RU96115180A - 1,3-OXAZIN-4-ONE DERIVATIVE, HERBICIDE, CONTAINING THIS DERIVATIVE AND INTERMEDIATE CONNECTION TO OBTAIN THE INDICATED DERIVATIVE - Google Patents
1,3-OXAZIN-4-ONE DERIVATIVE, HERBICIDE, CONTAINING THIS DERIVATIVE AND INTERMEDIATE CONNECTION TO OBTAIN THE INDICATED DERIVATIVEInfo
- Publication number
- RU96115180A RU96115180A RU96115180/04A RU96115180A RU96115180A RU 96115180 A RU96115180 A RU 96115180A RU 96115180/04 A RU96115180/04 A RU 96115180/04A RU 96115180 A RU96115180 A RU 96115180A RU 96115180 A RU96115180 A RU 96115180A
- Authority
- RU
- Russia
- Prior art keywords
- group
- derivative
- active ingredient
- lower alkyl
- hydrogen atom
- Prior art date
Links
- 230000002363 herbicidal Effects 0.000 title claims 10
- TZBHPYXJOJGKDT-UHFFFAOYSA-N 1,3-oxazin-4-one Chemical class O=C1C=COC=N1 TZBHPYXJOJGKDT-UHFFFAOYSA-N 0.000 title claims 5
- 239000004009 herbicide Substances 0.000 title claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 11
- 239000004480 active ingredient Substances 0.000 claims 10
- 239000000203 mixture Substances 0.000 claims 10
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 9
- 150000001875 compounds Chemical class 0.000 claims 8
- -1 N-Methylene amino Chemical group 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 125000004438 haloalkoxy group Chemical group 0.000 claims 4
- 125000001188 haloalkyl group Chemical group 0.000 claims 4
- 125000005843 halogen group Chemical group 0.000 claims 4
- 241000196324 Embryophyta Species 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- XZIDTOHMJBOSOX-UHFFFAOYSA-N 2,3,6-TBA Chemical compound OC(=O)C1=C(Cl)C=CC(Cl)=C1Cl XZIDTOHMJBOSOX-UHFFFAOYSA-N 0.000 claims 1
- 239000005631 2,4-D Substances 0.000 claims 1
- 239000002794 2,4-DB Substances 0.000 claims 1
- YOYAIZYFCNQIRF-UHFFFAOYSA-N 2,6-Dichlorobenzonitrile Chemical compound ClC1=CC=CC(Cl)=C1C#N YOYAIZYFCNQIRF-UHFFFAOYSA-N 0.000 claims 1
- YUVKUEAFAVKILW-UHFFFAOYSA-N 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 YUVKUEAFAVKILW-UHFFFAOYSA-N 0.000 claims 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 1
- NDUPDOJHUQKPAG-UHFFFAOYSA-N Dalapon Chemical compound CC(Cl)(Cl)C(O)=O NDUPDOJHUQKPAG-UHFFFAOYSA-N 0.000 claims 1
- 239000005504 Dicamba Substances 0.000 claims 1
- IWEDIXLBFLAXBO-UHFFFAOYSA-N Dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims 1
- MZHCENGPTKEIGP-UHFFFAOYSA-N Dichlorprop Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 claims 1
- 239000005506 Diclofop Substances 0.000 claims 1
- OOLBCHYXZDXLDS-UHFFFAOYSA-N Diclofop Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(Cl)C=C1Cl OOLBCHYXZDXLDS-UHFFFAOYSA-N 0.000 claims 1
- OFDYMSKSGFSLLM-UHFFFAOYSA-N Dinitramine Chemical compound CCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C(N)=C1[N+]([O-])=O OFDYMSKSGFSLLM-UHFFFAOYSA-N 0.000 claims 1
- OWZPCEFYPSAJFR-UHFFFAOYSA-N Dinoseb Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O OWZPCEFYPSAJFR-UHFFFAOYSA-N 0.000 claims 1
- QAHFOPIILNICLA-UHFFFAOYSA-N Diphenamid Chemical compound C=1C=CC=CC=1C(C(=O)N(C)C)C1=CC=CC=C1 QAHFOPIILNICLA-UHFFFAOYSA-N 0.000 claims 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N Diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims 1
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N Dirurol Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 claims 1
- 239000005510 Diuron Substances 0.000 claims 1
- 239000005572 Lenacil Substances 0.000 claims 1
- 239000005573 Linuron Substances 0.000 claims 1
- UMKANAFDOQQUKE-UHFFFAOYSA-N Nitralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(C)(=O)=O)C=C1[N+]([O-])=O UMKANAFDOQQUKE-UHFFFAOYSA-N 0.000 claims 1
- XITQUSLLOSKDTB-UHFFFAOYSA-N Nitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(Cl)C=C1Cl XITQUSLLOSKDTB-UHFFFAOYSA-N 0.000 claims 1
- 240000007594 Oryza sativa Species 0.000 claims 1
- 235000007164 Oryza sativa Nutrition 0.000 claims 1
- 239000005591 Pendimethalin Substances 0.000 claims 1
- CHIFOSRWCNZCFN-UHFFFAOYSA-N Pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 claims 1
- 239000005595 Picloram Substances 0.000 claims 1
- NQQVFXUMIDALNH-UHFFFAOYSA-N Picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 claims 1
- UNLYSVIDNRIVFJ-UHFFFAOYSA-N Piperophos Chemical compound CCCOP(=S)(OCCC)SCC(=O)N1CCCCC1C UNLYSVIDNRIVFJ-UHFFFAOYSA-N 0.000 claims 1
- YLPGTOIOYRQOHV-UHFFFAOYSA-N Pretilachlor Chemical compound CCCOCCN(C(=O)CCl)C1=C(CC)C=CC=C1CC YLPGTOIOYRQOHV-UHFFFAOYSA-N 0.000 claims 1
- MFOUDYKPLGXPGO-UHFFFAOYSA-N Propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 claims 1
- LFULEKSKNZEWOE-UHFFFAOYSA-N Propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 claims 1
- FKERUJTUOYLBKB-UHFFFAOYSA-N Pyrazoxyfen Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=CC=C1 FKERUJTUOYLBKB-UHFFFAOYSA-N 0.000 claims 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N Simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 claims 1
- NBQCNZYJJMBDKY-UHFFFAOYSA-N Terbacil Chemical compound CC=1NC(=O)N(C(C)(C)C)C(=O)C=1Cl NBQCNZYJJMBDKY-UHFFFAOYSA-N 0.000 claims 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N Trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 239000012141 concentrate Substances 0.000 claims 1
- 150000004891 diazines Chemical class 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000000839 emulsion Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 239000008187 granular material Substances 0.000 claims 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 claims 1
- ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 claims 1
- XKJMBINCVNINCA-UHFFFAOYSA-N linuron Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 claims 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 claims 1
- 150000002903 organophosphorus compounds Chemical class 0.000 claims 1
- 125000004430 oxygen atoms Chemical group O* 0.000 claims 1
- AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 claims 1
- ASRAWSBMDXVNLX-UHFFFAOYSA-N pyrazolate Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OS(=O)(=O)C1=CC=C(C)C=C1 ASRAWSBMDXVNLX-UHFFFAOYSA-N 0.000 claims 1
- 235000009566 rice Nutrition 0.000 claims 1
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 claims 1
- 239000004546 suspension concentrate Substances 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 150000003672 ureas Chemical class 0.000 claims 1
- 239000004563 wettable powder Substances 0.000 claims 1
Claims (23)
где R1 представляет собой фенильную группу, которая может быть замещенной;
R2 представляет собой атом водорода или низшую алкильную группу;
R3 представляет собой атом водорода, низшую алкильную группу, аралкильную группу или фенильную группу, которая может быть замещенной;
R4 и R5 независимо представляет собой низшую алкильную группу, а
W представляет собой атом кислорода или группу, имеющую формулу -N(R6)-, в которой R6 представляет собой атом водорода, низшую алкильную группу, низшую алкенильную группу или низшую алкинильную группу.1. Derived 1,3-oxazin-4-one, having the General formula I:
where R 1 represents a phenyl group which may be substituted;
R 2 represents a hydrogen atom or a lower alkyl group;
R 3 represents a hydrogen atom, a lower alkyl group, an aralkyl group or a phenyl group which may be substituted;
R 4 and R 5 independently represents a lower alkyl group, and
W represents an oxygen atom or a group having the formula —N (R 6 ) -, in which R 6 represents a hydrogen atom, a lower alkyl group, a lower alkenyl group or a lower alkynyl group.
где X1, X2 и X3 независимо представляет собой атом водорода, атом галогена, низшую алкильную группу, низшую алкокси-группу, фенокси-группу, низшую галогеноалкильную группу или низшую галогеноалкокси-группу.8. The 1,3-oxazin-4-one derivative according to claim 1, having the general formula II:
where X 1 , X 2 and X 3 independently represents a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a phenoxy group, a lower haloalkyl group or a lower halogenoalkoxy group.
X2 представляет собой атом водорода; и
X3 представляет собой атом галогена, низшую алкильную группу, низшую алкокси-группу, фенокси-группу, низшую галогеноалкильную группу или низшую галогеноалкокси-группу.9. The compound according to claim 8, wherein X 1 is a fluorine atom;
X 2 represents a hydrogen atom; and
X 3 represents a halogen atom, a lower alkyl group, a lower alkoxy group, a phenoxy group, a lower haloalkyl group or a lower halo alkoxy group.
где R4 и R5 независимо представляют собой низшую алкильную группу, а R10 представляет собой низшую алкильную группу или аралкильную группу.11. N-Methylene amino acid ester derivative of general formula (II):
where R 4 and R 5 independently represent a lower alkyl group, and R 10 represents a lower alkyl group or aralkyl group.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32673393 | 1993-12-24 | ||
JP5-326733 | 1993-12-24 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU96115180A true RU96115180A (en) | 1998-10-20 |
RU2125562C1 RU2125562C1 (en) | 1999-01-27 |
Family
ID=18191077
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU96115180A RU2125562C1 (en) | 1993-12-24 | 1994-12-20 | Derivatives of 1,3-oxazine-4-one, derivative of n-methylene- -amino acid ester, herbicide composition, method of struggle against weed |
Country Status (23)
Country | Link |
---|---|
US (1) | US5977025A (en) |
EP (1) | EP0736019B1 (en) |
JP (1) | JP3763416B2 (en) |
KR (1) | KR100362548B1 (en) |
CN (1) | CN1063441C (en) |
AU (1) | AU680579B2 (en) |
BG (1) | BG100717A (en) |
BR (1) | BR9408419A (en) |
CO (1) | CO4520266A1 (en) |
CZ (1) | CZ182896A3 (en) |
DE (1) | DE69432756T2 (en) |
ES (1) | ES2196051T3 (en) |
FI (1) | FI962587A (en) |
HU (1) | HU224864B1 (en) |
IL (1) | IL112014A (en) |
MA (1) | MA23418A1 (en) |
PL (1) | PL315180A1 (en) |
RU (1) | RU2125562C1 (en) |
SK (1) | SK82796A3 (en) |
TR (1) | TR28348A (en) |
UA (1) | UA48942C2 (en) |
WO (1) | WO1995018113A1 (en) |
ZA (1) | ZA9410268B (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08151364A (en) * | 1994-02-18 | 1996-06-11 | Nissan Chem Ind Ltd | Nitrogen-containing cyclic compound and herbicide |
GB9512819D0 (en) * | 1995-06-23 | 1995-08-23 | Rhone Poulenc Agriculture | Herbicides |
IL124767A0 (en) * | 1995-12-11 | 1999-01-26 | Rhone Poulenc Agriculture | 1, 3-Oxazin-4-one derivatives as herbicides |
GB9608399D0 (en) * | 1996-04-23 | 1996-06-26 | Mitsubishi Chemical Company | New Herbicides |
PT102162B (en) * | 1997-06-10 | 2001-05-31 | Rhone Poulenc Agriculture | HERBICIDES |
GB9818666D0 (en) * | 1998-08-27 | 1998-10-21 | Rhone Poulenc Agriculture | New herbicidal method |
GB2343179A (en) * | 1998-10-26 | 2000-05-03 | Rhone Poulenc Agrochimie | Oxazinone and pyridone herbicides |
RU2643143C2 (en) * | 2012-06-19 | 2018-01-31 | Дау Глоубл Текнолоджиз Ллк | Antimicrobial substances |
EA026242B1 (en) * | 2012-07-02 | 2017-03-31 | Ред Суркос С.А. | Phytosanitary compositions and spraying products in the form of microemulsions |
CN105764898A (en) | 2013-09-11 | 2016-07-13 | 先正达参股股份有限公司 | Heterocyclic amide compound and herbicide |
CN103766354B (en) * | 2013-12-09 | 2017-01-04 | 广东中迅农科股份有限公司 | A kind of containing metribuzin with the Herbicidal combinations of bentazone |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3718688A (en) * | 1967-10-18 | 1973-02-27 | Radio Carbon Lab | Alkylidine and arylidine amino acid esters, and alkyl and aryl amino acid esters |
NZ178996A (en) * | 1974-11-15 | 1978-06-02 | Kornis G | Pyrfazole amides and thioamides;herbicidal compositions |
WO1982000402A1 (en) * | 1980-08-07 | 1982-02-18 | Shamrock Corp Diamond | Herbicidal and plant growth regulant diphenylpyridazinones |
EG18833A (en) * | 1988-12-09 | 1994-11-30 | Kumiai Chemical Industry Co | Cyclic amide compounds and herbicides |
JPH082884B2 (en) * | 1990-07-30 | 1996-01-17 | ダイセル化学工業株式会社 | 1,3-Oxazin-4-one derivative, its production method and plant growth inhibitor |
AU652310B2 (en) * | 1992-01-30 | 1994-08-18 | Bayer Cropscience K.K. | 1,3-oxazin-4-one derivative, herbicide containing the same, and novel intermediate for producing the same |
JPH05221972A (en) * | 1992-02-17 | 1993-08-31 | Kumiai Chem Ind Co Ltd | 2-@(3754/24)2-oxo-3-pyrrolin-1-yl)isobutyric acid derivative and herbicide |
US5312929A (en) * | 1992-02-17 | 1994-05-17 | Kumiai Chemical Industry Co., Ltd. | 2-oxo-3-pyrroline derivatives, process for their production and herbicidal composition |
JPH07112976A (en) * | 1993-10-14 | 1995-05-02 | Mitsubishi Chem Corp | 1,3-oxazin-4-one derivative and herbicide using the same as active ingredient and intermediate for the same |
-
1994
- 1994-12-16 IL IL11201494A patent/IL112014A/en not_active IP Right Cessation
- 1994-12-20 BR BR9408419A patent/BR9408419A/en not_active IP Right Cessation
- 1994-12-20 SK SK827-96A patent/SK82796A3/en unknown
- 1994-12-20 RU RU96115180A patent/RU2125562C1/en not_active IP Right Cessation
- 1994-12-20 CN CN94194637A patent/CN1063441C/en not_active Expired - Lifetime
- 1994-12-20 UA UA96062476A patent/UA48942C2/en unknown
- 1994-12-20 DE DE69432756T patent/DE69432756T2/en not_active Expired - Fee Related
- 1994-12-20 KR KR1019960703396A patent/KR100362548B1/en not_active IP Right Cessation
- 1994-12-20 JP JP51788895A patent/JP3763416B2/en not_active Expired - Lifetime
- 1994-12-20 WO PCT/JP1994/002152 patent/WO1995018113A1/en active IP Right Grant
- 1994-12-20 CZ CZ961828A patent/CZ182896A3/en unknown
- 1994-12-20 ES ES95903002T patent/ES2196051T3/en not_active Expired - Lifetime
- 1994-12-20 PL PL94315180A patent/PL315180A1/en unknown
- 1994-12-20 AU AU12018/95A patent/AU680579B2/en not_active Ceased
- 1994-12-20 EP EP95903002A patent/EP0736019B1/en not_active Expired - Lifetime
- 1994-12-20 HU HU9601723A patent/HU224864B1/en not_active IP Right Cessation
- 1994-12-20 US US08/663,118 patent/US5977025A/en not_active Expired - Fee Related
- 1994-12-21 MA MA23734A patent/MA23418A1/en unknown
- 1994-12-22 TR TR01335/94A patent/TR28348A/en unknown
- 1994-12-22 ZA ZA9410268A patent/ZA9410268B/en unknown
- 1994-12-23 CO CO94058033A patent/CO4520266A1/en unknown
-
1996
- 1996-06-20 FI FI962587A patent/FI962587A/en not_active Application Discontinuation
- 1996-07-17 BG BG100717A patent/BG100717A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS59118701A (en) | Herbicides | |
JPH06501674A (en) | Methods and compositions for promoting absorption and translocation of bioactive agents in plants | |
HU229840B1 (en) | Sulfamoyl compounds and agricultural and horticultural fungicide compositions | |
EP0563384A4 (en) | Uracil derivative | |
RU96115180A (en) | 1,3-OXAZIN-4-ONE DERIVATIVE, HERBICIDE, CONTAINING THIS DERIVATIVE AND INTERMEDIATE CONNECTION TO OBTAIN THE INDICATED DERIVATIVE | |
KR880011184A (en) | Phenoxycarboxylic acid and herbicide containing it as an active ingredient | |
US5672566A (en) | Synergistic herbicidal compositions comprising 1,3-oxazin-4-one compounds | |
CA2182773C (en) | A composition for regulating plant growth and a method for application thereof | |
GR3018155T3 (en) | Compositions having herbicidal activity containing N-Alkyl-amides as active ingredient. | |
RU2117429C1 (en) | Herbicide composition | |
HUT77881A (en) | 3-benzoylpyridine derivatives, herbicide compositions containing these compounds as active ingredients and use thereof | |
HU176584B (en) | Herbicide preparation containing of active mateirals of two types | |
JP2005504106A (en) | Herbicidal composition containing pyriftalide | |
US4032325A (en) | Method for controlling weeds with amino acid higher alkyl esters | |
US4806653A (en) | Process for preparation of iminooxazolidines | |
SU1452457A3 (en) | Method of controlling undesirable vegetation | |
KR960704867A (en) | Novel 1,3-oxazin-4-one derivatives, herbicides containing them and intermediates for their preparation (NOVEL 1,3-OXAZIN-4-ONE DERIVATIVES, HERBICIDES CONTAINING THE SAME, AND INTERMEDIATES FOR PREPARING THE SAME) | |
US4174210A (en) | Herbicidal and plant-growth regulating N-haloacetylphenylamino carbonyl oximes | |
EP0146238A1 (en) | Synergistic herbicidal composition | |
RU2048772C1 (en) | Herbicide composition | |
WO1997035481A1 (en) | Herbicidal composition | |
US4416684A (en) | Synergistic herbicidal compositions | |
JP2005533127A (en) | Novel benzohydrazide derivatives as herbicides and desiccant compositions containing them | |
KR970707119A (en) | TRIAZOLE DERIVATIVES, HERBICIDE COMPOSITION CONTAINING THE SAME, AND METHOD FOR USING THE SAME. | |
JP3474611B2 (en) | Herbicide composition |