http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0001560-A2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-3442
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D245-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D243-12
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filingDate 1978-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f0e98a952279ca3bb16d764bd1dd8f2b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b2709dca9b4e18ba059ae2fb6b0c48bf
publicationDate 1979-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0001560-A2
titleOfInvention UV-light-stabilized compositions containing substituted 1,5-diazacycloalkanes and 2-keto-1,5-diazacycloalkanes, novel compounds and synthesis thereof
abstract Novel polysubstituted 1,5-diazacycloalkanes and polysubstituted 2-keto-1,5- diazcycloalkanes are powerful stabilizers for materials subject to ultraviolet (UV) light degradation, particularly for polyolefins. The cyclic compounds of this invention have (a) a fixed three-carbon bridge between the N' and N<sup>5</sup> atoms of the diaza ring, the remaining portion of the ring having a variable length bridge of two or more carbon stoms, (b) an N-adjacent carbon atom of the diaza ring is polysubstituted, that is, has two substituents which may be cyclizable.Compositions containing (a) the polysubstituted 1,5-diazacycloalkanes and polysubstituted 2-keto-1,5- diazacycloalkanes of this invention, and (b) prior art polysubstituted 1,5-diazacycloalkanes and polysubstituted 2-keto-1,5-diazscycloalkanes, exhibit excellent stability to UV light.A novel synthesis for preparing polysubstituted 2- keto-1,5- diazacycloalkanes is disclosed.
priorityDate 1977-09-21-04:00^^<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: 475.