<mets:mets OBJID="eprint_79616" LABEL="Eprints Item" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-3.xsd" xmlns:mets="http://www.loc.gov/METS/" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><mets:metsHdr CREATEDATE="2026-11-13T13:18:17Z"><mets:agent ROLE="CUSTODIAN" TYPE="ORGANIZATION"><mets:name>Institutional Repository UIN Sunan Kalijaga Yogyakarta</mets:name></mets:agent></mets:metsHdr><mets:dmdSec ID="DMD_eprint_79616_mods"><mets:mdWrap MDTYPE="MODS"><mets:xmlData><mods:titleInfo><mods:title>SINTESIS 5,7-DIHIDROKSI-4-METILKUMARIN MELALUI METODE MICROWAVE-ASSISTED PECHMANNN CONDENSATION SERTA UJI AKTIVITASNYA SEBAGAI ANTIBAKTERI TERHADAP STAPHYLOCOCCUS AUREUS DAN ESCHERICHIA COLI</mods:title></mods:titleInfo><mods:name type="personal"><mods:namePart type="given">NIM.: 22106030001</mods:namePart><mods:namePart type="family">Sukesi Diyah Tri Andini</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:abstract>Antibiotic resistance is a global health threat that drives the need for new antibacterial compounds. Coumarins and their derivatives, particularly 5,7-dihydroxy-4-methylcoumarin, have potential as antibacterial agents because they contain hydroxy (-OH) and methyl (-CH₃) groups that are believed to enhance interactions with bacterial cell targets. This study aims to synthesize 5,7-dihydroxy-4-methylcoumarin via a microwave-assisted Pechmann condensation under solvent-free conditions using FeCl₃ as a catalyst, characterize the structure of the synthesized compound, and test its antibacterial activity against Staphylococcus aureus and Escherichia coli.&#13;
The synthesis was carried out by reacting phloroglucinol and ethyl acetoacetate using microwave irradiation at a power of 300–450 W for 3 minutes. The product obtained was brownish-cream-colored needle-like crystals with a yield of 42.83% and a melting point of 282,8-283,3°C. Characterization using FTIR spectroscopy revealed characteristic absorptions of the phenolic O–H group (3433.20 cm⁻¹), the conjugated lactone C=O group (1667.96 cm⁻¹), and the aromatic C=C group (1553.77 cm⁻¹), while the ¹H-NMR spectrum showed hydroxyl proton signals at δ 10.242 and 10.468 ppm, aromatic proton signals at δ 6.210 and 6.122 ppm, an H-3 proton signal at δ 5.787 ppm, and a methyl proton signal at δ 2.432 ppm; the overall characterization results were consistent with the target structure.&#13;
The antibacterial activity test was conducted using the disk diffusion method with compound concentrations of 5%, 10%, 15%, and 20%, which showed weak activity against Staphylococcus aureus with an inhibition zone of 4.5 mm and moderate to weak activity against Escherichia coli with an inhibition zone of 6.5 mm. Based on the results of this study, the compound 5,7-dihydroxy-4-methylcoumarin has a 5% MIC value for each bacterium.</mods:abstract><mods:classification authority="lcc">543 Kimia Analitikal, Kimia Analisis</mods:classification><mods:originInfo><mods:dateIssued encoding="iso8061">2026-08-26</mods:dateIssued></mods:originInfo><mods:originInfo><mods:publisher>UIN SUNAN KALIJAGA YOGYAKARTA;FAKULTAS SAINS DAN TEKNOLOGI</mods:publisher></mods:originInfo><mods:genre>Thesis</mods:genre></mets:xmlData></mets:mdWrap></mets:dmdSec><mets:amdSec ID="TMD_eprint_79616"><mets:rightsMD ID="rights_eprint_79616_mods"><mets:mdWrap MDTYPE="MODS"><mets:xmlData><mods:useAndReproduction>
<p xmlns="http://www.w3.org/1999/xhtml"><strong>For work being deposited by its own author:</strong> 
In self-archiving this collection of files and associated bibliographic 
metadata, I grant Institutional Repository UIN Sunan Kalijaga Yogyakarta the right to store 
them and to make them permanently available publicly for free on-line. 
I declare that this material is my own intellectual property and I 
understand that Institutional Repository UIN Sunan Kalijaga Yogyakarta does not assume any 
responsibility if there is any breach of copyright in distributing these 
files or metadata. (All authors are urged to prominently assert their 
copyright on the title page of their work.)</p>

<p xmlns="http://www.w3.org/1999/xhtml"><strong>For work being deposited by someone other than its 
author:</strong> I hereby declare that the collection of files and 
associated bibliographic metadata that I am archiving at 
Institutional Repository UIN Sunan Kalijaga Yogyakarta) is in the public domain. If this is 
not the case, I accept full responsibility for any breach of copyright 
that distributing these files or metadata may entail.</p>

<p xmlns="http://www.w3.org/1999/xhtml">Clicking on the deposit button indicates your agreement to these 
terms.</p>
    </mods:useAndReproduction></mets:xmlData></mets:mdWrap></mets:rightsMD></mets:amdSec><mets:fileSec><mets:fileGrp USE="reference"><mets:file ID="eprint_79616_1087703_1" SIZE="6411305" OWNERID="https://digilib.uin-suka.ac.id/id/eprint/79616/1/22106030001_BAB-I_IV-atau-V_DAFTAR-PUSTAKA.pdf" MIMETYPE="application/pdf"><mets:FLocat LOCTYPE="URL" xlink:type="simple" xlink:href="https://digilib.uin-suka.ac.id/id/eprint/79616/1/22106030001_BAB-I_IV-atau-V_DAFTAR-PUSTAKA.pdf"></mets:FLocat></mets:file></mets:fileGrp><mets:fileGrp USE="reference"><mets:file ID="eprint_79616_1087704_1" SIZE="9731671" OWNERID="https://digilib.uin-suka.ac.id/id/eprint/79616/2/22106030001_BAB-II_sampai_SEBELUM-BAB-TERAKHIR.pdf" MIMETYPE="application/pdf"><mets:FLocat LOCTYPE="URL" xlink:type="simple" xlink:href="https://digilib.uin-suka.ac.id/id/eprint/79616/2/22106030001_BAB-II_sampai_SEBELUM-BAB-TERAKHIR.pdf"></mets:FLocat></mets:file></mets:fileGrp></mets:fileSec><mets:structMap><mets:div DMDID="DMD_eprint_79616_mods" ADMID="TMD_eprint_79616"><mets:fptr FILEID="eprint_79616_document_1087703_1"></mets:fptr><mets:fptr FILEID="eprint_79616_document_1087704_1"></mets:fptr></mets:div></mets:structMap></mets:mets>