http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-486649-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-76 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-86 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-52 |
| filingDate | 1979-12-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1980-06-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-486649-A1 |
| titleOfInvention | PROCEDURE FOR OBTAINING SUSPIUTE SPIRAL DERIVATIVES OF 3- (3,5-DIHALOGENOFENIL) -OXAZOLIDIN-2,4-DIONAS (TION-ONAS) OF FUNGICIDE EFFECT |
| abstract | New spiro substituted derivatives of 3- (3,5-dihalogenophenyl) -oxazolidin-2,4-diones (thion-ones), to various procedures for their production as well as to their use as fungicides. Thiuramic disulfides, such as for example tetramethylthiuramic disulfide show good fungicidal properties. The effect of both classes of substances is not always fully satisfactory in certain indication areas, especially with low application amounts and concentrations. The spiro-substituted derivatives of 3- (3,5-dihalogen-phenyl) -axazolidin-2,4-diones (thion-ones) of formula ** (Formula) ** where A have now been discovered as new compounds means oxygen or sulfur, X and Y are the same or different and mean halogen, Z means fused alkyl or cycloalkyl, or cycloalkenyl, m represents the integers 1, 2, 3 or 4 and n represents the integers 2 or 3. |
| priorityDate | 1978-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 19.