1,2-Pyrrolidinedicarboxylic acid, 4-amino-, 1-(1,1-dimethylethyl) 2-methyl ester, (2R,4S)-

≥95%

Reagent Code: #66380
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CAS Number 254881-77-1

science Other reagents with same CAS 254881-77-1

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scatter_plot Molecular Information
Weight 244.29 g/mol
Formula C₁₁H₂₀N₂O₄
badge Registry Numbers
MDL Number MFCD08704545
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the pharmaceutical and biotechnology industries as a key intermediate in the synthesis of complex molecules. Its stereochemistry, particularly the (2R,4S) configuration, makes it valuable for the production of chiral drugs, where precise molecular orientation is critical for efficacy. It is often employed in the development of protease inhibitors, which are essential in treating diseases such as HIV/AIDS and hepatitis C. Additionally, its structure allows it to act as a building block in peptide synthesis, contributing to the creation of biologically active peptides used in therapeutic applications. The compound's stability and reactivity also make it suitable for use in research and development of new medicinal compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,942.00
inventory 100mg
10-20 days ฿2,655.00
inventory 1g
10-20 days ฿10,152.00

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1,2-Pyrrolidinedicarboxylic acid, 4-amino-, 1-(1,1-dimethylethyl) 2-methyl ester, (2R,4S)-
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This compound is primarily utilized in the pharmaceutical and biotechnology industries as a key intermediate in the synthesis of complex molecules. Its stereochemistry, particularly the (2R,4S) configuration, makes it valuable for the production of chiral drugs, where precise molecular orientation is critical for efficacy. It is often employed in the development of protease inhibitors, which are essential in treating diseases such as HIV/AIDS and hepatitis C. Additionally, its structure allows it to act

This compound is primarily utilized in the pharmaceutical and biotechnology industries as a key intermediate in the synthesis of complex molecules. Its stereochemistry, particularly the (2R,4S) configuration, makes it valuable for the production of chiral drugs, where precise molecular orientation is critical for efficacy. It is often employed in the development of protease inhibitors, which are essential in treating diseases such as HIV/AIDS and hepatitis C. Additionally, its structure allows it to act as a building block in peptide synthesis, contributing to the creation of biologically active peptides used in therapeutic applications. The compound's stability and reactivity also make it suitable for use in research and development of new medicinal compounds.

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