Cyclopropylboronic acid pinacol ester

96%

  • Product Code: 91172
  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
  CAS:    126689-01-8
Molecular Weight: 168.04 g./mol Molecular Formula: C₉H₁₇BO₂
EC Number: MDL Number: MFCD05663847
Melting Point: Boiling Point: 146 °C
Density: 0.922 g/mL at 25 °C Storage Condition: 2~8°C
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.
Product Specification:
Test Specification
PurityGC 96-100
PURITYTITRATION BY NAOH 95.5-101.5
REFRACTIVE INDEX N20D 1.433-1.437
SPECIFIC GRAVITY 2020C 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
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿300.00
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-
5.000 10-20 days ฿1,120.00
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-
25.000 10-20 days ฿3,730.00
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Cyclopropylboronic acid pinacol ester
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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