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| 1,3-Dimethyluracil Basic information |
Product Name: | 1,3-Dimethyluracil | Synonyms: | TIMTEC-BB SBB004164;3h)-pyrimidinedione,1,3-dimethyl-4(1h;N,N'-Dimethyluracil;N1,N3-Dimethyluracil;Uracil, 1,3-dimethyl-;1,3-dimethyl-2,4-pyrimidinedione;N-methyl-4-[(2-methyl-1,2,4-triazol-3-yl)azo]-N-(phenylmethyl)aniline;1,3-dimethylpyrimidine-2,4-dione | CAS: | 874-14-6 | MF: | C6H8N2O2 | MW: | 140.14 | EINECS: | 212-856-4 | Product Categories: | Pyridines, Pyrimidines, Purines and Pteredines;bc0001 | Mol File: | 874-14-6.mol | |
| 1,3-Dimethyluracil Chemical Properties |
| 1,3-Dimethyluracil Usage And Synthesis |
Chemical Properties | white to light yellow needles | Uses | 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. | Definition | ChEBI: 1,3-dimethyluracil is a pyrimidone that is uracil with methyl group substituents at positions 1 and 3. It has a role as a metabolite. It is functionally related to a uracil. | 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. | Purification Methods | Crystallise it from EtOH/ether. [Beilstein 24 III/IV 1196.] |
| 1,3-Dimethyluracil Preparation Products And Raw materials |
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