rel-Methyl (4aS,7aR)-6-benzylhexahydropyrano[2,3-c]pyrrole-4a(2H)-carboxylate

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Reagent Code: #233229
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CAS Number 2696257-52-8

science Other reagents with same CAS 2696257-52-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.34 g/mol
Formula C₁₆H₂₁NO₃
thermostat Physical Properties
Boiling Point 360.0±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.179±0.06 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used in pharmaceutical research as a chiral intermediate for the synthesis of neuroactive compounds, particularly in the development of agents targeting central nervous system disorders. Its structural features support high enantioselectivity in synthetic pathways, making it valuable in the preparation of biologically active molecules with improved stereochemical purity. Commonly employed in medicinal chemistry for optimizing drug candidates that require fused heterocyclic scaffolds with defined stereochemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,400.00
inventory 250mg
10-20 days ฿19,380.00

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rel-Methyl (4aS,7aR)-6-benzylhexahydropyrano[2,3-c]pyrrole-4a(2H)-carboxylate
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Used in pharmaceutical research as a chiral intermediate for the synthesis of neuroactive compounds, particularly in the development of agents targeting central nervous system disorders. Its structural features support high enantioselectivity in synthetic pathways, making it valuable in the preparation of biologically active molecules with improved stereochemical purity. Commonly employed in medicinal chemistry for optimizing drug candidates that require fused heterocyclic scaffolds with defined stereoch

Used in pharmaceutical research as a chiral intermediate for the synthesis of neuroactive compounds, particularly in the development of agents targeting central nervous system disorders. Its structural features support high enantioselectivity in synthetic pathways, making it valuable in the preparation of biologically active molecules with improved stereochemical purity. Commonly employed in medicinal chemistry for optimizing drug candidates that require fused heterocyclic scaffolds with defined stereochemistry.

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