FI59522C - N-metylkarbanilsyra-(3-(etoxikarbonylamino)-fenyl)-ester anvaendbar som bomullherbicid - Google Patents

N-metylkarbanilsyra-(3-(etoxikarbonylamino)-fenyl)-ester anvaendbar som bomullherbicid Download PDF

Info

Publication number: FI59522C
Authority: FI; Finland
Prior art keywords: ester; phenyl; acid; methylcarbanylsyra; ethoxicarbonylamino
Prior art date: 1976-02-27

Application number

FI770488A

Other languages

English (en)

Finnish (fi)

Other versions

FI770488A7 (cs

FI59522B (fi

Inventor

Friedrich Arndt

Gerhard Boroschewski

Original Assignee

Schering Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1976-02-27

Filing date

1977-02-15

Publication date

1981-09-10

1977-02-15 Application filed by Schering Ag filed Critical Schering Ag

1977-08-28 Publication of FI770488A7 publication Critical patent/FI770488A7/fi

1981-05-29 Publication of FI59522B publication Critical patent/FI59522B/fi

1981-09-10 Application granted granted Critical

1981-09-10 Publication of FI59522C publication Critical patent/FI59522C/fi

Links

241000196324 Embryophyta Species 0.000 description 17
229920000742 Cotton Polymers 0.000 description 9
241000219146 Gossypium Species 0.000 description 9
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
-1 attazavi Substances 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 8
239000000126 substance Substances 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
150000001875 compounds Chemical class 0.000 description 7
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
239000004480 active ingredient Substances 0.000 description 6
230000000694 effects Effects 0.000 description 5
239000004009 herbicide Substances 0.000 description 5
GAUSUDNBBOZKSB-UHFFFAOYSA-N methyl(phenyl)carbamic acid Chemical compound OC(=O)N(C)C1=CC=CC=C1 GAUSUDNBBOZKSB-UHFFFAOYSA-N 0.000 description 5
238000005507 spraying Methods 0.000 description 5
238000003756 stirring Methods 0.000 description 5
240000002024 Gossypium herbaceum Species 0.000 description 4
235000004341 Gossypium herbaceum Nutrition 0.000 description 4
239000000969 carrier Substances 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
KCLZXXMMEDEBMF-UHFFFAOYSA-N ethyl n-(3-hydroxyphenyl)carbamate Chemical compound CCOC(=O)NC1=CC=CC(O)=C1 KCLZXXMMEDEBMF-UHFFFAOYSA-N 0.000 description 4
230000002363 herbicidal effect Effects 0.000 description 4
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 4
238000000034 method Methods 0.000 description 4
239000002689 soil Substances 0.000 description 4
239000007921 spray Substances 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000001816 cooling Methods 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000007788 liquid Substances 0.000 description 3
229910052943 magnesium sulfate Inorganic materials 0.000 description 3
235000019341 magnesium sulphate Nutrition 0.000 description 3
239000000203 mixture Substances 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000013558 reference substance Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
238000003971 tillage Methods 0.000 description 3
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 description 2
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
JDODIRQZJXDLAP-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] carbonochloridate Chemical compound CCOC(=O)NC1=CC=CC(OC(Cl)=O)=C1 JDODIRQZJXDLAP-UHFFFAOYSA-N 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
230000006378 damage Effects 0.000 description 2
DLLJVQNYBYOKGS-UHFFFAOYSA-N ethoxyethane;pentane Chemical compound CCCCC.CCOCC DLLJVQNYBYOKGS-UHFFFAOYSA-N 0.000 description 2
239000005457 ice water Substances 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
238000009331 sowing Methods 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
MXDMRWOMPWYOBI-UHFFFAOYSA-N 1,3-dimethyl-1-[3-(trifluoromethyl)phenyl]urea Chemical compound CNC(=O)N(C)C1=CC=CC(C(F)(F)F)=C1 MXDMRWOMPWYOBI-UHFFFAOYSA-N 0.000 description 1
FXFCLNJIQWLFEL-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-1,3-dimethylurea Chemical compound CNC(=O)N(C)C1=CC=C(Cl)C(Cl)=C1 FXFCLNJIQWLFEL-UHFFFAOYSA-N 0.000 description 1
LGXNQMGCMMSGAI-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-3-methoxy-1-methylurea Chemical compound CONC(=O)N(C)C1=CC=C(Cl)C(Cl)=C1 LGXNQMGCMMSGAI-UHFFFAOYSA-N 0.000 description 1
XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
244000204909 Anoda cristata Species 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
235000019738 Limestone Nutrition 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000209504 Poaceae Species 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
239000007868 Raney catalyst Substances 0.000 description 1
NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
229910000564 Raney nickel Inorganic materials 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
ZKXKGPVPQDYNCY-UHFFFAOYSA-N [3-(ethoxycarbonylamino)phenyl] n-methyl-n-phenylcarbamate Chemical compound CCOC(=O)NC1=CC=CC(OC(=O)N(C)C=2C=CC=CC=2)=C1 ZKXKGPVPQDYNCY-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
150000008107 benzenesulfonic acids Chemical class 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
230000002708 enhancing effect Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 1
241001233957 eudicotyledons Species 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
RZILCCPWPBTYDO-UHFFFAOYSA-N fluometuron Chemical compound CN(C)C(=O)NC1=CC=CC(C(F)(F)F)=C1 RZILCCPWPBTYDO-UHFFFAOYSA-N 0.000 description 1
ISXSFOPKZQZDAO-UHFFFAOYSA-N formaldehyde;sodium Chemical compound [Na].O=C ISXSFOPKZQZDAO-UHFFFAOYSA-N 0.000 description 1
230000003179 granulation Effects 0.000 description 1
238000005469 granulation Methods 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000006028 limestone Substances 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
CPGWSLFYXMRNDV-UHFFFAOYSA-N n-methyl-n-phenylcarbamoyl chloride Chemical compound ClC(=O)N(C)C1=CC=CC=C1 CPGWSLFYXMRNDV-UHFFFAOYSA-N 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
210000002741 palatine tonsil Anatomy 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
239000002904 solvent Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
238000009333 weeding Methods 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

FI770488A 1976-02-27 1977-02-15 N-metylkarbanilsyra-(3-(etoxikarbonylamino)-fenyl)-ester anvaendbar som bomullherbicid FI59522C (fi)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19762608473 DE2608473A1 (de)	1976-02-27	1976-02-27	N-methylcarbanilsaeure- eckige klammer auf 3-(aethoxycarbonylamino)-phenyl eckige klammer zu -ester als baumwollherbizides mittel
DE2608473		1976-02-27

Publications (3)

Publication Number	Publication Date
FI770488A7 FI770488A7 (cs)	1977-08-28
FI59522B FI59522B (fi)	1981-05-29
FI59522C true FI59522C (fi)	1981-09-10

Family

ID=5971289

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI770488A FI59522C (fi)	1976-02-27	1977-02-15	N-metylkarbanilsyra-(3-(etoxikarbonylamino)-fenyl)-ester anvaendbar som bomullherbicid

Country Status (30)

Country	Link
US (1)	US4164414A (cs)
JP (1)	JPS605565B2 (cs)
AT (1)	AT350838B (cs)
AU (1)	AU502840B2 (cs)
BE (1)	BE851839A (cs)
BG (1)	BG27719A3 (cs)
BR (1)	BR7700416A (cs)
CA (1)	CA1097674A (cs)
CH (1)	CH626507A5 (cs)
CS (1)	CS191185B2 (cs)
DD (1)	DD128361A5 (cs)
DE (1)	DE2608473A1 (cs)
ES (1)	ES455243A1 (cs)
FI (1)	FI59522C (cs)
FR (1)	FR2342279A1 (cs)
GB (1)	GB1575815A (cs)
GR (1)	GR62396B (cs)
IL (1)	IL51462A (cs)
IN (1)	IN145579B (cs)
IT (1)	IT1075124B (cs)
MX (1)	MX4935E (cs)
NL (1)	NL7700134A (cs)
PH (1)	PH12878A (cs)
PL (1)	PL103048B1 (cs)
PT (1)	PT66209B (cs)
RO (1)	RO72553A (cs)
SE (1)	SE7701885L (cs)
TR (1)	TR20002A (cs)
YU (1)	YU977A (cs)
ZA (1)	ZA771150B (cs)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2310649C3 (de) *	1973-03-01	1982-05-06	Schering Ag, 1000 Berlin Und 4619 Bergkamen	Diurethane sowie diese enthaltende selektive herbizide Mittel
AU581532B2 (en) *	1985-06-27	1989-02-23	Diebold Incorporated	Control of document dispensing machine:
JPS62184591A (ja) *	1986-02-10	1987-08-12	オムロン株式会社	現金自動取引処理装置

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1567151C3 (de) *	1965-04-09	1974-02-21	Schering Ag, 1000 Berlin Und 4619 Bergkamen	Diurethane, Verfahren zur Herstellung dieser Verbindungen sowie diese enthaltende herbizide Mittel

1976
- 1976-02-27 DE DE19762608473 patent/DE2608473A1/de not_active Withdrawn
- 1976-12-29 AT AT975976A patent/AT350838B/de not_active IP Right Cessation
1977
- 1977-01-05 YU YU00009/77A patent/YU977A/xx unknown
- 1977-01-07 NL NL7700134A patent/NL7700134A/xx not_active Application Discontinuation
- 1977-01-18 CS CS77340A patent/CS191185B2/cs unknown
- 1977-01-21 ES ES455243A patent/ES455243A1/es not_active Expired
- 1977-01-24 BR BR7700416A patent/BR7700416A/pt unknown
- 1977-01-29 IN IN128/CAL/77A patent/IN145579B/en unknown
- 1977-02-03 MX MX775403U patent/MX4935E/es unknown
- 1977-02-04 RO RO7789275A patent/RO72553A/ro unknown
- 1977-02-07 BG BG035361A patent/BG27719A3/xx unknown
- 1977-02-09 CA CA271,416A patent/CA1097674A/en not_active Expired
- 1977-02-15 FI FI770488A patent/FI59522C/fi not_active IP Right Cessation
- 1977-02-16 IL IL51462A patent/IL51462A/xx unknown
- 1977-02-16 TR TR20002A patent/TR20002A/xx unknown
- 1977-02-18 PT PT66209A patent/PT66209B/pt unknown
- 1977-02-21 GB GB7193/77A patent/GB1575815A/en not_active Expired
- 1977-02-21 SE SE7701885A patent/SE7701885L/xx not_active Application Discontinuation
- 1977-02-22 US US05/770,492 patent/US4164414A/en not_active Expired - Lifetime
- 1977-02-23 CH CH225877A patent/CH626507A5/de not_active IP Right Cessation
- 1977-02-24 IT IT20654/77A patent/IT1075124B/it active
- 1977-02-24 PH PH19492A patent/PH12878A/en unknown
- 1977-02-25 ZA ZA00771150A patent/ZA771150B/xx unknown
- 1977-02-25 PL PL1977196268A patent/PL103048B1/pl unknown
- 1977-02-25 GR GR52855A patent/GR62396B/el unknown
- 1977-02-25 BE BE175269A patent/BE851839A/xx not_active IP Right Cessation
- 1977-02-25 DD DD7700197571A patent/DD128361A5/xx unknown
- 1977-02-28 FR FR7705759A patent/FR2342279A1/fr active Granted
- 1977-02-28 JP JP52021395A patent/JPS605565B2/ja not_active Expired
- 1977-02-28 AU AU22754/77A patent/AU502840B2/en not_active Expired

Also Published As

Publication number	Publication date
JPS605565B2 (ja)	1985-02-12
FI770488A7 (cs)	1977-08-28
CA1097674A (en)	1981-03-17
CS191185B2 (en)	1979-06-29
JPS52105215A (en)	1977-09-03
DD128361A5 (de)	1977-11-16
ES455243A1 (es)	1977-12-16
RO72553A (ro)	1982-09-09
IT1075124B (it)	1985-04-22
PL103048B1 (pl)	1979-05-31
ATA975976A (de)	1978-11-15
DE2608473A1 (de)	1977-09-01
AT350838B (de)	1979-06-25
PH12878A (en)	1979-09-25
MX4935E (es)	1983-01-05
GR62396B (en)	1979-04-10
SE7701885L (sv)	1977-08-28
FR2342279B1 (cs)	1981-07-03
AU2275477A (en)	1978-09-07
CH626507A5 (cs)	1981-11-30
AU502840B2 (en)	1979-08-09
ZA771150B (en)	1978-01-25
PT66209B (de)	1978-07-12
PT66209A (de)	1977-03-01
FI59522B (fi)	1981-05-29
BR7700416A (pt)	1977-09-20
NL7700134A (nl)	1977-08-30
GB1575815A (en)	1980-10-01
US4164414A (en)	1979-08-14
TR20002A (tr)	1980-06-10
BG27719A3 (bg)	1979-12-12
YU977A (en)	1982-10-31
IN145579B (cs)	1985-01-05
BE851839A (fr)	1977-08-25
IL51462A0 (en)	1977-04-29
IL51462A (en)	1981-10-30
FR2342279A1 (fr)	1977-09-23

Legal Events

Date	Code	Title	Description
2004-08-31	MM	Patent lapsed	Owner name: SCHERING AKTIENGESELLSCHAFT

Publication	Publication Date	Title
US4134751A (en)	1979-01-16	Herbicidal compound, herbicidal composition containing the same and method of use thereof
KR840001968B1 (ko)	1984-10-26	옥심 유도체의 제조방법
CS207776B2 (en)	1981-08-31	Herbicide means
KR920000050B1 (ko)	1992-01-06	2-치환 페닐-3-클로로테트라히드로-2h-인다졸류의 제조방법
FI59522C (fi)	1981-09-10	N-metylkarbanilsyra-(3-(etoxikarbonylamino)-fenyl)-ester anvaendbar som bomullherbicid
EP0135838B1 (de)	1990-04-18	3-Phenyl-4-methoxycarbonylpyrazole, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
RU2056413C1 (ru)	1996-03-20	Иминотиазолины, способы их получения, гербицидная композиция, способ уничтожения нежелательных сорняков
US4258038A (en)	1981-03-24	Unsymmetrical thiophosphonate insecticides and nematocides
DE2413597A1 (de)	1974-10-03	Verfahren zur herstellung von phosphorsaeureestern
EP0493321A1 (de)	1992-07-01	Pyrimidinyl- und Triazinyl-salicylamide sowie deren Verwendung und Herstellung
KR910006448B1 (ko)	1991-08-26	복소환 화합물, 그의 제조방법 및 그를 유효성분으로서 함유하는 제초제 조성물
CS210629B2 (en)	1982-01-29	Herbicide
AU604911B2 (en)	1991-01-03	Herbicidal thiocarboxylic acid derivatives
US3890385A (en)	1975-06-17	Dichlorobenzaldehyde-oxime-carbonates
US4758263A (en)	1988-07-19	2-(2,5-difluorophenyl)-4-methyl-1,2,4-oxadiazolidine-3,5 diones
EP0249858B1 (de)	1990-12-05	Fluoralkylsubstituierte Chinolinderivate. ihre Herstellung sowie Verwendung zur Bekämpfung unerwünschten Pflanzenwachstums
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