(S)-4-Oxopyrrolidine-2-carboxylicacidhydrochloride

98%

Reagent Code: #237798
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CAS Number 54615-47-3

science Other reagents with same CAS 54615-47-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.57 g/mol
Formula C₅H₈ClNO₃
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MDL Number MFCD21603682
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of nootropic and neuroprotective agents. It serves as an intermediate in the production of racetam-class cognitive enhancers, where the (S)-enantiomer contributes to improved biological activity. Its carboxylic acid and ketone functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for creating peptidomimetics and heterocyclic compounds. Also employed in research for studying pyrrolidone metabolism and enzyme inhibition.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,120.00
inventory 250mg
10-20 days ฿2,230.00
inventory 1g
10-20 days ฿6,330.00
inventory 10g
10-20 days ฿59,230.00
inventory 5g
10-20 days ฿31,620.00

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(S)-4-Oxopyrrolidine-2-carboxylicacidhydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of nootropic and neuroprotective agents. It serves as an intermediate in the production of racetam-class cognitive enhancers, where the (S)-enantiomer contributes to improved biological activity. Its carboxylic acid and ketone functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for creating peptidomimetics and heterocyclic compounds. Also employed in resea

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of nootropic and neuroprotective agents. It serves as an intermediate in the production of racetam-class cognitive enhancers, where the (S)-enantiomer contributes to improved biological activity. Its carboxylic acid and ketone functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for creating peptidomimetics and heterocyclic compounds. Also employed in research for studying pyrrolidone metabolism and enzyme inhibition.

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