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dc.contributor.authorNita Ernawati
dc.date.accessioned2013-12-17T02:25:27Z
dc.date.available2013-12-17T02:25:27Z
dc.date.issued2013-12-17
dc.identifier.nimNIM092210101097
dc.identifier.urihttp://repository.unej.ac.id/handle/123456789/9323
dc.description.abstractABSTRACT 5-fluorouracil is an antimetabolite class of anticancer agents that work induces apoptosis by inhibiting thymidilic acid biosynthesis. A novel 5-fluorouracil derivatives, 1-(4-trifluoromethylbenzoyloxymethyl)-5-fluorouracil were synthesized by two steps reaction. The first step is alkylation reaction between 5-fluorouracil, formaldehyde and aquadest to produce 1-hidroxymethyl-5-fluorouracil. The second step is benzoylation reaction between 1-hidroxymethyl-5-fluorouracil and 4trifluoromethylbenzoylchloride for 11 hours to produce the target compound. Target compound purified by column chromatography. Purified compound characterized and identified by 1 HNMR and FTIR KBr. Product compound form white needles crystal with melting range 172-174 o C. Spectra of 1 HNMR and FTIR KBr showed that pure 1-(4-trifluoromethylbenzoyloxymethyl)-5-fluorouracil was successfully synthesized.en_US
dc.language.isootheren_US
dc.relation.ispartofseries092210101097;
dc.subject5-fluorouracil 1-4-trifluoromethylbenzoyloxymethyl-5-fluorouracil alkylation anticancer benzoylationen_US
dc.titleSINTESIS 1-(4-TRIFLUOROMETILBENZOILOKSIMETIL)-5FLUOROURASIL SEBAGAI UPAYA PENGEMBANGAN OBAT ANTIKANKERen_US
dc.typeOtheren_US


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