Methyl (2S,4S)-4-hydroxypyrrolidine-2-carboxylate hydrochloride

98%

Reagent Code: #207036
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CAS Number 40126-30-5

science Other reagents with same CAS 40126-30-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.62 g/mol
Formula C₆H₁₂ClNO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a chiral building block for the synthesis of bioactive molecules, particularly in the development of protease inhibitors and neurologically active compounds. Its hydroxyl and methyl ester functional groups allow for versatile chemical modifications, making it valuable in medicinal chemistry for constructing peptidomimetics and other drug-like structures. The compound's rigid pyrrolidine scaffold with defined stereochemistry supports the design of high-affinity ligands targeting enzymes and receptors. It is also employed in the preparation of prodrugs and in structure-activity relationship (SAR) studies to optimize pharmacokinetic properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿1,430.00
10g
10-20 days ฿2,310.00
25g
10-20 days ฿6,040.00
Methyl (2S,4S)-4-hydroxypyrrolidine-2-carboxylate hydrochloride
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Used in pharmaceutical research as a chiral building block for the synthesis of bioactive molecules, particularly in the development of protease inhibitors and neurologically active compounds. Its hydroxyl and methyl ester functional groups allow for versatile chemical modifications, making it valuable in medicinal chemistry for constructing peptidomimetics and other drug-like structures. The compound's rigid pyrrolidine scaffold with defined stereochemistry supports the design of high-affinity ligands t

Used in pharmaceutical research as a chiral building block for the synthesis of bioactive molecules, particularly in the development of protease inhibitors and neurologically active compounds. Its hydroxyl and methyl ester functional groups allow for versatile chemical modifications, making it valuable in medicinal chemistry for constructing peptidomimetics and other drug-like structures. The compound's rigid pyrrolidine scaffold with defined stereochemistry supports the design of high-affinity ligands targeting enzymes and receptors. It is also employed in the preparation of prodrugs and in structure-activity relationship (SAR) studies to optimize pharmacokinetic properties.

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