Synthesis, modification, characterization and biological activity of 3-hydroxybenzaldehydesalicylhydrazide [Sintesis, modifikasi, pencirian dan aktiviti biologi 3-hidroksibenzaldehidesalisilhidrazida]

A series of hydrazone Schiff base (compounds S, S8, S10 and S12) were synthesized by condensation reaction of salicylhydrazide with 3-hydroxybenzaldehyde, 3-(octyloxy)benzaldehyde, 3-(decyloxy)benzaldehyde and 3-(dodecyloxy) benzaldehyde, respectively. Herein, the addition of alkane numbers are repo...

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Main Authors: Nornadia, Jasin, Meng, Guan Tay, Hashimatul Fatma, Hashim
Format: Article
Language:English
Published: Malaysian Society of Analytical Sciences 2017
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Online Access:http://ir.unimas.my/id/eprint/18936/7/SYNTHESIS.pdf
http://ir.unimas.my/id/eprint/18936/
http://www.ukm.my/mjas/mjas2018/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85032027821&doi=10.17576%2fmjas-2017-2105-24&partnerID=40&md5=e7bdfc217e5a78ba945222607aca97df
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spelling my.unimas.ir.189362022-06-22T03:24:16Z http://ir.unimas.my/id/eprint/18936/ Synthesis, modification, characterization and biological activity of 3-hydroxybenzaldehydesalicylhydrazide [Sintesis, modifikasi, pencirian dan aktiviti biologi 3-hidroksibenzaldehidesalisilhidrazida] Nornadia, Jasin Meng, Guan Tay Hashimatul Fatma, Hashim QD Chemistry A series of hydrazone Schiff base (compounds S, S8, S10 and S12) were synthesized by condensation reaction of salicylhydrazide with 3-hydroxybenzaldehyde, 3-(octyloxy)benzaldehyde, 3-(decyloxy)benzaldehyde and 3-(dodecyloxy) benzaldehyde, respectively. Herein, the addition of alkane numbers are reported using suscessful Williamson etherification method by reacting 3-hydroxybenzaldehyde with bromooctane, bromodecane and bromododecane, respectively. All compounds were characterised using Fourier Transform Infrared and 1H Nuclear Mangnetic Resonance spectroscopic. The compounds were assayed to antibacterial activity against Gram-positive and Gram-negative bacteria using Bacillus cereus and Escherichia coli by disc diffusion method. Interestingly, among the compounds tested S8 showed a strong inhibition against Escherichia coli and none of the compounds tested show significant result against Bacillus cereus. Malaysian Society of Analytical Sciences 2017-10 Article PeerReviewed text en http://ir.unimas.my/id/eprint/18936/7/SYNTHESIS.pdf Nornadia, Jasin and Meng, Guan Tay and Hashimatul Fatma, Hashim (2017) Synthesis, modification, characterization and biological activity of 3-hydroxybenzaldehydesalicylhydrazide [Sintesis, modifikasi, pencirian dan aktiviti biologi 3-hidroksibenzaldehidesalisilhidrazida]. Malaysian Journal of Analytical Sciences, 21 (5). pp. 1195-1202. ISSN 1394-2506 http://www.ukm.my/mjas/mjas2018/ https://www.scopus.com/inward/record.uri?eid=2-s2.0-85032027821&doi=10.17576%2fmjas-2017-2105-24&partnerID=40&md5=e7bdfc217e5a78ba945222607aca97df
institution Universiti Malaysia Sarawak
building Centre for Academic Information Services (CAIS)
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sarawak
content_source UNIMAS Institutional Repository
url_provider http://ir.unimas.my/
language English
topic QD Chemistry
spellingShingle QD Chemistry
Nornadia, Jasin
Meng, Guan Tay
Hashimatul Fatma, Hashim
Synthesis, modification, characterization and biological activity of 3-hydroxybenzaldehydesalicylhydrazide [Sintesis, modifikasi, pencirian dan aktiviti biologi 3-hidroksibenzaldehidesalisilhidrazida]
description A series of hydrazone Schiff base (compounds S, S8, S10 and S12) were synthesized by condensation reaction of salicylhydrazide with 3-hydroxybenzaldehyde, 3-(octyloxy)benzaldehyde, 3-(decyloxy)benzaldehyde and 3-(dodecyloxy) benzaldehyde, respectively. Herein, the addition of alkane numbers are reported using suscessful Williamson etherification method by reacting 3-hydroxybenzaldehyde with bromooctane, bromodecane and bromododecane, respectively. All compounds were characterised using Fourier Transform Infrared and 1H Nuclear Mangnetic Resonance spectroscopic. The compounds were assayed to antibacterial activity against Gram-positive and Gram-negative bacteria using Bacillus cereus and Escherichia coli by disc diffusion method. Interestingly, among the compounds tested S8 showed a strong inhibition against Escherichia coli and none of the compounds tested show significant result against Bacillus cereus.
format Article
author Nornadia, Jasin
Meng, Guan Tay
Hashimatul Fatma, Hashim
author_facet Nornadia, Jasin
Meng, Guan Tay
Hashimatul Fatma, Hashim
author_sort Nornadia, Jasin
title Synthesis, modification, characterization and biological activity of 3-hydroxybenzaldehydesalicylhydrazide [Sintesis, modifikasi, pencirian dan aktiviti biologi 3-hidroksibenzaldehidesalisilhidrazida]
title_short Synthesis, modification, characterization and biological activity of 3-hydroxybenzaldehydesalicylhydrazide [Sintesis, modifikasi, pencirian dan aktiviti biologi 3-hidroksibenzaldehidesalisilhidrazida]
title_full Synthesis, modification, characterization and biological activity of 3-hydroxybenzaldehydesalicylhydrazide [Sintesis, modifikasi, pencirian dan aktiviti biologi 3-hidroksibenzaldehidesalisilhidrazida]
title_fullStr Synthesis, modification, characterization and biological activity of 3-hydroxybenzaldehydesalicylhydrazide [Sintesis, modifikasi, pencirian dan aktiviti biologi 3-hidroksibenzaldehidesalisilhidrazida]
title_full_unstemmed Synthesis, modification, characterization and biological activity of 3-hydroxybenzaldehydesalicylhydrazide [Sintesis, modifikasi, pencirian dan aktiviti biologi 3-hidroksibenzaldehidesalisilhidrazida]
title_sort synthesis, modification, characterization and biological activity of 3-hydroxybenzaldehydesalicylhydrazide [sintesis, modifikasi, pencirian dan aktiviti biologi 3-hidroksibenzaldehidesalisilhidrazida]
publisher Malaysian Society of Analytical Sciences
publishDate 2017
url http://ir.unimas.my/id/eprint/18936/7/SYNTHESIS.pdf
http://ir.unimas.my/id/eprint/18936/
http://www.ukm.my/mjas/mjas2018/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85032027821&doi=10.17576%2fmjas-2017-2105-24&partnerID=40&md5=e7bdfc217e5a78ba945222607aca97df
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score 13.160551