http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1093247-A3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_13b33da90a97d6236edf4f75c3c79e8d |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N41-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D275-06 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N41-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C301-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D275-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D275-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-16 |
| filingDate | 1981-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1984-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7fd933da5e080b6df8cebb2f9ed76eda http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c272779eb7df3cb5d652998d6d3b1ed http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b0e5cd9bee46392664948cc8b271e0c5 |
| publicationDate | 1984-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | SU-1093247-A3 |
| titleOfInvention | Process for preparing substituted isothiazole-1,1-dioxides |
| abstract | The invention relates to new sulphonyl compounds of the general formulan whereinn X is a halogen atom, a phenoxy group, or an alkyl group or alkoxy group having 1-4 carbon atoms and substituted, if desired, with halogen; R 1 is a cyano group, and R 2 is an amino group which, if desired, may be substituted with halogen, with one or two alkenyl groups or alkynyl groups having 2-6 carbon atoms or with one or two alkyl groups having 1-6 carbon atoms, which alkyl groups. together with the nitrogen atom to which they are bound may form a saturated heterocyclic ring which ring may also contain a second hetero atom seieted from the group consisting of nitrogen oxygen and suiphor or which alkyl groups may be substituted with an alkoxy group having 1-4 carbon atoms, or with a olalkylamine group having 2-6 carbon atoms the alkyl groups of which, together with the nitrogen atom to which they are bound, may form a saturated heterocyclic ring; or wherein Ri and R 2 together form a S,S-dialkylsulphox- imido group the alkyl groups of which comprise 1-4 carbon atoms, or a 1-amino-2-azavinylene group, of which the amino group is substituted, if desired, with a cycloalkylcarbamoyl group having 4-8 carbon atoms, an alkylcarbamoyl group having 2-5 carbon atoms, a dialkylamino group the alkyl group of which comprise 1-4 carbon atoms, or an alkyl group having 1-4 carbon atoms which alkyl group may be substituted with a hydroxy group or one or more halogen atoms; or wherein R 1 and R 2 together form a 1-imino-2-azaethy- lene group of which the ring nitrogen is substituted with an alkyl group or alkenyl group having 1-4 carbon atoms, and of wich the imino group may be substituted with a substituted or non-substituted phenyl-carbamoyl group, having aphicidal activity After having been processed to compositions the compounds may be used for the control of aphids in agriculture and forestry in a dosage from 20 to 5,000 g of actve substance per hectare |
| priorityDate | 1980-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
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