874163-04-9

Basic information

• Product Name: 1-Pyrrolidinecarboxylic acid, 2-[[[(3R)-1-(2-amino-2-oxoethyl)-2-oxo-3-pyrrolidinyl]amino]carbonyl]-4-[ [(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (2S,4S)-
• CAS NO: 874163-04-9
• Molecular Formula: C24H33N5O7
• Molecular Weight: 503.555
• Mol File: 874163-04-9.mol

Chemical Properties

• CAS DataBase Reference: 1-Pyrrolidinecarboxylic acid, 2-[[[(3R)-1-(2-amino-2-oxoethyl)-2-oxo-3-pyrrolidinyl]amino]carbonyl]-4-[ [(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (2S,4S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Pyrrolidinecarboxylic acid, 2-[[[(3R)-1-(2-amino-2-oxoethyl)-2-oxo-3-pyrrolidinyl]amino]carbonyl]-4-[ [(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (2S,4S)-(874163-04-9)
• EPA Substance Registry System: 1-Pyrrolidinecarboxylic acid, 2-[[[(3R)-1-(2-amino-2-oxoethyl)-2-oxo-3-pyrrolidinyl]amino]carbonyl]-4-[ [(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (2S,4S)-(874163-04-9)

Safety Data

• Hazardous Substances Data: 874163-04-9(Hazardous Substances Data)

Usage

Molecular structure

A complex structure containing a pyrrolidine ring, with various functional groups attached.

Functional groups

Amino (NH2) groups
Carbonyl (C=O) groups
Ester (R-COO-R') groups

Chirality

The compound has two chiral centers, indicated by (2S,4S) notation, which means it has non-superimposable mirror images (enantiomers).

Derivative

It is a derivative of 1-pyrrolidinecarboxylic acid, meaning it is a modified version of the parent compound.

Synthetic compound

It is a man-made chemical, and its properties and uses are not widely known.

Potential applications

Based on its chemical structure, it may have potential applications in pharmaceuticals or organic synthesis.

Further research

More research and testing are needed to fully understand its properties and potential uses.

Upstream product

• 89813-47-8 N-(tert-butoxycarbonyl)-(2S,4R)-4-hydroxyproline benzyl ester 
• 132622-66-3 cis-1-(1,1-dimethylethyoxycarbonyl)-4-amino-L-proline 
• 874162-99-9 (2S,4S)-4-(((benzyloxy)carbonyl)amino)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid 
• 865295-35-8 2-benzyl 1-(tert-butyl) (2S,4R)-4-((methylsulfonyl)oxy)pyrrolidine-1,2-dicarboxylate 
• 874162-96-6 (2S,4S)-2-benzyl 1-tert-butyl 4-azidopyrrolidine-1,2-dicarboxylate 
• 874163-02-7 methyl 3(R)-[(4(S)-(4-benzyloxycarbonylamino)-1-(tert-butoxycarbonyl)-2(S)-pyrrolidinylcarbonyl)amino]-2-oxo-1-pyrrolidineacetate 

Downstream Products

• 874163-08-3 3(R)-[(4(S)-((4-azido-2-hydroxy-5-iodobenzoyl)amino)-1-(tert-butoxycarbonyl)-2(S)-pyrrolidinylcarbonyl)amino]-2-oxo-1-pyrrolidineacetamide 
• 874163-07-2 3(R)-[(4(S)-((4-azido-2-hydroxybenzoyl)amino)-1-(tert-butoxycarbonyl)-2(S)-pyrrolidinylcarbonyl)amino]-2-oxo-1-pyrrolidineacetamide 
• 874163-06-1 3(R)-[(4(S)-((4-azidobenzoyl)amino)-1-(tert-butoxycarbonyl)-2(S)-pyrrolidinylcarbonyl)amino]-2-oxo-1-pyrrolidineacetamide 

Relevant articles and documents

Design and synthesis of photoaffinity-labeling ligands of the L-prolyl-L-leucylglycinamide binding site involved in the allosteric modulation of the dopamine receptor

Pro-Leu-Gly-NH2 (PLG), in addition to its endocrine effects, possesses the ability to modulate dopamine 02 receptors within the central nervous system. However, the precise binding site of PLG is unknown. Potential photoaffinity-labeling ligand