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

95%

Reagent Code: #90757
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CAS Number 2223032-96-8

science Other reagents with same CAS 2223032-96-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.17756 g/mol
Formula C₁₃H₁₉BN₂O₃S
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 the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of active pharmaceutical ingredients (APIs) and other fine chemicals. Additionally, its pyrazole moiety contributes to its use in designing compounds with potential biological activity, such as enzyme inhibitors or receptor modulators. Its stability and reactivity make it a versatile reagent in medicinal chemistry and material science research.

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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-Pyrazol-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 the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of active pharmaceutical ingredients (APIs) and other fine chemicals. A

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of active pharmaceutical ingredients (APIs) and other fine chemicals. Additionally, its pyrazole moiety contributes to its use in designing compounds with potential biological activity, such as enzyme inhibitors or receptor modulators. Its stability and reactivity make it a versatile reagent in medicinal chemistry and material science research.

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