5-(1H-Pyrrol-1-yl)furan-2-boronic acid pinacol ester

95%

Reagent Code: #90756
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CAS Number 2223031-84-1

science Other reagents with same CAS 2223031-84-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.1239 g/mol
Formula C₁₄H₂₀BNO₄
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a crucial building block for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of drug candidates, where precise molecular architectures are required. Additionally, it finds applications in material science for synthesizing advanced polymers and organic electronic materials, contributing to innovations in flexible electronics and optoelectronics.

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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-(1H-Pyrrol-1-yl)furan-2-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a crucial building block for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of drug candidates, where precise molecular architectures are required.

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a crucial building block for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of drug candidates, where precise molecular architectures are required. Additionally, it finds applications in material science for synthesizing advanced polymers and organic electronic materials, contributing to innovations in flexible electronics and optoelectronics.

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