(E)-Tert-Butyl 3-(Pyridin-2-Yl)Acrylate

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Reagent Code: #184538
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CAS Number 181517-75-9

science Other reagents with same CAS 181517-75-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.25 g/mol
Formula C₁₂H₁₅NO₂
badge Registry Numbers
MDL Number MFCD22205823
thermostat Physical Properties
Boiling Point 352.7±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.062±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals, particularly in the development of pyridine-containing compounds. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and cross-coupling reactions. Commonly employed in the preparation of biologically active molecules, including kinase inhibitors and anti-inflammatory agents. Also utilized in materials science for constructing functionalized polymers and ligands for metal catalysts. The tert-butyl ester group allows for easy deprotection under mild acidic conditions, enabling stepwise synthesis in complex molecule assembly.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,840.00
inventory 250mg
10-20 days ฿25,430.00
inventory 1g
10-20 days ฿50,860.00

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(E)-Tert-Butyl 3-(Pyridin-2-Yl)Acrylate
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Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals, particularly in the development of pyridine-containing compounds. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and cross-coupling reactions. Commonly employed in the preparation of biologically active molecules, including kinase inhibitors and anti-inflammatory agents. Also utilized in materials science for constructing functionalized polymers and ligands for metal catalysts. The te

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals, particularly in the development of pyridine-containing compounds. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and cross-coupling reactions. Commonly employed in the preparation of biologically active molecules, including kinase inhibitors and anti-inflammatory agents. Also utilized in materials science for constructing functionalized polymers and ligands for metal catalysts. The tert-butyl ester group allows for easy deprotection under mild acidic conditions, enabling stepwise synthesis in complex molecule assembly.

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