http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1300402-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5ddadb999be4f451dfc44d8e359d8f6a |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C217-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N33-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61L2-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-096 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-185 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P31-02 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61L2-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-185 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N33-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C217-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-096 |
| filingDate | 2002-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4a81f37d432fac3bf562de7f8483461 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b95e6d3e44be80eb1ab8f51d2478ddae http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b1133e4f7f2bbaabe6a35c4729235be |
| publicationDate | 2003-04-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-1300402-A1 |
| titleOfInvention | Alkoxybenzylamines with antimicrobial properties |
| abstract | R 1 und R 2 unabhängig voneinander Wasserstoff, nicht substituiertes oder mit einem odernmehreren Hydroxy, Halogen, C 1 -C 18 -Alkyl, C 1 -C 18 -Alkoxy oder Amino substituiertes C 1 -C 20 -Alkyl,nC 2 -C 20 -Alkenyl, C 2 -C 20 -Alkinyl, C 3 -C 12 -Cycloalkyl, C 3 -C 7 -Cycloalkyl-C 1 -C 20 -Alkyl, C 1 -C 6 -Alkoxy-C 1 -C 20 -Alkyl,nC 1 -C 12 -Alkyl-oxycarbonyl, Phenyl, Phenyl-C 1 -C 20 -Alkyl; Carboxy; odernPyridino-C 1 -C 5 -alkyl; oder R 1 und R 2 zusammen mit dem sie verbindenden Stickstoffatom einen 5- bis 7-gliedrigennmonocyclischen heterocyclischen Ring bilden; R 3 und R 4 unabhängig voneinander nicht substituiertes oder mit einem oder mehrerennHydroxy, Halogen, C 1 -C 18 -Alkyl, C 1 -C 18 -Alkoxy, oder Amino substituiertes C 1 -C 20 -Alkyl;nund n 0 oder 1; nbedeuten.Alkoxybenzylamines of the formula are described wherein R 1 and R 2 independently of one another hydrogen, unsubstituted or substituted by one or more hydroxy, halogen, C 1 -C 18 alkyl, C 1 -C 18 alkoxy or amino C 1 -C 20 alkyl, C 2 -C 20 alkenyl, C 2 -C 20 alkynyl, C 3 -C 12 cycloalkyl, C 3 -C 7 cycloalkyl-C 1 -C 20 alkyl, C 1 -C 6 alkoxy-C 1 -C 20 alkyl, C 1 - C 12 alkyl oxycarbonyl, phenyl, phenyl C 1 -C 20 alkyl; carboxy; or pyridino-C 1 -C 5 alkyl; or R 1 and R 2 together with the nitrogen atom connecting them form a 5- to 7-membered monocyclic heterocyclic ring; R 3 and R 4 independently of one another unsubstituted or with one or more hydroxy, halogen, C 1 -C 18 alkyl, C 1 -C 18 alkoxy, or amino-substituted C 1 -C 20 alkyl; and n 0 or 1; mean.n n n They are suitable for the antimicrobial treatment of surfaces, as an antimicrobialnActive substance against gram-positive and gram-negative bacteria. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2006133784-A1 |
| priorityDate | 2001-10-04-04:00^^<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: 175.