959581-73-8

Basic information

• Product Name: Boc-(S)-α-(4-nitro-benzyl)-proline
• Synonyms: Boc-(S)-α-(4-nitro-benzyl)-proline;(Tert-Butoxy)Carbonyl (S)-Alpha-(4-nitro-benzyl)-Pro
• CAS NO: 959581-73-8
• Molecular Formula: C17H22N2O6
• Molecular Weight: 350.36638
• Mol File: 959581-73-8.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Boc-(S)-α-(4-nitro-benzyl)-proline(CAS DataBase Reference)
• NIST Chemistry Reference: Boc-(S)-α-(4-nitro-benzyl)-proline(959581-73-8)
• EPA Substance Registry System: Boc-(S)-α-(4-nitro-benzyl)-proline(959581-73-8)

Safety Data

• Hazardous Substances Data: 959581-73-8(Hazardous Substances Data)

Usage

Description

(S)-1-(tert-Butoxycarbonyl)-2-(4-nitrobenzyl)pyrrolidine-2-carboxylic acid is a complex chemical compound that features a pyrrolidine ring and a carboxylic acid group. The (S)-1-(tert-Butoxycarbonyl) group serves as a protective agent in chemical synthesis, shielding the molecule from unwanted reactions. Additionally, the 4-nitrobenzyl group endows the compound with potential applications in the synthesis of peptides and other bioactive molecules, making it a valuable asset in pharmaceutical development and organic chemistry.

Uses

Used in Pharmaceutical Development:
(S)-1-(tert-Butoxycarbonyl)-2-(4-nitrobenzyl)pyrrolidine-2-carboxylic acid is used as a precursor in the synthesis of bioactive molecules for pharmaceutical applications. Its unique structure and functional groups allow for the creation of new drugs with potential therapeutic benefits.
Used in Organic Chemistry:
In the field of organic chemistry, (S)-1-(tert-Butoxycarbonyl)-2-(4-nitrobenzyl)pyrrolidine-2-carboxylic acid is used as a building block for the development of complex organic molecules. Its versatile structure and protective group make it a valuable component in the synthesis of various organic compounds.
Used in Peptide Synthesis:
(S)-1-(tert-Butoxycarbonyl)-2-(4-nitrobenzyl)pyrrolidine-2-carboxylic acid is used as a key intermediate in the synthesis of peptides. The presence of the 4-nitrobenzyl group facilitates the formation of peptide bonds, making it an essential component in the production of peptide-based drugs and therapeutic agents.
Used in Chemical Synthesis as a Protecting Group:
The (S)-1-(tert-Butoxycarbonyl) modification in this compound is used as a protecting group during chemical synthesis. It helps prevent unwanted side reactions, ensuring the successful synthesis of the desired product with minimal impurities and side products.