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

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Reagent Code: #233461
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CAS Number 2696257-57-3

science Other reagents with same CAS 2696257-57-3

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 biologically active compounds, particularly in the development of neuroactive agents. Its structural features make it valuable in the preparation of pyrrolidine-based frameworks found in certain central nervous system modulators. Commonly employed in asymmetric synthesis due to its stereochemical stability and functional group compatibility. Also utilized in the exploration of novel therapeutic candidates targeting neurological disorders.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,100.00
inventory 250mg
10-20 days ฿1,860.00

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rel-Methyl (4aS,7aS)-6-benzylhexahydropyrano[2,3-c]pyrrole-7a(2H)-carboxylate
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Used in pharmaceutical research as a chiral intermediate for the synthesis of biologically active compounds, particularly in the development of neuroactive agents. Its structural features make it valuable in the preparation of pyrrolidine-based frameworks found in certain central nervous system modulators. Commonly employed in asymmetric synthesis due to its stereochemical stability and functional group compatibility. Also utilized in the exploration of novel therapeutic candidates targeting neurological di
Used in pharmaceutical research as a chiral intermediate for the synthesis of biologically active compounds, particularly in the development of neuroactive agents. Its structural features make it valuable in the preparation of pyrrolidine-based frameworks found in certain central nervous system modulators. Commonly employed in asymmetric synthesis due to its stereochemical stability and functional group compatibility. Also utilized in the exploration of novel therapeutic candidates targeting neurological disorders.
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