http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2703460-C1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_315ae544538aaeac6d1f4eed6754e4bb |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-82 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-647 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D403-12 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-647 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D403-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01P13-00 |
| filingDate | 2014-12-09^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2019-10-17^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2f953e026e5a4b0dd845dd9f2273812d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9c9318f3324a0f8be2983307037b638b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_19d82219901cc76ee3a1400e56cc10cf http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f103e3e0bbc79cea7bde95c8401117e8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dcca8e5fe7d9a773ac0e07da69ef1ef0 |
| publicationDate | 2019-10-17^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | RU-2703460-C1 |
| titleOfInvention | Herbicidal substituted pyrimidinyloxybenzole compounds |
| abstract | FIELD: chemistry. n SUBSTANCE: invention relates to a novel compound of formula 1 or a salt thereof. In the compound of formula 1 n n n n 1 -Y 1 = Y 2 -Y 3 = Y 4 -, including nitrogen atom, to which are connected as Y 1 , and Y 4 , selected from n n n n Z is O or S; each R 1 independently represents hydrogen, halogen, cyano, nitro, CHO, C(= O)NH 2 , SO 2 NH 2 , C 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 1 -C 4 haloalkyl, C 3 -C 6 cycloalkyl, C 2 -C 6 alkylcarbonyl, C 2 -C 6 alkoxycarbonyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy, C 2 -C 6 cyanoalkoxy, SO n R 1A , Si (CH 3 ) 3 , C (= (NOH) CH 3 or B (-OC (R 1B ) 2 C (R 1B ) 2 O-); or a phenyl ring optionally substituted with not more than 5 substitutes independently selected from R 1C ; or 5- or 6-member heteroaromatic ring containing ring members selected from carbon atoms and not more than 4 heteroatoms independently selected from at most 2 O atoms, not more than 2 S atoms and not more than 4 N atoms, wherein each ring is optionally substituted with not more than 3 substitutes independently selected from R 1C by ring members, which are carbon atoms, and R 1D by ring members, which are nitrogen atoms; R 2 is halogen, cyano, nitro, C 1 -C 4 alkoxy, C 1 -C 4 alkyl, C 2 -C 6 alkynyl or C 1 -C 4 haloalkyl; m is 0, 1, 2 or 3; each R 3 independently represents halogen, cyano, hydroxy, nitro, CHO, C(= O)NH 2 , C(= S)NH 2 , C 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 2 -C 4 alkynyl, C 1 -C 4 haloalkyl, C 2 -C 6 alkylcarbonyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy, C 2 -C 4 alkylcarbonyloxy, C≡CSi (CH 3 ) 3 , C (= O) N (R 3A ) (R 3B ), C (= NOR 3C ) H, C (= NR 3D ) H, SO n R 3E ; or a phenyl ring optionally substituted with not more than 5 substitutes independently selected from R 3F ; or 5- or 6-member heteroaromatic ring containing ring members selected from carbon atoms and not more than 4 heteroatoms independently selected from at most 2 O atoms, not more than 2 S atoms and not more than 4 N atoms, wherein each ring is optionally substituted with not more than 3 substitutes independently selected from R 3F by ring members, which are carbon atoms, and R 3G by ring members, which are nitrogen atoms; or pyrimidinyloxy; each n is independently equal to 0, 1 or 2; each R 1A independently represents C 1 -C 4 haloalkyl, C 1 -C 4 alkylamino or C 2 -C 6 dialkylamino; each R 1B independently represents H or C 1 -C 4 alkyl; each R 1C independently represents halogen, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy or C 1 -C 6 haloalkoxy; each R 1D independently is cyano, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy or C 2 -C 6 alkylcarbonyl; each R 3A independently represents C 1 -C 4 alkyl; each R 3B independently represents H or C 1 -C 4 alkyl; each R 3C independently represents H or C 1 -C 4 alkyl; each R 3D independently represents H, amino, C 1 -C 4 alkyl or C 1 -C 4 alkylamino; each R 3E independently represents C 1 -C 4 alkyl, C 1 -C 4 alkylamino or C 2 -C 6 dialkylamino; each R 3F independently represents hydroxy, halogen, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy or C 1 -C 6 haloalkoxy; and each R 3G independently represents C 1 -C 6 alkyl, C 1 -C 6 haloalkyl or C 1 -C 6 6alkoxy. Invention also relates to a herbicidal composition containing herbicidally effective amount of compound of 1 and at least one component selected from a group consisting of surfactants, solid diluents and liquid diluents. n EFFECT: compounds have herbicidal properties and can be used to control growth of undesirable vegetation, including contact of vegetation or its environment in herbicidally effective amount. n 9 cl, 6 tbl, 12 ex |
| priorityDate | 2013-12-10^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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