Tert-butyl 5,6-dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-1(2H)-carboxylate

≥95%

Reagent Code: #91028
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CAS Number 286961-14-6

science Other reagents with same CAS 286961-14-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.21 g/mol
Formula C₁₆H₂₈BNO₄
badge Registry Numbers
MDL Number MFCD03840345
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a valuable boron-containing intermediate, enabling the formation of carbon-carbon bonds in the construction of complex molecules. Its stability and reactivity make it suitable for use in pharmaceutical research and development, where it aids in the synthesis of biologically active compounds. Additionally, it is employed in materials science for the preparation of advanced organic materials, including polymers and ligands for catalysis. Its tert-butyloxycarbonyl (Boc) protecting group ensures selective reactivity, making it a versatile tool in synthetic chemistry.

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Test Parameter Specification
Purity (HPLC) 95-100%
Water 0-0.5%
Appearance White to off-white solid

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿420.00
inventory 5g
10-20 days ฿1,460.00
inventory 25g
10-20 days ฿4,600.00

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Tert-butyl 5,6-dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-1(2H)-carboxylate
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a valuable boron-containing intermediate, enabling the formation of carbon-carbon bonds in the construction of complex molecules. Its stability and reactivity make it suitable for use in pharmaceutical research and development, where it aids in the synthesis of biologically active compounds. Additionally, it is employed in materials science for the preparation o

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a valuable boron-containing intermediate, enabling the formation of carbon-carbon bonds in the construction of complex molecules. Its stability and reactivity make it suitable for use in pharmaceutical research and development, where it aids in the synthesis of biologically active compounds. Additionally, it is employed in materials science for the preparation of advanced organic materials, including polymers and ligands for catalysis. Its tert-butyloxycarbonyl (Boc) protecting group ensures selective reactivity, making it a versatile tool in synthetic chemistry.

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