(2-(2-methyl-2H-tetrazol-5-yl)pyridyl-5-yl)(pinacolato)boron
99%
Reagent
Code: #41398
CAS Number
1056039-83-8
blur_circular Chemical Specifications
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Molecular Information
Weight
287.12 g/mol
Formula
C₁₃H₁₈BN₅O₂
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Storage & Handling
Storage
room temperature, dry
description Product Description
This compound is primarily utilized in organic synthesis as a versatile building block for the formation of carbon-carbon bonds, particularly in cross-coupling reactions. Its boronate ester group enables efficient participation in Suzuki-Miyaura coupling, a widely used method for creating biaryl structures, which are essential in pharmaceuticals, agrochemicals, and materials science. The tetrazole moiety adds stability and can act as a bioisostere in drug design, enhancing the pharmacokinetic properties of potential therapeutic agents. Additionally, its pyridine ring provides a coordination site for metal catalysts, further facilitating its use in catalytic processes. This compound is valuable in the development of complex organic molecules, including active pharmaceutical ingredients and advanced materials.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | White to off-white to grey to yellow solid |
| Purity (%) | 98.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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