5-(5-Pyrimidyl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90819
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CAS Number 1402173-96-9

science Other reagents with same CAS 1402173-96-9

blur_circular Chemical Specifications

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Weight 306.18826 g/mol
Formula C₁₄H₁₉BN₂O₃S
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 key intermediate for creating complex organic molecules, especially in the pharmaceutical and materials science fields. Its boronic ester group enables efficient coupling with aryl halides, facilitating the construction of biaryl structures. This is essential in developing drugs, agrochemicals, and advanced materials like organic semiconductors. The pyrimidyl and thiophene moieties contribute to its role in designing compounds with specific electronic or biological properties, making it valuable in medicinal chemistry and optoelectronic applications.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,080.00
inventory 25mg
10-20 days ฿29,304.00

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5-(5-Pyrimidyl)thiophene-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 key intermediate for creating complex organic molecules, especially in the pharmaceutical and materials science fields. Its boronic ester group enables efficient coupling with aryl halides, facilitating the construction of biaryl structures. This is essential in developing drugs, agrochemicals, and advanced materials like organic semiconductors. The pyrimidyl and thiophene moieti
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for creating complex organic molecules, especially in the pharmaceutical and materials science fields. Its boronic ester group enables efficient coupling with aryl halides, facilitating the construction of biaryl structures. This is essential in developing drugs, agrochemicals, and advanced materials like organic semiconductors. The pyrimidyl and thiophene moieties contribute to its role in designing compounds with specific electronic or biological properties, making it valuable in medicinal chemistry and optoelectronic applications.
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