tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydropyridine-1(2H)-carboxylate
≥95%
Reagent
Code: #148335
CAS Number
1121057-77-9
blur_circular Chemical Specifications
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Molecular Information
Weight
309.21 g/mol
Formula
C₁₆H₂₈BNO₄
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Registry Numbers
MDL Number
MFCD18383341
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Physical Properties
Boiling Point
339.6±52.0°C at 760 mmHg
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Storage & Handling
Storage
-20°C, stored in inert gas
description Product Description
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. It enables the formation of carbon-carbon bonds, particularly for introducing dihydropyridine motifs into complex molecules. This compound is valuable in medicinal chemistry for constructing nitrogen-containing heterocycles found in pharmaceuticals and bioactive compounds. Its protected dihydropyridine structure allows for selective transformations, making it useful in multi-step synthesis of drug candidates and functional materials.
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