(R)-3-Hydroxy-1-methylpyrrolidin-2-one

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Reagent Code: #228766
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CAS Number 614754-24-4

science Other reagents with same CAS 614754-24-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 115.13 g/mol
Formula C₅H₉NO₂
badge Registry Numbers
MDL Number MFCD15529681
thermostat Physical Properties
Boiling Point 275.9±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.234±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of drugs targeting the central nervous system. Its structural features make it valuable for creating biologically active molecules with high enantioselectivity. Commonly employed in the preparation of nootropic agents and cognitive enhancers due to its ability to mimic natural neurotransmitters. Also utilized in the design of enzyme inhibitors where stereochemistry plays a critical role in activity. Its lactam ring provides metabolic stability, enhancing the pharmacokinetic profile of derived compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,600.00
inventory 500mg
10-20 days ฿21,130.00
inventory 1g
10-20 days ฿31,680.00

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(R)-3-Hydroxy-1-methylpyrrolidin-2-one
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of drugs targeting the central nervous system. Its structural features make it valuable for creating biologically active molecules with high enantioselectivity. Commonly employed in the preparation of nootropic agents and cognitive enhancers due to its ability to mimic natural neurotransmitters. Also utilized in the design of enzyme inhibitors where stereochemistry plays a critical role in activity. Its l

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of drugs targeting the central nervous system. Its structural features make it valuable for creating biologically active molecules with high enantioselectivity. Commonly employed in the preparation of nootropic agents and cognitive enhancers due to its ability to mimic natural neurotransmitters. Also utilized in the design of enzyme inhibitors where stereochemistry plays a critical role in activity. Its lactam ring provides metabolic stability, enhancing the pharmacokinetic profile of derived compounds.

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