(R)-2-Benzylpyrrolidine-2-carboxylic acid hydrochloride

98%

Reagent Code: #230688
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CAS Number 2098693-96-8

science Other reagents with same CAS 2098693-96-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.71 g/mol
Formula C₁₂H₁₆ClNO₂
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

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 a defined stereochemistry makes it valuable for designing drugs that require high selectivity and binding affinity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing peptidomimetic compounds. Also utilized in asymmetric synthesis to introduce chirality in complex molecule construction.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿16,200.00
250mg
10-20 days ฿27,010.00
1g
10-20 days ฿58,500.00
(R)-2-Benzylpyrrolidine-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 a defined stereochemistry makes it valuable for designing drugs that require high selectivity and binding affinity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing peptidomimetic compounds. Also utilized in asymmetric synthesis to introduce chirali

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 a defined stereochemistry makes it valuable for designing drugs that require high selectivity and binding affinity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing peptidomimetic compounds. Also utilized in asymmetric synthesis to introduce chirality in complex molecule construction.

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