(E)-Ethyl 3-(pyrrolidin-1-yl)acrylate

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Reagent Code: #183857
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CAS Number 65651-80-1

science Other reagents with same CAS 65651-80-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.22 g/mol
Formula C₉H₁₅NO₂
badge Registry Numbers
MDL Number MFCD01075735
thermostat Physical Properties
Melting Point 43-45 °C
Boiling Point 118 °C at 1 mmHg
inventory_2 Storage & Handling
Density 1.112 g/cm3
Storage 2-8°C, light-proof, inert atmosphere

description Product Description

Used as a key intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its α,β-unsaturated ester structure with a pyrrolidine substituent makes it valuable in Michael addition reactions, enabling the formation of complex amine-containing molecules. Commonly employed in the development of bioactive compounds, including potential drug candidates targeting central nervous system disorders and inflammation. Also utilized in polymer chemistry to introduce functional groups that enhance solubility and reactivity in specialty materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,170.00
inventory 25g
10-20 days ฿38,000.00
inventory 5g
10-20 days ฿10,080.00
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(E)-Ethyl 3-(pyrrolidin-1-yl)acrylate
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Used as a key intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its α,β-unsaturated ester structure with a pyrrolidine substituent makes it valuable in Michael addition reactions, enabling the formation of complex amine-containing molecules. Commonly employed in the development of bioactive compounds, including potential drug candidates targeting central nervous system disorders and inflammation. Also utilized in polymer chemistry to introduce functional g

Used as a key intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its α,β-unsaturated ester structure with a pyrrolidine substituent makes it valuable in Michael addition reactions, enabling the formation of complex amine-containing molecules. Commonly employed in the development of bioactive compounds, including potential drug candidates targeting central nervous system disorders and inflammation. Also utilized in polymer chemistry to introduce functional groups that enhance solubility and reactivity in specialty materials.

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