5-(2-Methylpiperidin-1-yl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90767
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CAS Number 2223003-34-5

science Other reagents with same CAS 2223003-34-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.27442 g/mol
Formula C₁₆H₂₈BNO₃S
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 intermediate in the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic ester functionality allows for efficient and selective bond formation, making it valuable in constructing carbon-carbon bonds. Additionally, it is employed in the development of advanced materials and in research for creating novel compounds with potential biological activity. Its stability and reactivity make it a preferred choice in medicinal chemistry for drug discovery and development.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿15,552.00
inventory 100mg
10-20 days ฿46,602.00

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5-(2-Methylpiperidin-1-yl)thiophene-2-boronic acid pinacol ester
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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 intermediate in the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic ester functionality allows for efficient and selective bond formation, making it valuable in constructing carbon-carbon bonds. Additionally, it is employed in the development of advanced materials and in research for creating novel compoun

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic ester functionality allows for efficient and selective bond formation, making it valuable in constructing carbon-carbon bonds. Additionally, it is employed in the development of advanced materials and in research for creating novel compounds with potential biological activity. Its stability and reactivity make it a preferred choice in medicinal chemistry for drug discovery and development.

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