56672-63-0 Usage
General Description
Cbz-L-arginine hydrochloride is a chemical compound that is derived from the amino acid L-arginine. It consists of L-arginine that has been modified by the addition of a carbobenzyloxy (Cbz) group and a hydrochloride salt. This modification makes the compound more stable and suitable for use in pharmaceutical applications. Cbz-L-arginine hydrochloride has been studied for its potential in drug delivery systems and as a building block for the synthesis of other compounds. It is also used as a research tool in the study of amino acid chemistry and peptide synthesis. Overall, Cbz-L-arginine hydrochloride is an important chemical in the field of pharmaceutical and biochemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 56672-63-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,7 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56672-63:
(7*5)+(6*6)+(5*6)+(4*7)+(3*2)+(2*6)+(1*3)=150
150 % 10 = 0
So 56672-63-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N4O4/c15-13(16)17-8-4-7-11(12(19)20)18-14(21)22-9-10-5-2-1-3-6-10/h1-3,5-6,11H,4,7-9H2,(H,18,21)(H,19,20)(H4,15,16,17)
56672-63-0Relevant articles and documents
Interaction of arginine-based cationic surfactants with lipid membranes. An experimental and molecular simulation study
Almeidaa, Joao A. S.,Morana, Maria C.,Infanteb, Maria R.,Paisa, Alberto A. C. C.
scheme or table, p. 34 - 50 (2010/08/22)
The effect of two arginine-based cationic surfactants, arginine N-lauroyl amide dihydrochloride and arginine O-lauroyl ester dihydrochloride, upon dipalmitoylphosphatidylcholine liposomes, is addressed in this work. Some aspects concerning the synthesis of these surfactants are also presented in some detail. Differential scanning calorimetry, as well as fluorescence anisotropy using several probes, is used to assess the relative effects on the lipid model membranes. In spite of the structural similarity among these molecules, which differ only by the group that connects the polar head to the tail, experimental results suggest differences in their behavior. Molecular dynamics simulation provides significant insight into the molecular mechanism that governs this interaction. A rationale is provided in terms of lipid-surfactant hydrogen bonding and the consequent positioning of the surfactant molecule within the bilayer.
