Quality Level
assay
99%
form
powder
mp
119-122 °C (lit.)
SMILES string
CN1C=CC(=O)N(C)C1=O
InChI
1S/C6H8N2O2/c1-7-4-3-5(9)8(2)6(7)10/h3-4H,1-2H3
InChI key
JSDBKAHWADVXFU-UHFFFAOYSA-N
General description
1,3-Dimethyluracil is a pyrimidine derivative. Stability of the C6-centered carbanions derived from 1,3-dimethyluracil has been investigated in the gas phase and in DMSO and water solutions. The excited state structural dynamics of 1,3-dimethyluracil (DMU) in water and acetonitrile has been studied by resonance Raman spectroscopy. Crystal structure of 1,3-dimethyluracil has been reported. Ultraviolet irradiation of aqueous 1,3-dimethyluracil results in hydration of the 5:6 double bond of the uracil ring to form 1,3-dimethyl-6-oxy-hydrouracil.
Application
1,3-Dimethyluracil is suitable reagent used to investigate the steady-state absorption and fluorescence spectra of uracil derivatives. It may be used in the preparation of 2,6-dihydroxynicotinamide.
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
K Seki et al.
Nucleic acids symposium series, (29)(29), 43-44 (1993-01-01)
In order to obtain insight into the protonation of the electron adducts of pyrimidine bases (I) and the chemical behavior of the resulting radicals under an acidic condition, the photoreaction of 5-substituted 1,3-dimethyluracil (1) (substituents; p-xylyl, methyl, H, Cl, and
Ultraviolet irradiation of pyrimidine derivatives: I. 1, 3-dimethyluracil.
Moore AM and Thomson CH.
Canadian Journal of Chemistry, 35(2), 163-169 (1957)
T Itahara et al.
Nucleic acids symposium series, (16)(16), 61-64 (1985-01-01)
Reaction with peroxodisulfate ion was investigated, that is, reaction of 1,3-dimethyluracil, 1,3-dimethylthymine, and caffeine with carbon radicals formed from decarboxylation of carboxylic acids, oxidation of the methyl group at 5-position of thymines, and halogenation of nucleic acids bases and their
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| 货号 | GTIN |
|---|---|
| 349801-5G | 04061831234305 |