Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/33243
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dc.contributor.authorPatil, A R-
dc.contributor.authorSunthankar, S V-
dc.date.accessioned2015-11-12T05:34:07Z-
dc.date.available2015-11-12T05:34:07Z-
dc.date.issued1980-03-
dc.identifier.issn0975-1025 (Online); 0971-0426 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/33243-
dc.description13-15en_US
dc.description.abstract2-Amino-8H-pyrazolo (4,5 -g) benzothiazole has been synthesized in high yield (90%) by the action of ammonium thiocyanate and bromine in glacial acetic acid on 6-aminoindazole. An angular structure, based on NMR and mass spectral data, has been assigned to the resulting heterocyclic amine. The amine was diazotized in phosphoric acid (87%) and coupled with various coupling components in acetic acid-ethanol cosolvent. The dyeing properties of the dyes obtained have been studied.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJFTR Vol.05(1) [March 1980]en_US
dc.titleDisperse Dyes: Part XIX-Synthesis of Disperse Azo Dyes from 2-Amino-8Hpyrazolo (4,5-g) benzothiazole and Their Dyeing Propertiesen_US
dc.typeArticleen_US
Appears in Collections:IJFTR Vol.05(1) [March 1980]

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