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http://nopr.niscpr.res.in/handle/123456789/6445Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Sareen, Vineeta | - |
| dc.contributor.author | Khatri, Vineeta | - |
| dc.contributor.author | Jain, Prakash | - |
| dc.contributor.author | Sharma, Kanti | - |
| dc.date.accessioned | 2009-11-05T06:40:49Z | - |
| dc.date.available | 2009-11-05T06:40:49Z | - |
| dc.date.issued | 2006-05 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/6445 | - |
| dc.description | 1288-1290 | en_US |
| dc.description.abstract | 2,4,6-Trichloro-1,3,5-triazine has been reacted selectively with nucleophilic reagents, 6-Fluoro-2-aminobenzothiazole 1, phenyl thioureas 2 and different substituted thioureas 3 to give 2-(6-fluorobenzothiazole-2'-ylamino)-4-(phenylthioureido)-6-(substituted thioureido)-1,3,5-triazine 4. These compounds are evaluated for their antimicrobial activity. The structure of all these compounds have been confirmed by IR, 1H NMR, mass spectral data and elemental analysis. Benzothiazoles, s-triazenes and thioureas exhibit various biological activities. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.relation.ispartofseries | Int.Cl.8 C 07 D | en_US |
| dc.source | IJC-B Vol.45B(05) [May 2006] | en_US |
| dc.subject | Fluorobenzothiazole | en_US |
| dc.subject | triazine derivatives | en_US |
| dc.subject | antimicrobial activity | en_US |
| dc.subject | antifungal activity | en_US |
| dc.subject | phenyl thioureas | en_US |
| dc.subject | antimicrobial and antifungal activity | en_US |
| dc.title | Synthesis of 2-(6-fluorobenzothiazole-2'-ylamino)-4-(phenylthioureido)-6-(substituted thioureido)-1,3,5-triazine as antimicrobial agent | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.45B(05) [May 2006] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 45B(5) 1288-1290.pdf | 39.86 kB | Adobe PDF | View/Open |
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