[1,1'-bi(cyclopropan)]-2-ylboronic acid

95%

Reagent Code: #91032
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CAS Number 1643878-69-6

science Other reagents with same CAS 1643878-69-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 125.96134 g/mol
Formula C₆H₁₁BO₂
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key reagent for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its cyclopropane rings contribute to unique steric and electronic properties, making it valuable in the synthesis of pharmaceuticals and agrochemicals. Additionally, it is employed in the development of advanced materials, including polymers and liquid crystals, due to its ability to introduce cyclopropane moieties into target structures. Its boronic acid group also allows for further functionalization, enhancing its versatility in chemical transformations.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿78,000.00
inventory 100mg
10-20 days ฿230,000.00

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[1,1'-bi(cyclopropan)]-2-ylboronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key reagent for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its cyclopropane rings contribute to unique steric and electronic properties, making it valuable in the synthesis of pharmaceuticals and agrochemicals. Additionally, it is employed in the development of advanced materials, including polymers and liquid

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key reagent for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its cyclopropane rings contribute to unique steric and electronic properties, making it valuable in the synthesis of pharmaceuticals and agrochemicals. Additionally, it is employed in the development of advanced materials, including polymers and liquid crystals, due to its ability to introduce cyclopropane moieties into target structures. Its boronic acid group also allows for further functionalization, enhancing its versatility in chemical transformations.

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