http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0144420-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N57-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-3808 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-4006 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N57-20 |
| filingDate | 1984-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1987-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1987-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0144420-B1 |
| titleOfInvention | Guanidated aminophosphonic acid compounds |
| abstract | Novel guanidated aminophosphonic acid compounds their use as biocides and their intermediates. The compounds are guanidated N-(aminoalkyl) aminoalkanephosphonic acid derivatives and are characterized in that they comprise both a phosphonic acid type group and at least one guanidino group and also in that they are based on alkylene amines. The compounds have the general formula: (I) wherein Z and Z' are hydrogen, a lower alkyl group or an alkali metal, Y is hydrogen or an amidine group, m is 1-3, n is 4-16 and p is 1-3. The compounds can be prepared by reacting a halogenoalkanephosphonic acid compound with an alkylene di- or polyamine followed by guanidation of the so obtained product. The compounds are particularly useful as fungicides and especially as fungicides for industrial purposes. |
| priorityDate | 1983-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 100.