http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-088616-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_96ec3985e3ce9b24614fb87bf51a4f12 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D257-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-713 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-653 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D257-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-653 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-713 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-32 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-653 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D257-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-713 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 |
| filingDate | 2012-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3cd0a3ee965645f5b5345b8978383f77 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_26d1cd65dbc42223bc5a188691d732ae http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cc4ba387a517d5bb52b33e46e0f05bea http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31e2b588b87520445332decf057288fe http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6462676b14d2a0f67ddadcd17cc41ba2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1de1de734ad48c5834be88b585eef168 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_af620b7d0287ae6da79bd62c2bb25737 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_90e72f790c573b6ab33b1788986860d0 |
| publicationDate | 2014-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-088616-A1 |
| titleOfInvention | HERBICIDE-SELECTIVE PROTECTOR COMBINATIONS CONTAINING AMIDES OF N- (TETRAZOL-5-IL) -CARBONIC AND N- (TRIAZOL-5-IL) ARILCARBONIC ACIDS |
| abstract | Claim 1: Selective herbicide-protective combinations containing (A) one or more compounds of the formula (1) or their salts, wherein the symbols and indices have the following meanings: A means N or CY; B means N or CH; X means nitro, halogen, cyano, formyl, rhodan, C₁₋₆ alkyl, halogen-C₁₋₆ alkyl, C₂₋₆ alkenyl, halogen-C₂₋₆ alkenyl, C₂₋₆ alkynyl, halogen-C₃₋₆ alkynyl, C₃ cycloalkyl ₋₆, halogen-C₃₋₆-cycloalkyl, C₃₋₆-cycloalkyl-C₁₋₆-alkyl, halogen-C₃₋₆ -cycloalkyl-C alquilo-alkyl, COR¹, COOR¹, OCOOR¹, NR¹COOR¹, C (O) N (R¹) ₂, NR¹C (O) N (R¹) ₂, OC (O) N (R¹) ₂, C (O) NR¹OR¹, OR¹, OCOR¹, OSO²R², S (O) ₙR², SO₂OR¹, SO₂N (R¹) ₂, NR¹SO₂R², NR¹COR¹, C₁₋₆-S (O) ₙR² alkyl, C₁₋₆-OR¹ alkyl, C₁₋₆-OCOR¹ alkyl, C₁₋₆-OSO₂R² alkyl, C₁₋₆-CO₂R¹ alkyl, C₁₋₆-SO₂OR¹ alkyl, C₁₋₆ alkyl -CON (R¹) ₂, C₁₋₆-SO₂N (R¹) ₂ alkyl, C₁₋₆-NR¹COR¹ alkyl, C₁₋₆-NR¹SO₂R² alkyl, NR¹R², P (O) (OR⁵) ₂, CH₂P (O) (OR⁵) ₂, C₁₋₆-heteroaryl alkyl, C₁₋₆-heterocyclyl alkyl, the last two moieties being substituted s mentioned respectively with s residues of the group consisting of halogen, C₁₋₆ alkyl, halogen-C₁₋₆ alkyl, S (O) ₙ -C alquilo alkyl, C₁₋₆ alkoxy and halogen-C₁₋₆ alkoxy, and carrying the heterocyclyl n oxo groups; Y means hydrogen, nitro, halogen, cyano, rhodan, C₁₋₆ alkyl, halogen-C₁₋₆ alkyl, Cque alkenyl, C₂₋₆ halogen-alkenyl, C₂₋₆ alkynyl, C₂₋₆ halogen-alkynyl, C₃ cycloalkyl ₋₆, C₃₋₆ cycloalkenyl, C₃₋₆ halogen-cycloalkyl, C₃₋₆ cycloalkyl-C₁₋₆ alkyl, halogen-C₃₋₆ -cycloalkyl-C alquilo alkyl, COR¹, COOR¹, OCOOR¹, NR¹COOR¹, C (O) N (R¹) ₂, NR¹C (O) N (R¹) ₂, OC (O) N (R¹) ₂, CO (NOR¹) R¹, NR¹SO₂R², NR¹COR¹, OR¹, OSO₂R², S (O) ₙR², SO₂OR¹, SO₂N (R¹ ) ₂, C₁₋₆-S (O) alkyl ₙR², C₁₋₆-OR¹ alkyl, C₁₋₆-OCOR¹ alkyl, C₁₋₆-OSO₂R² alkyl, C₁₋₆-CO₂R¹ alkyl, C₁₋₆-CN alkyl, alkyl C₁₋₆-SO₂OR¹, C₁₋₆-CON (R¹) ₂ alkyl, C₁₋₆-SO₂N (R¹) ₂ alkyl, C₁₋₆-NR¹COR¹ alkyl, C₁₋₆-NR¹SO₂R² alkyl, N (R¹) ₂, P ( O) (OR⁵) ₂, CH₂P (O) (OR⁵) ₂, C₁₋₆-phenyl alkyl, C₁₋₆-heteroaryl alkyl, al C₁₋₆-heterocyclyl, phenyl, heteroaryl or heterocyclyl, the last six moieties mentioned respectively being substituted with s moieties of the group consisting of halogen, nitro, cyano, C₁₋₆ alkyl, halogen-C₁₋₆ alkyl, C₃₋₆ cycloalkyl , S (O) ₙ-C₁₋₆ alkyl, C₁₋₆ alkoxy, halogen-C₁₋₆ alkoxy, C₁₋₆ alkoxy-C₁₋₄ alkyl and cyanomethyl, and carrying the heterocyclyl n oxo groups; Z means halogen, cyano, rhodan, halogen-C₁₋₆ alkyl, C₂₋₆ alkenyl, halogen-C₂₋₆ alkenyl, C₂₋₆ alkynyl, halogen-C₂₋₆ alkynyl, C₃₋₆ cycloalkyl, C₃₋₆ halogen-cycloalkyl , C₃₋₆ cycloalkyl-C₁₋₆ alkyl, halogen-C₃₋₆ cycloalkyl-C alquilo alkyl, COR¹, COOR¹, OCOOR¹, NR¹COOR¹, C (O) N (R¹) ₂, NR¹C (O) N (R¹) ₂ , OC (O) N (R¹) ₂, C (O) NR¹OR¹, OSO₂R², S (O) ₙR², SO₂OR¹, SO₂N (R¹) ₂, NR¹SO₂R², NR¹COR¹, C₁₋₆-S (O) ₙR² alkyl, C₁ alkyl ₋₆-OR¹, C₁₋₆-OCOR¹ alkyl, C₁₋₆-OSO₂R² alkyl, C₁₋₆-CO₂R¹ alkyl, C₁₋₆-SO₂OR¹ alkyl, C₁₋₆-CON (R¹) alkyl ₂, C₁₋₆-SO₂N alkyl (R¹) ₂, C₁₋₆-NR¹COR¹ alkyl, C₁₋₆-NR¹SO₂R² alkyl, N (R¹) ₂, P (O) (OR⁵) ₂, heteroaryl, heterocyclyl or phenyl, the last three moieties mentioned respectively being substituted with s remains of the group consisting of halogen, nitro, cyano, alky C₁₋₆-yl, halogen-C₁₋₆ alkyl, C₃₋₆ cycloalkyl, S (O) ₙ -Cₙ alkyl, C₁₋₆ alkoxy or halogen-C₁₋₆ alkoxy, and carrying the heterocyclyl n oxo groups, or Z it can also mean hydrogen, C₁₋₆ alkyl or C₁₋₆ alkoxy, if Y represents the remainder S (O) ₙR²; W means hydrogen, C₁₋₆ alkyl, halogen-C₁₋₆ alkyl, C₂₋₆ alkenyl, C₂₋₆ halogen-alkenyl, C₂₋₆ alkynyl, C₂₋₆ halogen-alkynyl, C₃₋₇ cycloalkyl, C-halocycloalkyl , C₁₋₆ alkoxy, C₁₋₆ haloalkoxy, S (O) ₙ-C₁₋₆ alkyl, S (O) ₙ -C halo haloalkyl, C₁₋₆ alkoxy-C₁₋₄ alkyl, C₁₋₆ alkoxy-C₁ haloalkyl ₋₄, halogen, nitro, NR³COR³ or cyano; R means C₁₋₈ alkyl, halogen-C₁₋₈ alkyl, C₂₋₈ alkenyl, C₂₋₈ halogen-alkenyl, C₂₋₈ alkynyl, halogen-C₂₋₈ alkynyl, these six moieties mentioned respectively being substituted with s moieties of the group formed by hydroxy, nitro, cyano, SiR⁵₃, PO (OR⁵) ₂, S (O) ₙ-C₁₋₆ alkyl, S (O) ₙ -C₁₋₆ haloalkyl, C₁₋₆ alkoxy, halogen-C₁₋₆ alkoxy, N (R³) ₂, COR³, COOR³, OCOR³, NR³COR³, NR³SO₂R⁴, O-C₁₋₂-C-cycloalkyl alkyl, C₃₋₆ cycloalkyl, heteroaryl, heterocyclyl, phenyl, Q-heteroaryl, Q-heterocyclyl, Q-phenyl and Q-benzyl, the last seven moieties mentioned respectively being substituted with s moieties of the group consisting of methyl, ethyl, methoxy, trifluoromethyl, cyano and halogen, and carrying the heterocyclyl n oxo groups, or R respectively means C₃₋₇ cycloalkyl, heteroaryl , heterocyclyl or phenyl substituted by moieties of the group formed by halogen eno, nitro, cyano, C₁₋₆ alkyl, halogen-C₁₋₆ alkyl, C₃₋₆ cycloalkyl, S (O) ₙ -C alquilo alkyl, C₁₋₆ alkoxy, C₁₋₆ halogen-alkoxy and C₁₋₆ alkoxy -C₁₋₄ alkyl, carrying the heterocyclyl n oxo groups; Q means O, S, or NR³; R¹ means hydrogen, C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₂₋₆ alkenyl, C₂₋₆ haloalkenyl, C₂₋₆ alkynyl, C₂₋₆ cycloalkyl, C₃₋₆ cycloalkenyl, C₃₋₆ halocycloalkyl, alkyl C₁₋₆-O-C₁₋₆ alkyl, C₃₋₆ cycloalkyl-C₁₋₆ alkyl, phenyl, phenyl-C₁₋₆ alkyl, heteroaryl, C₁₋₆-heteroaryl alkyl, heterocyclyl, C₁₋₆-heterocyclyl alkyl, C₁ alkyl ₋₆-O-heteroaryl, C₁₋₆-O-heterocyclyl alkyl, C₁₋₆-NR³-heteroaryl alkyl or C₁₋₆-NR³-heterocyclyl alkyl, the last 21 moieties mentioned respectively being substituted with s moieties of the cyano group , halogen, nitro, rhodan, OR³, S (O) ₙR⁴, N (R³) ₂, NR³OR³, COR³, OCOR³, SCOR⁴, NR³COR³, NR³SO₂R⁴, CO₂R³, COSR⁴, CON (R³) ₂ and C₁₋₄-alkoxycarbonyl alkoxy ₋₆, and carrying the heterocyclyl n oxo groups; R² means C₁₋₆ alkyl, C₁₋₆ haloalkyl, C₂₋₆ alkenyl, C₂₋₆ haloalkenyl, C₂₋₆ alkynyl, C₃₋₆ haloalkynyl, C₃₋₆ cycloalkenyl, C₃₋₆ halocycloalkyl, C₁₋ alkyl ₆-O-C₁₋₆ alkyl, C₃₋₆ cycloalkyl-C₁ alkyl &# x |
| priorityDate | 2011-11-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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Total number of triples: 43.