870537-65-8 Usage
Molecular structure
The compound has a complex molecular structure that includes a phenylmethyl ester group, a chloroacetyl group, and a 10-oxa-2,5,8-triazadodecanoic acid backbone.
Atom composition
The compound is composed of oxygen, nitrogen, carbon, hydrogen, and chlorine atoms.
Stereochemistry
The compound has a 4S and 7S configuration, which refers to the spatial arrangement of the atoms in the molecule.
Potential applications
The compound has potential applications in pharmaceuticals, chemical synthesis, and other industries due to its unique structure and properties.
Solubility
The compound is likely to be soluble in organic solvents such as ethanol, methanol, and acetone.
Stability
The compound may be sensitive to light, heat, and moisture, and should be stored in a cool, dry place.
Reactivity
The compound may react with strong acids, bases, and nucleophiles.
Purity
The compound may be synthesized with a high degree of purity, which is important for its potential applications.
Structural analysis
The compound's structure can be analyzed using techniques such as nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry.
Synthesis
The compound can be synthesized through a series of chemical reactions, including esterification, acylation, and cyclization reactions.
It's important to note that this is a complex compound and further research and analysis would be needed to fully understand its properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 870537-65-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,5,3 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 870537-65:
(8*8)+(7*7)+(6*0)+(5*5)+(4*3)+(3*7)+(2*6)+(1*5)=188
188 % 10 = 8
So 870537-65-8 is a valid CAS Registry Number.
870537-65-8Relevant academic research and scientific papers
Studies on the mechanism of 1,2-dihydropyrazin-2-one ring formation from dipeptidyl chloromethyl ketone and its chemical properties: Immediate deamination during catalytic hydrogenation
Miyazaki, Anna,Fujisawa, Yutaka,Shiotani, Kimitaka,Fujita, Yoshio,Li, Tingyou,Tsuda, Yuko,Yokoi, Toshio,Bryant, Sharon D.,Lazarus, Lawrence H.,Okada, Yoshio
, p. 1152 - 1158 (2007/10/03)
1,2-Dihydropyrazin-2-one derivatives, which have two aminoalkyl groups at the positions 3 and 6, were found to be efficient tools for the construction of potent, selective and long-acting opioid mimetics. During the course of preparation, we found that the catalytic hydrogenation of 3,6- bis(benzyloxycarbonylaminomethyl)-5-methyl-1,2-dihydropyrazin-2-one to remove the benzyloxycarbonyl groups resulted in a side reaction. By MS and NMR studies and by preparation of additional 1,2-dihydropyrazin-2-one derivatives, the structure of the by-product was identified as 3-aminomethyl-5,6-dimethyl-1,2- dihydropyrazin-2-one. Preparation of additional compounds substituted with deuterium provided us with sufficient information to confirm the structure of the product and to support a cyclization mechanism in its formation.
