http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101102373-B1

Outgoing Links

Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F283-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F290-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08L67-03
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G63-91
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-3475
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-005
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08L75-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G61-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-05
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G61-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F290-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G63-91
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F283-00
filingDate 2009-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2012-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2012-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-101102373-B1
titleOfInvention Reactive benzotriazole-based UV absorbers and uses thereof
abstract The present invention relates to application and utilization to benzotriazoles having hydroxyl or carboxyl groups. Alkyl chain (R-CH 3 ) or methyl group (R-CH 3 ) attached to phenyl on the existing UV absorber benzotriazole [typically Tinuvin P, (2(2'-Hydroxy-5'-methyl-phenyl)benzotriazole] ) Is oxidized with an oxidizing agent to replace R-CH 2 OH and R-COOH to synthesize a reactive UV absorber Synthesized benzotriazole is particularly capable of participating in polyester polymerization in polymer polymerization by the presence of a reactive hydroxyl group. It is a monomer that can be attached to the terminal of the main chain, that is, it can also be called a high molecular weight reaction type stabilizer, an ultraviolet absorber with excellent performance to increase the molecular weight or to make a high molecular weight different from the hals system, or it has a hydroxyl group. It can be grafted with carboxyl groups, alcohols, isocyanates that are reactive with, and can achieve a better effect than binding to the main chain.n n n deleten n n delete
priorityDate 2009-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20040096558-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H11322841-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2003139499-A1
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421023647
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393636
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421932843
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID417430547
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13000698
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID466589071
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412753460
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID498427
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID17113
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397365
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419520409
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397482
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458397310
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394811
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID174
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8554
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419546729
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7489

Total number of triples: 42.