Cis-2-Benzylhexahydropyrano[3,4-C]Pyrrol-4(2H)-One

95%

Reagent Code: #82785
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CAS Number 133745-53-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.29 g/mol
Formula C₁₄H₁₇NO₂
badge Registry Numbers
MDL Number MFCD28390366
thermostat Physical Properties
Boiling Point 384.8±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.170±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active molecules. Its unique structure, featuring a fused pyran-pyrrolone ring system, makes it a valuable building block for the development of complex heterocyclic compounds. These heterocycles are often explored for their potential applications in medicinal chemistry, particularly in the design of drugs targeting neurological disorders, inflammation, and infectious diseases. Additionally, the compound's benzyl group provides a site for further functionalization, enabling the creation of diverse derivatives with tailored biological activities. Its role in facilitating the synthesis of novel therapeutic agents underscores its importance in drug discovery and development processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days $603.40
inventory 250mg
10-20 days $1,055.94
inventory 1g
10-20 days $2,111.89
Cis-2-Benzylhexahydropyrano[3,4-C]Pyrrol-4(2H)-One
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active molecules. Its unique structure, featuring a fused pyran-pyrrolone ring system, makes it a valuable building block for the development of complex heterocyclic compounds. These heterocycles are often explored for their potential applications in medicinal chemistry, particularly in the design of drugs targeting neurological disorders, inflammation, and infectious diseases. Additionally, the compound's benzyl group provides a site for further functionalization, enabling the creation of diverse derivatives with tailored biological activities. Its role in facilitating the synthesis of novel therapeutic agents underscores its importance in drug discovery and development processes.
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