Description
A pyrimidone that is uracil with a methyl group substituent at position 1.
Chemical properties
| Chemical formula | Net charge | Average mass |
|---|---|---|
| C5H6N2O2 | 0 | 126.11330 |
Nomenclature
| IUPAC | SMILES | InChI | InChIKey |
|---|---|---|---|
| 1-methylpyrimidine-2,4(1H,3H)-dione | Cn1ccc(=O)[nH]c1=O | InChI=1S/C5H6N2O2/c1-7-3-2-4(8)6-5(7)9/h2-3H,1H3,(H,6,8,9) | XBCXJKGHPABGSD-UHFFFAOYSA-N |
Citations
- Kawahara, S, et al. 2003. Evaluation of the hydrogen bond energy of base pairs formed between substituted 9-methyladenine derivatives and 1-methyluracil by use of molecular orbital theory. Nucleic Acids Symposium Series. (44).
- Kolosov, AI, et al. 1975. [The antiblastomatous activity of 9-methyladenine, 1-methyluracil and 1-methylthymine]. Voprosy Onkologii. 21(5).
- McMullan, RK, et al. 1989. Crystal structure of 1-methyluracil from neutron diffraction at 15, 60 and 123 K. Acta Crystallographica. Section B, Structural Science. 45 ( Pt 3).
- van der Wijst, T, et al. 2008. Rare tautomers of 1-methyluracil and 1-methylthymine: tuning relative stabilities through coordination to PtII complexes. Chemistry (Weinheim An Der Bergstrasse, Germany). 15(1).