Diethyl 4-vinylpyridine-2,6-dicarboxylate

95%

Reagent Code: #176913
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CAS Number 1887093-15-3

science Other reagents with same CAS 1887093-15-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.3 g/mol
Formula C₁₃H₁₅NO₄
inventory_2 Storage & Handling
Storage 2-8°C, dry, closed

description Product Description

Used as a key intermediate in the synthesis of functional polymers and specialty resins, particularly in the development of catalysts and ligands for transition metal complexes. Its vinyl and pyridine groups enable copolymerization with various monomers, making it valuable in creating tailored materials for catalysis, sensors, and adsorption applications. The compound also serves in surface modification of polymers and silica due to its ability to introduce nitrogen-containing functional sites. Its ester groups allow further chemical transformations, enhancing utility in organic and polymer chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿54,340.00

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Diethyl 4-vinylpyridine-2,6-dicarboxylate
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Used as a key intermediate in the synthesis of functional polymers and specialty resins, particularly in the development of catalysts and ligands for transition metal complexes. Its vinyl and pyridine groups enable copolymerization with various monomers, making it valuable in creating tailored materials for catalysis, sensors, and adsorption applications. The compound also serves in surface modification of polymers and silica due to its ability to introduce nitrogen-containing functional sites. Its ester

Used as a key intermediate in the synthesis of functional polymers and specialty resins, particularly in the development of catalysts and ligands for transition metal complexes. Its vinyl and pyridine groups enable copolymerization with various monomers, making it valuable in creating tailored materials for catalysis, sensors, and adsorption applications. The compound also serves in surface modification of polymers and silica due to its ability to introduce nitrogen-containing functional sites. Its ester groups allow further chemical transformations, enhancing utility in organic and polymer chemistry research.

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