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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02F1-361
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02F1-355
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G02F1-35
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-74
filingDate 1997-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bb6578450c2490b6395686862a558d72
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9acacf891b55381b71424977cc2cdd5b
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_62b8dea5aa527df52ff4cc7d13f3c50d
publicationDate 1998-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H10195053-A
titleOfInvention Deuterated 2-adamantylamino-5-nitropyridine, organic nonlinear optical material containing the compound, and method for producing the compound
abstract PROBLEM TO BE SOLVED: To provide a deuterated 2-adamantylamino-5-nitropyridine (AANP) having a large wavelength conversion ratio in a wavelength conversion related to an optical communication wavelength region, particularly a wavelength around 1.55 μm, Provided is an organic nonlinear optical material for a device containing deuterated AANP. SOLUTION: Deuterated AANP is obtained by substituting deuterium for a hydrogen atom in an NH portion among hydrogen atoms constituting 2-adamantylamino-5-nitropyridine (AANP). An organic optical material is composed of the AANP containing the deuterated AANP. In this case, the content ratio is preferably 25% or more.
priorityDate 1996-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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