Tert-Butyl 2-Oxa-3-Azabicyclo[2.2.2]Oct-5-Ene-3-Carboxylate

95%

Reagent Code: #242837
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CAS Number 110590-29-9

science Other reagents with same CAS 110590-29-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.26 g/mol
Formula C₁₁H₁₇NO₃
badge Registry Numbers
MDL Number MFCD24038975
thermostat Physical Properties
Boiling Point 280.1±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.138±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its rigid bicyclic structure and built-in nitrogen functionality make it valuable for constructing complex molecules, especially in the development of enzyme inhibitors and receptor ligands. Commonly employed in medicinal chemistry for scaffold diversification and as a protecting group strategy in multi-step synthesis due to the stability of the tert-butyl carbamate (Boc) moiety. The compound’s alkene bridge allows for further functionalization via hydrogenation, epoxidation, or dihydroxylation, enabling versatile derivatization for drug discovery and combinatorial chemistry applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,410.00
inventory 250mg
10-20 days ฿22,500.00
inventory 1g
10-20 days ฿52,960.00

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Tert-Butyl 2-Oxa-3-Azabicyclo[2.2.2]Oct-5-Ene-3-Carboxylate
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its rigid bicyclic structure and built-in nitrogen functionality make it valuable for constructing complex molecules, especially in the development of enzyme inhibitors and receptor ligands. Commonly employed in medicinal chemistry for scaffold diversification and as a protecting group strategy in multi-step synthesis due to the stability of the tert-butyl carbamate (Boc)

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its rigid bicyclic structure and built-in nitrogen functionality make it valuable for constructing complex molecules, especially in the development of enzyme inhibitors and receptor ligands. Commonly employed in medicinal chemistry for scaffold diversification and as a protecting group strategy in multi-step synthesis due to the stability of the tert-butyl carbamate (Boc) moiety. The compound’s alkene bridge allows for further functionalization via hydrogenation, epoxidation, or dihydroxylation, enabling versatile derivatization for drug discovery and combinatorial chemistry applications.

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