http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2005298576-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_7ef01e33058cf740cf2197991be97af1
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B25-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B67-10
filingDate 2004-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9bcd48636325f684092c6d9601975fa2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da0fd152363d96a1474d2d2604045a8c
publicationDate 2005-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2005298576-A
titleOfInvention Method for crystallizing quinophthalone compounds
abstract An object of the present invention is to provide a method for crystallizing a quinophthalone compound, which has a long-awaited size. In the method for crystallizing a quinophthalone compound represented by the general formula (1), a hydrocarbon solvent is used as a solvent, water and a dispersant are contained in the system, and the hydrocarbon solvent is distilled off to crystallize the crystal. A method characterized by analyzing. [Wherein, R 1 and R 2 are each independently a hydrogen atom, an alkyl group having 1 to 6 carbon atoms which may be substituted, —CONR 3 R 4, or —COOR 5 (R 3 to R 5 are each independently a hydrogen atom, carbon number 1 R6 and R7 each independently represents a hydrogen atom, or an optionally substituted alkyl group having 1 to 6 carbon atoms, which represents an optionally substituted alkyl group or an optionally substituted aryl group. . ] [Selection figure] None
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007197658-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2018135313-A
priorityDate 2004-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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