(2R,4S)-4-Aminopyrrolidine-2-carboxylic acid dihydrochloride

97%

Reagent Code: #229450
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CAS Number 2829279-78-7

science Other reagents with same CAS 2829279-78-7

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scatter_plot Molecular Information
Weight 203.07 g/mol
Formula C₅H₁₂Cl₂N₂O₂
badge Registry Numbers
MDL Number MFCD09025424
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

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 rigid pyrrolidine structure with defined stereochemistry makes it valuable for designing drugs targeting enzymes and receptors where spatial orientation is critical. Commonly employed in medicinal chemistry for peptidomimetic design, enhancing metabolic stability and selectivity. Also utilized in the preparation of enzyme inhibitors due to its ability to mimic natural amino acids while resisting degradation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,850.00
inventory 250mg
10-20 days ฿14,160.00
(2R,4S)-4-Aminopyrrolidine-2-carboxylic acid dihydrochloride
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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 rigid pyrrolidine structure with defined stereochemistry makes it valuable for designing drugs targeting enzymes and receptors where spatial orientation is critical. Commonly employed in medicinal chemistry for peptidomimetic design, enhancing metabolic stability and selectivity. Also utilized in the preparation of enzyme inhibitors due to its ability
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its rigid pyrrolidine structure with defined stereochemistry makes it valuable for designing drugs targeting enzymes and receptors where spatial orientation is critical. Commonly employed in medicinal chemistry for peptidomimetic design, enhancing metabolic stability and selectivity. Also utilized in the preparation of enzyme inhibitors due to its ability to mimic natural amino acids while resisting degradation.
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