Digilib Perpustakaan Universitas Riau

  • Beranda
  • Informasi
  • Berita
  • Bantuan
  • Pustakawan
  • Pilih Bahasa :
    Bahasa Arab Bahasa Bengal Bahasa Brazil Portugis Bahasa Inggris Bahasa Spanyol Bahasa Jerman Bahasa Indonesia Bahasa Jepang Bahasa Melayu Bahasa Persia Bahasa Rusia Bahasa Thailand Bahasa Turki Bahasa Urdu

Pencarian berdasarkan :

SEMUA Pengarang Subjek ISBN/ISSN Pencarian Spesifik

Pencarian terakhir:

{{tmpObj[k].text}}
Image of Sintesis Senyawa Konjugasi Kalkon (E)-1-(4-((3-(1-(7-Klorokuinolin-4-Il)Triaz-2-En-1-Il)Prop-2-Un-1-Il)Oksi)-2-Hidroksifenil)-3(Metoksifenil)Prop-2-En-1-On
Penanda Bagikan

CD Skripsi

Sintesis Senyawa Konjugasi Kalkon (E)-1-(4-((3-(1-(7-Klorokuinolin-4-Il)Triaz-2-En-1-Il)Prop-2-Un-1-Il)Oksi)-2-Hidroksifenil)-3(Metoksifenil)Prop-2-En-1-On

RAHMAD SETIAWAN RABBY / 1603115869 - Nama Orang;

SUMMARY
Organic synthesis has now developed into one of the most important aspects and the main driving force of organic chemistry. With synthesis, natural products can be produced on a large scale in an easy and low-cost way. Through the isolation of natural materials in the modern era and technological advances today, it is possible to synthesize new medicinal compounds based on structural modifications of previously discovered medicinal compounds through the isolation of natural materials. One of them is the synthesis of chalcone compounds (E)-1-(4-((1-(7-chloroquinoline-4-yl)-1H-1,2,3-triazole-4-yl)methoxy) -2-hydroxy phenyl)-3-(4-methoxyphenyl)prop-2-en-1-one via chalcone modification by incorporating a chloroquinoline group with a triazole linker molecule. Synthesis was carried out convergently through the formation of chloroquinoline azides and the formation of propargyl substituted chalcones. These two compounds were then combined through the formation of a linking compound, namely triazole, which was carried out by "click chemistry". The yield obtained from the chalcone synthesis was 28.90 %. The low yield is because the synthesized compound is an intermediate product, which is a minor product. The interpretation results of UV, FTIR, 1H-NMR, 13C-NMR and HR-MS data indicated that the synthesized compound was (E)-1-(4-((3-(1-(7-chloroquinoline-4-yl)triaz-2-en-1-yl))prop-2-un-1-yl)oxy)-2-hydroxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one. This compound is an intermediate compound of the target molecule.


Ketersediaan
#
Perpustakaan Universitas Riau 1603115869
1603115869
Tersedia
Informasi Detail
Judul Seri
-
No. Panggil
1603115869
Penerbit
Pekanbaru : Universitas Riau - FMIPA - KIMIA., 2023
Deskripsi Fisik
-
Bahasa
Indonesia
ISBN/ISSN
-
Klasifikasi
1603115869
Tipe Isi
-
Tipe Media
-
Tipe Pembawa
-
Edisi
-
Subjek
KIMIA
Info Detail Spesifik
-
Pernyataan Tanggungjawab
tethi
Versi lain/terkait

Tidak tersedia versi lain

Lampiran Berkas
  • JUDUL
  • DAFTAR ISI
  • ABSTRAK
  • BAB I PENDAHULUAN
  • BAB II TINJAUAN PUSTAKA
  • BAB III METODE PENELITIAN
  • BAB IV HASIL DAN PEMBAHASAN
  • B
  • BAB V KESIMPULAN DAN SARAN
  • DAFTAR PUSTAKA
  • LAMPIRAN
Komentar

Anda harus masuk sebelum memberikan komentar

Digilib Perpustakaan Universitas Riau
  • Informasi
  • Layanan
  • Pustakawan
  • Area Anggota

Tentang Kami

As a complete Library Management System, SLiMS (Senayan Library Management System) has many features that will help libraries and librarians to do their job easily and quickly. Follow this link to show some features provided by SLiMS.

Cari

masukkan satu atau lebih kata kunci dari judul, pengarang, atau subjek

Donasi untuk SLiMS Kontribusi untuk SLiMS?

© 2026 — Senayan Developer Community

Ditenagai oleh SLiMS
Pilih subjek yang menarik bagi Anda
  • Karya Umum
  • Filsafat
  • Agama
  • Ilmu-ilmu Sosial
  • Bahasa
  • Ilmu-ilmu Murni
  • Ilmu-ilmu Terapan
  • Kesenian, Hiburan, dan Olahraga
  • Kesusastraan
  • Geografi dan Sejarah
Icons made by Freepik from www.flaticon.com
Pencarian Spesifik
Kemana ingin Anda bagikan?