alexa Abstract | Studies on some organic molecules containing ligand and sulfa drug moieties

Journal of Chemical and Pharmaceutical Research
Open Access

OMICS International organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

Open Access Journals gaining more Readers and Citations

700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)

Original Articles Open Access

Abstract

The condensation reaction between 4-(((5-(ethoxycarbonyl)furan-2-yl)methyl)(methyl)amino)-2-hydroxybenzoic acid and Sulphanilamide was give 2-hydroxy-4-(methyl((5-(4-sulfamoylphenylcarbamoyl)furan-2-yl)methyl)amino) benzoic acid (HMSPCFMAB). The novel ligand was characterized by elemental analysis and spectral studies. The transition metal chelates viz. Cu2+, Ni2+ , Co2+ , Mn2+ and Zn2+ of HMSPCFMAB were prepared and characterized by metal-ligand (M:L) ratio, IR and reflectance spectroscopes and magnetic properties. The antifungal activity of HMSPCFMAB and its metal chelates was examined against various fungi.

To read the full article Peer-reviewed Article PDF image

Author(s): Sefali S Patel Harshadkumar P Patel and Asha D Patel

Keywords

4-(((5-(ethoxycarbonyl)furan-2-yl)methyl)(methyl)amino)-2-hydroxybenzoic acid, Sulphanilamide, Magnetic moment, Spectroscopies study and Antifungal properties., organic molecules

 
Peer Reviewed Journals
 
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
 
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

 
© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version
adwords