(2S,4R)-4-Phenylpyrrolidine-2-carboxylic acid hydrochloride

95%

Reagent Code: #236247
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CAS Number 82087-67-0

science Other reagents with same CAS 82087-67-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.69 g/mol
Formula C₁₁H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD17976749
inventory_2 Storage & Handling
Storage 2-8°C

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 stereo-selectivity is critical. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in CNS-related drug discovery and antiviral research. Also utilized in asymmetric synthesis to introduce chirality in complex molecule construction.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,210.00
inventory 250mg
10-20 days ฿7,430.00
inventory 1g
10-20 days ฿14,870.00
(2S,4R)-4-Phenylpyrrolidine-2-carboxylic acid hydrochloride
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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 stereo-selectivity is critical. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in CNS-related drug discovery and antiviral research. Also utilized in asymmetric

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 stereo-selectivity is critical. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in CNS-related drug discovery and antiviral research. Also utilized in asymmetric synthesis to introduce chirality in complex molecule construction.

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