http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-102468876-B1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02E10-549
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K10-484
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K85-657
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K85-111
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D517-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D513-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D517-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D513-04
filingDate 2017-10-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2022-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-102468876-B1
titleOfInvention Naphthobischalcogenadiazole derivatives and methods for their preparation
abstract An object of the present invention is to provide a naphthobischalcogenadiazole derivative that can be used as an intermediate for producing a fluorine atom-introduced naphthobischalcogenadiazole compound. The naphthobischalcogenadiazole derivatives of the present invention are of the formula (I): (Wherein, A 1 and A 2 are each independently an oxygen atom, a sulfur atom, a selenium atom or a tellurium atom; X 1 and X 2 are each independently a hydrogen atom, a halogen atom, a boronic acid group, a boronic acid ester group, boronic acid diamino naphthalenamide group, boronic acid N-methyliminodiacetic acid ester group, trifluoroborate base or triol borate base).
priorityDate 2016-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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