4-(2-Furyl)thiazole-5-boronic acid pinacol ester

95%

Reagent Code: #90341
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CAS Number 2223011-19-4

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scatter_plot Molecular Information
Weight 295.16232 g/mol
Formula C₁₃H₁₈BNO₄S
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 building block for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic ester group facilitates its use in coupling with aryl or vinyl halides, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its furyl and thiazole moieties contribute to its potential application in the development of bioactive compounds, including drug candidates targeting various diseases. 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 5mg
10-20 days ฿10,080.00
inventory 25mg
10-20 days ฿29,304.00
4-(2-Furyl)thiazole-5-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic ester group facilitates its use in coupling with aryl or vinyl halides, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its furyl and thiazole moieties contribute to its potential application in the development of bioactive compounds, including drug candidates targeting various diseases. Its stability and reactivity make it a versatile reagent in medicinal chemistry and material science research.
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