4-(5-Pyrimidyl)thiazole-5-boronic acid pinacol ester
95%
Reagent
Code: #90475
CAS Number
2223042-32-6
blur_circular Chemical Specifications
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Molecular Information
Weight
307.17632 g/mol
Formula
C₁₃H₁₈BN₃O₃S
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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. Its boronic ester group makes it a valuable building block for creating complex organic molecules, especially in the pharmaceutical and materials science industries. It serves as a key intermediate in the development of drugs, agrochemicals, and advanced materials. The pyrimidyl and thiazole moieties contribute to its potential use in designing biologically active compounds, including kinase inhibitors and other therapeutic agents. Its stability and reactivity make it a preferred choice for constructing heterocyclic frameworks in medicinal chemistry.
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4-(5-Pyrimidyl)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. Its boronic ester group makes it a valuable building block for creating complex organic molecules, especially in the pharmaceutical and materials science industries. It serves as a key intermediate in the development of drugs, agrochemicals, and advanced materials. The pyrimidyl and thiazole moieties contribute to its potential use in designing biologically active compounds, including kinase inhibitors and other therapeutic agents. Its stability and reactivity make it a preferred choice for constructing heterocyclic frameworks in medicinal chemistry.
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