(R)-methyl 5-oxopyrrolidine-3-carboxylate

95%

Reagent Code: #230867
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CAS Number 443304-03-8

science Other reagents with same CAS 443304-03-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.14 g/mol
Formula C₆H₉NO₃
badge Registry Numbers
MDL Number MFCD13194687
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of nootropic drugs such as piracetam and related racetam family compounds. Its pyrrolidone structure with a reactive ketone and ester group allows for selective chemical modifications, making it valuable in developing cognitive enhancers. The (R)-enantiomer is preferred in some syntheses due to higher biological activity or better metabolic stability in the final drug product. Commonly employed in research settings for developing neuroprotective agents and compounds targeting neurological disorders.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿62,610.00
250mg
10-20 days ฿100,180.00
(R)-methyl 5-oxopyrrolidine-3-carboxylate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of nootropic drugs such as piracetam and related racetam family compounds. Its pyrrolidone structure with a reactive ketone and ester group allows for selective chemical modifications, making it valuable in developing cognitive enhancers. The (R)-enantiomer is preferred in some syntheses due to higher biological activity or better metabolic stability in the final drug product. Commonly employed in research s

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of nootropic drugs such as piracetam and related racetam family compounds. Its pyrrolidone structure with a reactive ketone and ester group allows for selective chemical modifications, making it valuable in developing cognitive enhancers. The (R)-enantiomer is preferred in some syntheses due to higher biological activity or better metabolic stability in the final drug product. Commonly employed in research settings for developing neuroprotective agents and compounds targeting neurological disorders.

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