4-(diisopropylcarbaMoyl)-2-ethoxypyridin-3-ylboronic acid
95%
Reagent
Code: #90529
Alias
4-(Diisopropylcarbamoyl)-2-ethoxypyridin-3-ylboronic acid
CAS Number
1131735-94-8
blur_circular Chemical Specifications
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Molecular Information
Weight
294.16 g/mol
Formula
C₁₄H₂₃BN₂O₄
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Storage & Handling
Storage
2~8 ℃
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. Its application is significant in pharmaceutical research and development, where it aids in the synthesis of drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it is used in material science for creating advanced polymers and functional materials with tailored properties. The ethoxy and diisopropylcarbamoyl groups enhance its stability and reactivity, making it a valuable tool in precision chemical synthesis.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity | 94.5-100% |
Appearance | Yellow solid |
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4-(diisopropylcarbaMoyl)-2-ethoxypyridin-3-ylboronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. Its application is significant in pharmaceutical research and development, where it aids in the synthesis of drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it is used in material science for creating advanced polymers and functional materials with tailored properties. The ethoxy and diisopropylcarbamoyl groups enhance its stability and reactivity, making it a valuable tool in precision chemical synthesis.
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