Please use this identifier to cite or link to this item: https://repository.unej.ac.id/xmlui/handle/123456789/2700
Full metadata record
DC FieldValueLanguage
dc.contributor.authorIfada
dc.date.accessioned2013-12-03T02:50:39Z
dc.date.available2013-12-03T02:50:39Z
dc.date.issued2013-12-03
dc.identifier.nim082210101047
dc.identifier.urihttp://repository.unej.ac.id/handle/123456789/2700
dc.description.abstractA new compound from 5-fluorouracil (5-FU) derivatives, 1-(4- methoxybenzoyloxymethyl)-5-fluorouracil has been synthesized in a two steps reaction, alkylation (5-FU and formaldehyde to form 1-hydroxymethyl-5- fluorouracil) and esterification (1-hydroxymethyl-5-fluorouracil and 4- methoxybenzoylchloride to form 1-(4-methoxybenzoyloxymethyl)-5-fluorouracil). Reaction product purified by chromatography column, the product has been characteryzed for physical apperance is a yellowish white, crystal and melting range 168-169OC. Based on the FTIR and 1H-NMR spectra, it showed that the purified product does not contain a single compound. This fact is supported by Thin Layer Chromatography (TLC) result showing two spots for the pressure of 1-(4- methoxybenzoyloxymethyl)-5-fluorouracil and 4-methoxybenzoate acid.en_US
dc.relation.ispartofseries082210101047;
dc.subject5-fluorouracil derivates, anticancer, 1-(4-methoxybenzoyloxymethyl)-5- fluorouracil, benzoylationen_US
dc.titleSistensis 1-(4-Metoksibenzoiloksimetil)-5-Fluorourasil Sebagai Upaya Pengembagan Obat Antikankeren_US
dc.typeOtheren_US
Appears in Collections:UT-Faculty of Pharmacy

Files in This Item:
File Description SizeFormat 
Ifada - 082210101047_01.pdf671.24 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Admin Tools