5-fluoro-1,3-dimethyluracil
5-fluoro-1,3-dimethyluracil structure
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Common Name | 5-fluoro-1,3-dimethyluracil | ||
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| CAS Number | 3013-92-1 | Molecular Weight | 158.13000 | |
| Density | 1.37g/cm3 | Boiling Point | 182.5ºC at 760mmHg | |
| Molecular Formula | C6H7FN2O2 | Melting Point | 132-134ºC(lit.) | |
| MSDS | Chinese USA | Flash Point | 64.1ºC | |
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Studies on oxidative modifications of nucleic acid pyrimidine bases.
Nucleic Acids Symp. Ser. (15) , 1-4, (1984) Oxidation of diacetylthymidine (4), triacetyluridine (5), and 5-fluoro-1,3-dimethyluracil (3) with m-chloroperbenzoic acid and cross-linkage of the bromohydrin (6) with the benzylamine and glycine ethyl ester are described. A Plausible mechanism for formation... |
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Development of diversified methods for chemical modification of the 5,6-double bond of uracil derivatives depending on active methylene compounds.
Molecules 17(6) , 6519-46, (2012) The reaction of 5-halogenouracil and uridine derivatives 1 and 7 with active methylene compounds under basic conditions produced diverse and selective C-C bond formation products by virtue of the nature of the carbanions. Three different types of reactions su... |
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Stereoselective synthesis of tetrahydronaphthocyclobuta[1,2-d]pyrimidinediones from 5-fluoro-1,3-dimethyluracil and naphthalenes.
Chem. Pharm. Bull. 53(2) , 258-9, (2005) Upon UV-irradiation in the presence of piperylene, 5-fluoro-1,3-dimethyluracil (5-FDMU) couples with naphthalenes having either an electron-withdrawing group or an electron-donating group by way of 1,2-cycloaddition via mode selectivity to give the correspond... |
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Structures of three photodimers of 5-fluoro-1,3-dimethyluracil:(I) an anti cyclobutene dimer, C12H13FN4O4;(II) the trans-anti cyclobutane dimer, C12H14F2N4O4; and (III) the cis-syn cyclobutane dimer, C12H14F2N4O4. Flippen-Anderson JL and Gilardi R.
Acta Crystallogr. C 40(11) , 1957-60, (1984)
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Enthalpy of formation of 5-fluoro-1,3-dimethyluracil: 5-Fluorouracil revisited. Amaral LMPF, et al.
J. Chem. Thermodyn. 75 , 106-115, (2014)
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Acid-Catalyzed Photosubstitution of 5-Fluoro-1,3-Dimethyluracil with Substituted Benzenes. Seki KI and Ohkura K.
Nucleosides Nucleotides 11(2-4) , 521-527, (1992)
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Synthesis of highly conjugated arylpropenylidene-1,3-diazin-2-ones via Paterno-Büchi reaction by photoreaction of 5-fluoro-1,3-dimethyluracil with 1-methoxynaphthalenes. Seki KI, et al.
Chem. Lett. 37(8) , 872-873, (2008)
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