http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2338135-T3

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e559abcd8f120b071dc1162360867ffa
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-80
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12
filingDate 2005-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2010-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a8f45734e104903de2db4f5a6199493f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b5db653cafe0c93e181cecfedc6777e4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2f28fb8a2c14a465d3ac0464fba306af
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd472208525402fcaac25791e8e8c076
publicationDate 2010-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2338135-T3
titleOfInvention ISOXAZOLINE DERIVATIVES AND ITS USE AS HERBICIDES.
abstract A compound of the formula I ** (See formula) ** wherein R 1 and R 2 are each independently of the other hydrogen, C 1 -C 10 alkyl, C 1 -C 10 haloalkyl, C 3 -C 8 cycloalkyl or C 3 -C 8 cycloalkyl-C 1 -C 3 alkyl, or R 1 and R2 together with the carbon atom to which they are attached form a C3-C7, R3 and R4 ring are each independently of the other hydrogen, C1-C10 alkyl, C1-C10 haloalkyl, C3-C8-cycloalkyl-C1-C10, C1-C6 alkoxy-C1-alkyl C10 or C3-C8 cycloalkyl, or R3 and R4 together with the carbon atom to which they are attached form a C3-C7 ring, or R1 with R3 or R4 and together with the carbon atoms to which they are attached form a C5-C8 ring, or R2 with R3 or R4 and together with the carbon atoms to which they are attached form a C5-C8, R5 and R6 ring are each independently of the other cyclopropyl, difluoromethyl, trifluoromethyl, trifluoroethyl, hydroxymethyl, methoxymethyl, methylthiomethyl, methylsulfinylmethyl, Methylsulfonylmethyl, vinyl, difluorovinyl, dichlorovinyl, ethynyl, pr opargyl, acetyl, trifluoroacetyl, methoxycarbonylethyl, nitro, formyl, bromine, chlorine, fluorine, iodine, azide, trimethylsilyl, methoxycarbonylmethyl, ethoxycarbonylmethyl, cyanomethyl, cyanoethyl, -CH2CH2CON (CH3) 2, -CH2CH2 (2) -CH2CH2 (2) -CH2CH2 (2) - 2) - CH2CH2P (O) (OC2H5) 2, -CH2CH2COCH3, -CH2CH2COCH2CH3, -CH2CH2CO2CH3, -CH2CH2CO2CH2 H3, -CH2CH2SO2CH3, -CH2CH2NO2, mercapto, phenylthio, methylthio, methylsulfinyl, methylsulfonyl, benzylsulfonyl, phenylsulfinyl, phenylsulfonyl, trifluoromethylthio, trifluoromethylsulfinyl, trifluoromethylsulfonyl, hydroxy , methoxy, ethoxy, trifluoromethoxy, trifluoroethoxy, methanesulfonyloxy, trifluoromethanesulfonyloxy, phenoxy, benzyloxy, -CONH-SO2-CH3, -CONH-SO2-CF3, -NHCO-CH3, -NHCO-CF3, -OCO-CH3, , -OCO-phenyl, -OCONH-CH3, -OCONH-CH2CF3, -OCONH-phenyl, -CONH2, -CONHCH3 or -CON (CH3) 2, and R6 may additionally be hydrogen, cyano, methyl, ethyl, isopropyl, methoxycarbonyl , ethoxycarbonyl or benzyloxycarbonyl, m is 0, 1 or 2, n is 1, 2 or 3, Y is phenyl, naphthyl, tetrahydronaphthi Lo, 1,3-dioxalanyl, tetrahydrofuranyl, morpholinyl, furyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, oxazolyl, isoxazolyl, isothiazolyl, 1,2,3- oxadiazolyl, 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,5-oxadiazolyl, 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,5-thiadiazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, 1,2,3-triazinyl, 1,2,4-triazinyl, 1,3,5-triazinyl, tetrazolyl, tetrazinyl, benzofuryl, benzoisofuryl, benzothienyl, benzoisothienyl, indolyl, benzimidazolyl, 2,1,3-benzoxadiazolyl, quinolyl, isoquinolyl, cinnolinyl, phthalacinyl, quinazolinyl, quinoxalinyl, naphthihydrinyl, benzotriazinyl, purinyl, pteridinyl or indolizinyl, whose rings can be substituted with b, bromine trifluoromethyl, cyclopropyl, methyl, methylthio, methylsulfinyl, methylsulfonyl, trifluoromethylthio, trifluoromethylsulfinyl, trifluoromethylsulfonyl, methoxy, ethoxy, trifluoromethoxy, difluoromethoxy, cyano, nitro, methoxycarbonyl, -CONH2 or with carboxyl, and to the N-oxides, salts and optical isomers of the compounds of the formula I.
priorityDate 2004-09-03-04:00^^<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: 1156.