Ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate
96%
Reagent
Code: #185014
CAS Number
916326-10-8
blur_circular Chemical Specifications
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Molecular Information
Weight
277.12 g/mol
Formula
C₁₄H₂₀BNO₄
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Registry Numbers
MDL Number
MFCD04117940
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Storage & Handling
Storage
2-8°C, Inert Gas
description Product Description
Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing biaryl and heteroaryl frameworks in pharmaceutical and agrochemical synthesis. Its boronate ester group enables efficient and selective carbon-carbon bond formation under mild conditions. Commonly employed in late-stage functionalization of complex molecules, it allows introduction of a pyridine-carboxylate motif, which is valuable in drug discovery for modulating solubility, binding affinity, and metabolic stability. It is also used in materials science for synthesizing conjugated organic systems, such as those found in OLEDs and organic semiconductors.
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