| Weight | 140.142 g/mol |
|---|---|
| Formula | C6H8N2O2 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
1,3-Dimethyluracil (874-14-6)
Score:
#1873 in Biochemistry
,
#5072 in Chemistry
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- Nucleosides. 121. Improved and general synthesis of 2-deoxy C-nucleosides. Synthesis of 5-(2-deoxy--D-erythro-pentofuranosyl)uracil, -1-methyluracil, -1,3-dimethyluracil, and -isocytosine (Journal of Organic Chemistry, 1982)
- The SO4(.-)-induced chain reaction of 1,3-dimethyluracil with peroxodisulphate. (International Journal of Radiation Biology, 1987)
- Infrared study of hydrogen-bonded complexes involving phenol derivatives and polyfunctional bases. II: 3-Methyl-4-pyrimidone, 1-methyl-2-pyrimidone, 1,4,4-trimethylcytosine, and 1,3-dimethyluracil (The Journal of Physical Chemistry, 1984)
- ULTRAVIOLET IRRADIATION OF PYRIMIDINE DERIVATIVES: I. 1,3-DIMETHYLURACIL (Canadian Journal of Chemistry, 1957)
- Matrix isolation studies of nucleic acid constituentsIII. 1-Methyluracil, 3-methyluracil and 1,3-dimethyluracil monomers (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 1985)
- Palladium-catalyzed direct 5-arylation of 1,3-dimethyluracil with aryl bromides: an electrophilic metalationdeprotonation with electrophilic arylpalladium intermediate (Tetrahedron Letters, 2011)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN1C=CC(=O)N(C1=O)C
-
InChIKeyJSDBKAHWADVXFU-UHFFFAOYSA-N
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