(2S)-[[[(PHENYLMETHOXY)CARBONYL]AMINO]METHYL]-1-PYRROLIDINECARBOXYLIC ACID 1,1-DIMETHYLETHYL ESTER

97%

Reagent Code: #235964
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CAS Number 929048-08-8

science Other reagents with same CAS 929048-08-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.41 g/mol
Formula C₁₈H₂₆N₂O₄
inventory_2 Storage & Handling
Density 1.137g/cm3
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical peptides, particularly in the production of protease inhibitors such as those used in antiviral medications. Its primary role is to protect specific functional groups during peptide coupling reactions, allowing selective bond formation in complex molecules. Commonly employed in solid-phase peptide synthesis due to its compatibility with Fmoc and Boc strategies. Also utilized in the development of enzyme inhibitors where stereochemical control is critical for biological activity.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿10,250.00
(2S)-[[[(PHENYLMETHOXY)CARBONYL]AMINO]METHYL]-1-PYRROLIDINECARBOXYLIC ACID 1,1-DIMETHYLETHYL ESTER
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Used as a key intermediate in the synthesis of pharmaceutical peptides, particularly in the production of protease inhibitors such as those used in antiviral medications. Its primary role is to protect specific functional groups during peptide coupling reactions, allowing selective bond formation in complex molecules. Commonly employed in solid-phase peptide synthesis due to its compatibility with Fmoc and Boc strategies. Also utilized in the development of enzyme inhibitors where stereochemical control

Used as a key intermediate in the synthesis of pharmaceutical peptides, particularly in the production of protease inhibitors such as those used in antiviral medications. Its primary role is to protect specific functional groups during peptide coupling reactions, allowing selective bond formation in complex molecules. Commonly employed in solid-phase peptide synthesis due to its compatibility with Fmoc and Boc strategies. Also utilized in the development of enzyme inhibitors where stereochemical control is critical for biological activity.

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