7093-70-1

Basic information

• Product Name: GLYCYL-L-THREONINE
• Synonyms: (2S,3R)-2-[(2-aminoacetyl)amino]-3-hydroxybutanoic acid;Glycyl-L-threonine Dihydrate;L-Threonine, N-glycyl-;N-(Aminoacetyl)threonine;H-GLY-THR-OH;GLYCYL-L-THREONINE;GLY-L-THR;GLY-THR
• CAS NO: 7093-70-1
• Molecular Formula: C₆H₁₂N₂O₄
• Molecular Weight: 176.17
• EINECS: 230-399-9
• Product Categories: Biochemistry;Oligopeptides;Peptide Synthesis
• Mol File: 7093-70-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 486.7°Cat760mmHg
• Flash Point: 248.2°C
• Appearance: /
• Density: 1.354g/cm³
• Vapor Pressure: 1.62E-11mmHg at 25°C
• Refractive Index: 1.527
• Storage Temp.: -15°C
• PKA: 2.98±0.10(Predicted)
• Water Solubility: almost transparency
• CAS DataBase Reference: GLYCYL-L-THREONINE(CAS DataBase Reference)
• NIST Chemistry Reference: GLYCYL-L-THREONINE(7093-70-1)
• EPA Substance Registry System: GLYCYL-L-THREONINE(7093-70-1)

Safety Data

• Hazardous Substances Data: 7093-70-1(Hazardous Substances Data)

Usage

Definition

ChEBI: A dipeptide formed from glycine and L-threonine residues.

InChI:InChI=1/C6H12N2O4/c1-3(9)5(6(11)12)8-4(10)2-7/h3,5,9H,2,7H2,1H3,(H,8,10)(H,11,12)/t3-,5+/m1/s1

Upstream product

• 153893-46-0 N-chloroacetyl-L-threonine 
• 29022-11-5 N-(fluoren-9-ylmethoxycarbonyl)glycine 
• 73731-37-0 Fmoc-Thr-OH 

Downstream Products

• 72-19-5 L-threonine 
• 56-40-6 glycine 

Relevant articles and documents

Stomata-like metal peptide coordination polymer

The water-triggered reversible transformation plays a significant role in bio-systems. To develop artificial materials with reversible structural transformability under mild conditions would be helpful to understand how bio-systems work. Here we report on a flexible coordination polymer, Cu-(Gly-Thr)·2H2O, whose structure can be controlled by humidity or temperature. This porous coordination polymer shows reversible single-crystal to single-crystal transformation with surprisingly high thermal stability. It was found that the ordered transformation occurs via coordination bonds breaking and reforming without changing the coordination numbers and valence of the copper ion. This reversible transformation makes it especially efficient at taking up CO2 under wet conditions, which is similar to the function of plant stomata.