http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106117230-B

Outgoing Links

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K2211-1029
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K2211-1088
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N21-6428
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K11-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-107
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-107
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K11-06
filingDate 2016-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2018-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2018-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-106117230-B
titleOfInvention Replace rhodamine B amide groups Thiourea fluorescent probe compounds and its preparation method and application
abstract The invention discloses a kind of substitution rhodamine B amide groups Thiourea fluorescent probe compounds and its preparation method and application, belong to the synthesis technical field of fluorescent probe compounds.Technical scheme of the present invention main points are:Replace rhodamine B amide groups Thiourea fluorescent probe compounds, chemical structural formula is: , wherein R is Cl, OMe or CF 3 .The invention also discloses the preparation method of the substitution rhodamine B amide groups Thiourea fluorescent probe compounds and its as the application in detection metal mercury ions organic molecule fluorescence probe.The fluorescent probe compounds of the present invention show preferable antijamming capability, can relatively accurately detect trace heavy metal mercury ion, and selective and sensitivity is preferable.
priorityDate 2016-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 41.