Indexing Metadata
Synthesis and Biological Activity of Some
Novel Phenyl Pyrazoline Derivatives |
DUBLIN | CORE | METADATA ITEM | METADATA FOR THIS DOCUMENT |
1 | Title | Title of Document | Synthesis and Biological Activity of Some
Novel Phenyl Pyrazoline Derivatives |
2 | Creator | Author's name, affiliation, country | SHAILESH H SHAH* and PANKAJ S PATEL *Department of Chemistry, Patel JBR Arts, Patel AMR Commerce & Patel JDKD Science College, Borsad & JJT-University, Rajasthan, India
Department of Chemistry, Sheth LH Science College, Mansa, India |
3 | Subject | Dicipline(s) | Chemical Science |
3 | Subject | Keywords | Chalcones, Phenyl pyrazolines, Azetidin-2-one, Antimicrobial activity |
4 | Description | Abstract | A new series of 4-(4-hydroxyphenyl)-3-chloro-1-{4-[5-(substituted phenyl)-1-phenyl- 4,5-dihydro-pyrazol-3-yl]phenyl}azetidin-2-one were synthesized by reacting 3-chloro-1-{4-[3-(substituted-phenyl)prop-2-enoyl]phenyl}-4-(4-hydroxyphenyl)azetidin-2-one (0.01 M) and phenyl hydrazine (0.01 M) in presence of acetic acid (glacial). All these compounds were characterized by means of their IR, 1H NMR, spectroscopic data and microanalysis. All the synthesized products were evaluated for their antimicrobial activity. All the compounds were tested for their antibacterial and antifungal activities by broth dilution method. |
5 | Publishers | Organizing agency, location | WWW Publications, India |
6 | Contributor | Sponsor(s) | - |
7 | Date | Date (YYYY-MM-DD) | - |
8 | Type | Status & genre | Peer-reviewed Article |
8 | Type | Type | |
9 | Formate | File Formate | PDF |
10 | Identifier | Uniform Resource Identifier | Click Here |
10 | Identifier | Digital Object Identifier | |
11 | Source | Journal/conference title; vol., no. (Year) | Chemical Science Transactions, Volume 1 , Number (3), (2012) |
12 | Lanuguage | English=en | en |
13 | Relation | Supp.files | |
14 | Coverage | | - |
15 | Copyright | Copyright and permissions | |
Chemical Science Transactions | Chem Sci Trans | CST | Online Chemistry Journal | Open Access
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