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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12
filingDate 1993-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7fd59c2b87d0513cab5160da6a6ea612
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5729ddd419921ada85feeaba8a8b517e
publicationDate 1996-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SK-278131-B6
titleOfInvention 3-(2-alkylthio-6-benzothiazolylaminomethyl)-2-benzoxazolinthiones and method of their preparation
abstract There were prepared 3-(2-alkylthio-6- -benzothiazolylaminomethyl)-2-benzoxazolinethiones of general formula I, where alkyl means cyclopentyl, alkyl, benzyl, or saturated chain with 2 to 8 atoms of carbon. Synthesis of these compounds is realized by reaction of 3-hydroxymethyl-2- -benzoxazolinthione with 2-alkylthio-6- aminobenzothiazols in ethanol at the boiling point. Compounds are antialgal effective.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AU-2004223827-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004085425-A1
priorityDate 1993-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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