Hexahydro-2H-Cyclopenta[d]Oxazol-2-One

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Reagent Code: #196410
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CAS Number 114364-42-0

science Other reagents with same CAS 114364-42-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 127.14 g/mol
Formula C₆H₉NO₂
badge Registry Numbers
MDL Number MFCD19218341
thermostat Physical Properties
Boiling Point 353.1±9.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.193±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the development of pharmaceuticals due to its rigid bicyclic structure and functional group compatibility. Its lactam-like framework is valuable in constructing bioactive molecules, particularly in medicinal chemistry for central nervous system agents. The compound’s stability and reactivity profile make it suitable for ring-opening, functionalization, and coupling reactions in multi-step synthesis. It is also explored in the design of enzyme inhibitors where conformational restraint enhances binding affinity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,010.00
inventory 250mg
10-20 days ฿22,770.00
inventory 1g
10-20 days ฿45,550.00

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Hexahydro-2H-Cyclopenta[d]Oxazol-2-One
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Used primarily as an intermediate in organic synthesis, this compound serves in the development of pharmaceuticals due to its rigid bicyclic structure and functional group compatibility. Its lactam-like framework is valuable in constructing bioactive molecules, particularly in medicinal chemistry for central nervous system agents. The compound’s stability and reactivity profile make it suitable for ring-opening, functionalization, and coupling reactions in multi-step synthesis. It is also explored in the de
Used primarily as an intermediate in organic synthesis, this compound serves in the development of pharmaceuticals due to its rigid bicyclic structure and functional group compatibility. Its lactam-like framework is valuable in constructing bioactive molecules, particularly in medicinal chemistry for central nervous system agents. The compound’s stability and reactivity profile make it suitable for ring-opening, functionalization, and coupling reactions in multi-step synthesis. It is also explored in the design of enzyme inhibitors where conformational restraint enhances binding affinity.
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