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Home > Imidazoles > 1192-34-3
1192-34-3 | 2H-Imidazol-2-one, 1,3-dihydro-4-methyl-
CAS No: 1192-34-3 Catalog No: AG000ICN MDL No:MFCD00233011
Product Description
Catalog Number:
AG000ICN
Chemical Name:
2H-Imidazol-2-one, 1,3-dihydro-4-methyl-
CAS Number:
1192-34-3
Molecular Formula:
C4H6N2O
Molecular Weight:
98.1032
MDL Number:
MFCD00233011
IUPAC Name:
4-methyl-1,3-dihydroimidazol-2-one
InChI:
InChI=1S/C4H6N2O/c1-3-2-5-4(7)6-3/h2H,1H3,(H2,5,6,7)
InChI Key:
MCSCIFLXNFLCDV-UHFFFAOYSA-N
SMILES:
Cc1c[nH]c(=O)[nH]1
EC Number:
214-751-9
NSC Number:
186756
Properties
Complexity:
128
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
98.048g/mol
Formal Charge:
0
Heavy Atom Count:
7
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
98.105g/mol
Monoisotopic Mass:
98.048g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
41.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.5
Literature
| Title | Journal |
|---|---|
| Hyperglycaemia-induced impairment of endothelium-dependent vasorelaxation in rat mesenteric arteries is mediated by intracellular methylglyoxal levels in a pathway dependent on oxidative stress. | Diabetologia 20100501 |
| Effects of 4-methylimidazole on cerebral glutamate decarboxylase activity and specific GABA receptor binding in mice. | Toxicology mechanisms and methods 20090301 |
| Methylglyoxal and methylglyoxal-arginine adducts do not directly inhibit endothelial nitric oxide synthase. | Annals of the New York Academy of Sciences 20080401 |
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