(2R,4R)-N-Boc-4-hydroxypyrrolidine-2-carboxylic acid

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Reagent Code: #229960
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CAS Number 135042-12-5

science Other reagents with same CAS 135042-12-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.25 g/mol
Formula C₁₀H₁₇NO₅
badge Registry Numbers
MDL Number MFCD02094407
inventory_2 Storage & Handling
Storage 2~8℃, dry

description Product Description

Widely used in pharmaceutical synthesis, this compound serves as a key chiral building block for the preparation of bioactive molecules, especially protease inhibitors and antiviral agents. Its N-Boc protected nitrogen, along with free hydroxyl and carboxylic acid functionalities, allow selective reactions in multi-step syntheses. The rigid pyrrolidine scaffold with defined stereochemistry enhances stereoselectivity in drug candidates. It is particularly valuable in the development of enzyme inhibitors where precise 3D orientation is critical for activity. Commonly employed in solid-phase and solution-phase peptide-like assembly, it helps construct complex heterocyclic systems found in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿168.00
inventory 25g
10-20 days ฿2,390.00
inventory 100g
10-20 days ฿4,961.00
inventory 500g
10-20 days ฿41,920.00
inventory 5g
10-20 days ฿510.00

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(2R,4R)-N-Boc-4-hydroxypyrrolidine-2-carboxylic acid
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Widely used in pharmaceutical synthesis, this compound serves as a key chiral building block for the preparation of bioactive molecules, especially protease inhibitors and antiviral agents. Its N-Boc protected nitrogen, along with free hydroxyl and carboxylic acid functionalities, allow selective reactions in multi-step syntheses. The rigid pyrrolidine scaffold with defined stereochemistry enhances stereoselectivity in drug candidates. It is particularly valuable in the development of enzyme inhibitors w

Widely used in pharmaceutical synthesis, this compound serves as a key chiral building block for the preparation of bioactive molecules, especially protease inhibitors and antiviral agents. Its N-Boc protected nitrogen, along with free hydroxyl and carboxylic acid functionalities, allow selective reactions in multi-step syntheses. The rigid pyrrolidine scaffold with defined stereochemistry enhances stereoselectivity in drug candidates. It is particularly valuable in the development of enzyme inhibitors where precise 3D orientation is critical for activity. Commonly employed in solid-phase and solution-phase peptide-like assembly, it helps construct complex heterocyclic systems found in medicinal chemistry.

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