http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0016571-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c9cd29e9f3b494af33cdc2e51b010135
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-36
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-48
filingDate 1980-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dafd6611c6047cdbe0d1231ac8282ec0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_602b47a0db62e50fcd8f2e81d5a357a0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4365c148f27c7617780b8888b291dabe
publicationDate 1980-10-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0016571-A1
titleOfInvention N-(Arylthiocarbamoyl)-2-amino-1H-isoindole-1,3-(2H)diones, processes for their preparation and their use as plant growth regulators
abstract A novel class of N-(arylthiocarbamoyl)-2- amino-1H-isoindole-1,3-(2H) diones which are useful as plant growth regulators have the general structural formula:n in whichn R 1 is; C 1 to C 4 alkyl, nitro or halo and n is zero or an integer from 1 to 4 R 2 and R 3 are; H or C to C. alkyl, or benzyl and Ar is; adamantyl, C 3 to C 4 alkyl or alkenyl, benzyl, halobenzyl, naphthyl, phenyl or phenyl bearing thereon from one to three of the substituents: cyano, benzyloxy, nitro, bromo, chloro, trifluoromethyl and C 1 to C 4 alkyl, alkenyl, alkoxy, alkylthio and alkyl-substituted amino.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0030789-A3
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0241863-A3
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0241863-A2
priorityDate 1979-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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