polymers and functional materials. Its stability and reactivity make it a preferred choice in catalytic processes, facilitating efficient and selective transformations in synthetic chemistry.

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Test Parameter Specification
Purity (GC) 96-100
Purity (Titration by NaOH) 95.5-101.5
Refractive Index n20D 1.433-1.437
Specific Gravity (20°C) 0.929-0.933
Appearance colorless to brown liquid
Boron NMR Spectra Conforms to Structure
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿1,120.00
inventory 25g
10-20 days ฿3,730.00

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Cyclopropylboronic acid pinacol ester
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Cyclopropylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for introducing the cyclopropyl group into various organic molecules, enabling the construction of complex structures. This compound is valuable in pharmaceutical research for synthesizing drug candidates, especially those requiring cyclopropane rings for biological activity. It is also employed in material science for designing advanced polymers a

Cyclopropylboronic acid pinacol ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for introducing the cyclopropyl group into various organic molecules, enabling the construction of complex structures. This compound is valuable in pharmaceutical research for synthesizing drug candidates, especially those requiring cyclopropane rings for biological activity. It is also employed in material science for designing advanced polymers and functional materials. Its stability and reactivity make it a preferred choice in catalytic processes, facilitating efficient and selective transformations in synthetic chemistry.

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