http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2106844-A1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-16 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D521-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-60 |
| filingDate | 1971-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1972-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | DE-2106844-A1 |
| titleOfInvention | 2-heteroaryl-naphthohydroquinone derivs - with fungicidal and herbicidal activity |
| abstract | Title cpds. of formula (I): (where X is H, alkyl, halogen, NO2 or aminosulphonyl; Y is H, -N or -CH2-N; -N is a 5-membered hetero-aromatic residue contg. a total of 2 or 3 N-atoms in the ring and opt. substd. by up to 2 alkyl or halogen residues; and n is 1 or 2), which are also inters for plant-protection agents and pesticides, are prepd. by reacting a 1,4-naphthoquinone derivative of formula (II): (where Z is H, CH3) or alkoxy) with H-N at 50 - 180 degrees C (pref. 50 - 150 degrees C), if necessary in the presence of diluents and under elevated pressure. |
| priorityDate | 1971-02-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 45.