5-(4-Methoxyphenyl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90803
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CAS Number 1402227-48-8

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blur_circular Chemical Specifications

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Weight 334.23812 g/mol
Formula C₁₇H₂₃BO₄S
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 development of pharmaceuticals, agrochemicals, and organic materials. 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 synthesis of biologically active compounds, including potential drug candidates. Additionally, it finds use in the preparation of conjugated polymers and organic electronic materials, contributing to advancements in optoelectronics and photovoltaics. Its stability and reactivity make it a versatile tool in modern synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,982.00
inventory 25mg
10-20 days ฿19,800.00

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5-(4-Methoxyphenyl)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 development of pharmaceuticals, agrochemicals, and organic materials. 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 synthesis of biologically active compounds, including
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 development of pharmaceuticals, agrochemicals, and organic materials. 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 synthesis of biologically active compounds, including potential drug candidates. Additionally, it finds use in the preparation of conjugated polymers and organic electronic materials, contributing to advancements in optoelectronics and photovoltaics. Its stability and reactivity make it a versatile tool in modern synthetic chemistry.
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