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Image of Sintesis Dan Uji Toksisitas Analog Pirazolin (E)-7-(4-Metoksibenziliden)-3-(4-Metoksifenil)-2-Fenil-3, 3a, 4, 5, 6, 7a-Heksahidro-2h-Pirazolo [4,3c] Piridin
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Sintesis Dan Uji Toksisitas Analog Pirazolin (E)-7-(4-Metoksibenziliden)-3-(4-Metoksifenil)-2-Fenil-3, 3a, 4, 5, 6, 7a-Heksahidro-2h-Pirazolo [4,3c] Piridin

FARIDA HANNUM HARAHAP / 1503123268 - Nama Orang;

Pyrazoline is five ring heterocyclic compounds with two adjacent nitrogen atoms which is known to have diverse biological activities such as antibacterial, antimalarial, antituberkular, anticancer and antioxidant. This study aims to synthesize derivatives of pyrazoline compounds to add variety and increase their bioactivity. Pyrazoline analogue (E)-7-(4-methoxybenzyliden)-3-(4-methoxyphenyl)-2-phenyl-3, 3a, 4, 5, 6, 7-hexahydro-2H- pyrazolo [4,3-c] piridine (FH-NHP-Pi) was synthesized of curcumin 5-bis ((E)-4-methoxybenzyliden) piperidine -4-on and phenylhydrazine using sodium hydroxide as catalyst. curcumin was prepared by condensing 4-piperidone monohydrate hydrochloride and 4-methoxybenzaldehide using NaOH as catalyst. Pyrozoline (FH-NHP-Pi) were synthesized via sealed vessel reactor with stirring speed 1000 rpm 80oC yield of 89,29 %. Purity of the compounds were analyzed using TLC, melting point, and HPLC. The structure of synthesized compounds were confirmed by UV, FTIR, NMR and HRMS spectroscopy studies. The toxicity of pyrazoline were evaluated by Brine Shrimp Lethality Test (BSLT) method. The result of the test showed pyrazoline (FH-NHP-Pi) is considered non-toxic were 217,77 µg/mL.
Keywords: curcumine, sealed vessel reactor, pyrazoline, toxicity


Ketersediaan
#
Perpustakaan Universitas Riau 03 02. 120 (0014)
03 02. 120 (0014)
Tersedia
Informasi Detail
Judul Seri
-
No. Panggil
03 02. 120 (0014)
Penerbit
Pekanbaru : Universitas Riau – FMIPA – Kimia., 2020
Deskripsi Fisik
xiii, 32 hlm.: ill.: 29 cm
Bahasa
Indonesia
ISBN/ISSN
-
Klasifikasi
03 02. 120 (0014)
Tipe Isi
-
Tipe Media
-
Tipe Pembawa
-
Edisi
-
Subjek
KIMIA
Info Detail Spesifik
-
Pernyataan Tanggungjawab
ELFITRA
Versi lain/terkait

Tidak tersedia versi lain

Lampiran Berkas
  • COVER, PENGESAHAN
  • KATA PENGANTAR, DAFTAR ISI
  • ABSTRAK
  • BAB I PENDAHULUAN
  • BAB II TINJAUAN PUSTAKA
  • BAB III METODOLOGI PENELITIAN
  • BAB IV HASIL DAN PEMBAHASAN
  • BAB V KESIMPULAN DAN SARAN
  • DAFTAR PUSTAKA
  • LAMPIRAN
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