13716-89-7

Basic information

• Product Name: H-GLU-GLY-OH
• Synonyms: L-ALPHA-GLUTAMYL-GLYCINE;H-GLU-GLY-OH;ALPHA-L-GLU-GLY;L-A-GLUTAMYL-GLYCINE
• CAS NO: 13716-89-7
• Molecular Formula: C7H12N2O5
• Molecular Weight: 204.18
• Mol File: 13716-89-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 589 °C at 760 mmHg
• Flash Point: 310 °C
• Appearance: /
• Density: 1.424 g/cm³
• Vapor Pressure: 2.12E-15mmHg at 25°C
• Refractive Index: 1.536
• Storage Temp.: -15°C
• CAS DataBase Reference: H-GLU-GLY-OH(CAS DataBase Reference)
• NIST Chemistry Reference: H-GLU-GLY-OH(13716-89-7)
• EPA Substance Registry System: H-GLU-GLY-OH(13716-89-7)

Safety Data

• Hazardous Substances Data: 13716-89-7(Hazardous Substances Data)

Usage

Chemical Properties

White to off-white powder

InChI:InChI=1/C7H12N2O5/c8-4(1-2-5(10)11)7(14)9-3-6(12)13/h4H,1-3,8H2,(H,9,14)(H,10,11)(H,12,13)

Upstream product

• 1634-89-5 Z-(S)-Glu-Gly 
• 7384-33-0 N-[N-(toluene-4-sulfonyl)-L-α-glutamyl]-glycine 
• 55878-80-3 N-trityl-L-glutamic acid 5-methyl ester 
• 459-73-4 GlyOEt*HCl 
• 14687-80-0 Glu(OMe)-Gly 
• 30960-05-5 (S)-4-(((benzyloxy)carbonyl)amino)-5-((2-(tert-butoxy)-2-oxoethyl)amino)-5-oxopentanoic acid 
• 103326-27-8 N-trityl-L-glutamic acid-1-benzyl ester-5-methyl ester 
• 4561-10-8 L-glutamic acid dibenzyl ester hydrochloride 
• 15149-57-2 Z-L-Glu(OEt)-Gly-OEt 
• 4587-40-0 N-(N-benzyloxycarbonyl-α-L-glutamyl)-glycine ethyl ester 
• 4124-76-9 N-(benzyloxycarbonyl)-L-glutamic acid anhydride 
• 4816-80-2 N-tosyl-L-glutamic acid 
• 108541-02-2 5-oxo-1-(toluene-4-sulfonyl)-L-prolyl chloride 
• 114554-58-4 N-[N-(toluene-4-sulfonyl)-L-pyroglutamyl]-glycine 

Downstream Products

• 56-86-0 L-glutamic acid 
• 56-40-6 glycine 

Relevant articles and documents

Ester-mediated peptide formation promoted by deep eutectic solvents: a facile pathway to proto-peptides

The ester-amide exchange reaction enables spontaneous formation of prebiotic proto-peptides under mild conditions. However, this reaction also leads to oligomers with a vast sequence diversity of ester and amide linkages. Here, we demonstrate using deep eutectic solvents as a universal strategy to regulate the reaction pathways and promote the formation of amino acid-enriched oligomers with peptide backbones.