3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,5-naphthyridine
95%
Reagent
Code: #44319
CAS Number
1356165-79-1
blur_circular Chemical Specifications
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Molecular Information
Weight
256.1080 g/mol
Formula
C₁₄H₁₇BN₂O₂
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Registry Numbers
MDL Number
MFCD13182107
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Storage & Handling
Storage
2-8°C
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 key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it valuable for creating biologically active compounds, including drug candidates. Additionally, it is employed in materials science for the development of organic electronic materials and polymers. Its stability and reactivity make it a versatile reagent in modern synthetic chemistry.
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