http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0061798-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-653 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-653 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D521-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-06 |
| filingDate | 1982-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1986-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1986-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0061798-B1 |
| titleOfInvention | Novel antimicrobial triazole derivatives |
| abstract | A compound selected from the group consisting of a 2 min -amino-2 min -phenyl-ethyl-1H-1,2,4-triazole of the formula (I) <CHEM> and the phytopharmaceutically acceptable salts and metal complexes thereof, wherein: R1 is a member selected from the group consisting of hydrogen, halo, C1-C4-alkyl, C1-C4-alkyloxy, and C1-C2-haloalkyl; R2 is a member selected from the group consisting of hydrogen, halo, C1-C4-alkyl, C1-C4-alkyloxy, C1-C2-haloalkyl and phenyl; R3 is a member selected from the group consisting of hydrogen, C1-C12-alkyl, C3-C8-cycloalkyl which is optionally substituted with C1-C4-alkyl, and aralkyl with maximum 2 carbon atoms in the alkyl part and optionally substituted on the phenyl nucleus with halo or nitro; R4 is a member selected from the group consisting of hydrogen and C1-C4-alkyl; whereby R3 and R4 may, together with the nitrogen atom to which they are attached, form a 3- to 7-membered saturated heterocyclic ring which may optionally be interrupted by oxygen, sulfur or NR5 and optionally substituted with R6, wherein R5 and R6 are each independently C1-C4-alkyl, a method of combating microorganisms by the use of such compounds, microbicidal agents comprising such compounds as active ingredients, processes of preparing the subject compounds and intermediates used therefore. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104370835-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7459474-B2 |
| priorityDate | 1981-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 66.