(2S)-1-Benzylpyrrolidine-2-carboxylic acid

≥95%

Reagent Code: #234676
label
Alias 1-benzyl-L-proline;N-benzyl-L-proline;BZL-proline;(S)-1-N-benzylproline
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CAS Number 31795-93-4

science Other reagents with same CAS 31795-93-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.25 g/mol
Formula C₁₂H₁₅NO₂
badge Registry Numbers
MDL Number MFCD00235894
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 protease inhibitors and other bioactive molecules. Its stereochemistry makes it valuable in asymmetric synthesis for creating enantiomerically pure drugs. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its rigid pyrrolidine scaffold and functional handle for derivatization. Also utilized in the preparation of enzyme inhibitors targeting neurological and metabolic disorders.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,190.00
inventory 25g
10-20 days ฿6,010.00
inventory 5g
10-20 days ฿1,400.00
(2S)-1-Benzylpyrrolidine-2-carboxylic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry makes it valuable in asymmetric synthesis for creating enantiomerically pure drugs. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its rigid pyrrolidine scaffold and functional handle for derivatization. Also utilized in the preparation of enzyme inhibitors targeting neurological and meta

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry makes it valuable in asymmetric synthesis for creating enantiomerically pure drugs. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its rigid pyrrolidine scaffold and functional handle for derivatization. Also utilized in the preparation of enzyme inhibitors targeting neurological and metabolic disorders.

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