866019-47-8 Usage
Molecular structure
2-([Benzyl(methyl)amino]methyl)-3-hydroxy-6-(hydroxymethyl)-4H-pyran-4-one consists of a complex structure with various functional groups such as a benzyl group, a methyl group, an amino group, and a hydroxymethyl group, along with a pyran-4-one ring system.
Benzyl group
A phenyl ring attached to a methyl group.
Methyl group
A single carbon atom connected to three hydrogen atoms.
Amino group
A nitrogen atom bonded to two hydrogen atoms.
Hydroxymethyl group
A methyl group with a hydroxyl (OH) group attached.
Pyran-4-one ring system
The compound features a pyran-4-one ring, which is a six-membered oxygen-containing heterocycle with one oxygen atom in the ring and a ketone (carbonyl) group at the 4-position.
Antioxidant properties
The compound may help neutralize free radicals and prevent oxidative damage to cells.
Antimicrobial properties
The compound may exhibit inhibitory effects against the growth of microorganisms, such as bacteria and fungi.
Other medicinal properties
The compound may have additional therapeutic effects that are yet to be discovered.
Synthesis and chemical properties
The synthesis and chemical properties of 2-([Benzyl(methyl)amino]methyl)-3-hydroxy-6-(hydroxymethyl)-4H-pyran-4-one make it an interesting molecule for further study in the fields of medicinal chemistry and biochemistry. Researchers may explore its potential applications in drug development, understanding its mechanism of action, and investigating its interactions with biological targets.
Check Digit Verification of cas no
The CAS Registry Mumber 866019-47-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,0,1 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 866019-47:
(8*8)+(7*6)+(6*6)+(5*0)+(4*1)+(3*9)+(2*4)+(1*7)=188
188 % 10 = 8
So 866019-47-8 is a valid CAS Registry Number.
866019-47-8Relevant articles and documents
A family of hydroxypyrone ligands designed and synthesized as iron chelators
Toso, Leonardo,Crisponi, Guido,Nurchi, Valeria M.,Crespo-Alonso, Miriam,Lachowicz, Joanna I.,Santos, M. Amelia,Marques, Sergio M.,Niclos-Gutierrez, Juan,Gonzalez-Perez, Josefa M.,Dominguez-Martin, Alicia,Choquesillo-Lazarte, Duane,Szewczuk, Zbigniew
, p. 220 - 231 (2013)
The use of chelating agents for iron and aluminum in different clinical applications has found increasing attention in the last thirty years. Desferal, deferiprone and deferasirox, chelating agents nowadays in use, are based on hydroxamic groups, hydroxyl-substituted pyridinones or aromatic ring systems. With the aim of designing new chelators, we synthesized a series of kojic acid derivatives composed by two kojic units joined by linkers variously substituted. The huge advantages of these molecules are that they are easy and cheap to produce. Preliminary works on complex formation equilibria of the first group of ligands with iron and aluminium highlighted extremely good pMe values and gave evidence of the ability to scavenge iron from inside cells. On these bases a second set of bis-kojic ligands, whose linkers between the kojic chelating moieties are differentiated both in terms of type and size, has been designed, synthesized and characterized. The structural characterization of these new ligands is presented, and the protonation and ironIII complex formation equilibria studied by potentiometry, UV-Visible spectrophotometry, electrospray ionization mass (ESI-MS) and 1H NMR spectroscopy will be described and discussed.
