tert-Butyl 2-vinylpyrrolidine-1-carboxylate

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Reagent Code: #151018
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CAS Number 176324-60-0

science Other reagents with same CAS 176324-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.27 g/mol
Formula C₁₁H₁₉NO₂
badge Registry Numbers
MDL Number MFCD12923195
thermostat Physical Properties
Boiling Point 248.4±29.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.050±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its vinyl group allows for further functionalization through reactions such as hydroboration, epoxidation, or Diels-Alder cycloadditions. The tert-butyl carbamate (Boc) protecting group stabilizes the pyrrolidine nitrogen during multi-step syntheses, enabling controlled deprotection under mild acidic conditions. Commonly employed in the development of protease inhibitors and other nitrogen-containing heterocyclic compounds relevant to medicinal chemistry. Also utilized in polymer chemistry as a functional monomer for specialty materials with tailored reactivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,540.00
inventory 250mg
10-20 days ฿2,580.00
inventory 1g
10-20 days ฿9,790.00
inventory 5g
10-20 days ฿48,880.00

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tert-Butyl 2-vinylpyrrolidine-1-carboxylate
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its vinyl group allows for further functionalization through reactions such as hydroboration, epoxidation, or Diels-Alder cycloadditions. The tert-butyl carbamate (Boc) protecting group stabilizes the pyrrolidine nitrogen during multi-step syntheses, enabling controlled deprotection under mild acidic conditions. Commonly employed in the development of protease inhibitors and other

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its vinyl group allows for further functionalization through reactions such as hydroboration, epoxidation, or Diels-Alder cycloadditions. The tert-butyl carbamate (Boc) protecting group stabilizes the pyrrolidine nitrogen during multi-step syntheses, enabling controlled deprotection under mild acidic conditions. Commonly employed in the development of protease inhibitors and other nitrogen-containing heterocyclic compounds relevant to medicinal chemistry. Also utilized in polymer chemistry as a functional monomer for specialty materials with tailored reactivity.

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