(1S,3S,5S)-tert-Butyl 3-carbamoyl-2-azabicyclo[3.1.0]hexane-2-carboxylate

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Reagent Code: #236381
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CAS Number 361440-67-7

science Other reagents with same CAS 361440-67-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.27 g/mol
Formula C₁₁H₁₈N₂O₃
badge Registry Numbers
MDL Number MFCD13151933
thermostat Physical Properties
Boiling Point 388.9 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.228 g/cm3
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other biologically active molecules. Its rigid bicyclic structure and functional groups make it valuable for constructing stereochemically defined compounds, especially in medicinal chemistry for optimizing drug potency and metabolic stability. Commonly employed in the preparation of enzyme inhibitors where precise spatial orientation of functional moieties is critical. Also utilized in research settings for scaffold development in peptidomimetic design.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿490.00
inventory 5g
10-20 days ฿2,290.00
inventory 25g
10-20 days ฿11,350.00
inventory 100g
10-20 days ฿37,670.00

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(1S,3S,5S)-tert-Butyl 3-carbamoyl-2-azabicyclo[3.1.0]hexane-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other biologically active molecules. Its rigid bicyclic structure and functional groups make it valuable for constructing stereochemically defined compounds, especially in medicinal chemistry for optimizing drug potency and metabolic stability. Commonly employed in the preparation of enzyme inhibitors where precise spatial orientation of functional moieties is critical. Also utili
Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other biologically active molecules. Its rigid bicyclic structure and functional groups make it valuable for constructing stereochemically defined compounds, especially in medicinal chemistry for optimizing drug potency and metabolic stability. Commonly employed in the preparation of enzyme inhibitors where precise spatial orientation of functional moieties is critical. Also utilized in research settings for scaffold development in peptidomimetic design.
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