NO742394L - - Google Patents

Info

Publication number: NO742394L
Authority: NO; Norway
Prior art keywords: residue; alkyl; dinitro; propyl; trifluoromethylaniline
Prior art date: 1973-07-07

Application number

NO742394A

Other languages

English (en)

Norwegian (no)

Inventor

A Fischer

Original Assignee

Basf 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.)

1973-07-07

Filing date

1974-07-01

Publication date

1975-02-03

1974-07-01 Application filed by Basf Ag filed Critical Basf Ag

1975-02-03 Publication of NO742394L publication Critical patent/NO742394L/no

Links

239000000203 mixture Substances 0.000 claims description 31
-1 methoxy, amino- sulfonyl Chemical group 0.000 claims description 16
150000001875 compounds Chemical class 0.000 claims description 13
230000002363 herbicidal effect Effects 0.000 claims description 12
125000000217 alkyl group Chemical group 0.000 claims description 11
239000004009 herbicide Substances 0.000 claims description 9
125000003342 alkenyl group Chemical group 0.000 claims description 8
229910052736 halogen Inorganic materials 0.000 claims description 8
150000002367 halogens Chemical group 0.000 claims description 8
125000000304 alkynyl group Chemical group 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 6
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 5
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
239000005864 Sulphur Substances 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 4
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
125000001188 haloalkyl group Chemical group 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
239000001301 oxygen Substances 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
125000001931 aliphatic group Chemical group 0.000 claims description 2
125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
239000000460 chlorine Substances 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims description 2
241000282994 Cervidae Species 0.000 claims 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
125000000753 cycloalkyl group Chemical group 0.000 claims 1
125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 1
239000013543 active substance Substances 0.000 description 26
241000196324 Embryophyta Species 0.000 description 23
239000000126 substance Substances 0.000 description 16
150000002148 esters Chemical class 0.000 description 10
239000003795 chemical substances by application Substances 0.000 description 9
239000003921 oil Substances 0.000 description 9
239000002253 acid Substances 0.000 description 8
239000002689 soil Substances 0.000 description 8
239000006185 dispersion Substances 0.000 description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
239000000839 emulsion Substances 0.000 description 6
239000008187 granular material Substances 0.000 description 6
230000000694 effects Effects 0.000 description 4
239000000843 powder Substances 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000003513 alkali Substances 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
125000004494 ethyl ester group Chemical group 0.000 description 3
150000002790 naphthalenes Chemical class 0.000 description 3
239000006072 paste Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
ODGIMMLDVSWADK-UHFFFAOYSA-N 4-trifluoromethylaniline Chemical compound NC1=CC=C(C(F)(F)F)C=C1 ODGIMMLDVSWADK-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
239000012876 carrier material Substances 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000000428 dust Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
230000012010 growth Effects 0.000 description 2
239000002917 insecticide Substances 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
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 2
239000002574 poison Substances 0.000 description 2
231100000614 poison Toxicity 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
235000021067 refined food Nutrition 0.000 description 2
239000000741 silica gel Substances 0.000 description 2
229910002027 silica gel Inorganic materials 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
238000009736 wetting Methods 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical class OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 description 1
QZEDXQFZACVDJE-UHFFFAOYSA-N 2,3-dibutylnaphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(O)(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 QZEDXQFZACVDJE-UHFFFAOYSA-N 0.000 description 1
CGNBQYFXGQHUQP-UHFFFAOYSA-N 2,3-dinitroaniline Chemical class NC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O CGNBQYFXGQHUQP-UHFFFAOYSA-N 0.000 description 1
PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical class CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
244000105624 Arachis hypogaea Species 0.000 description 1
235000010777 Arachis hypogaea Nutrition 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
241000245654 Gladiolus Species 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
244000299507 Gossypium hirsutum Species 0.000 description 1
235000009432 Gossypium hirsutum Nutrition 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241000209510 Liliopsida Species 0.000 description 1
235000019738 Limestone Nutrition 0.000 description 1
101100523604 Mus musculus Rassf5 gene Proteins 0.000 description 1
GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
240000004713 Pisum sativum Species 0.000 description 1
235000010582 Pisum sativum Nutrition 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
244000025012 Spondias pinnata Species 0.000 description 1
235000005658 Spondias pinnata Nutrition 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000032683 aging Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000005215 alkyl ethers Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
235000021028 berry Nutrition 0.000 description 1
210000000081 body of the sternum Anatomy 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000011280 coal tar Substances 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
239000002283 diesel fuel Substances 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000009826 distribution Methods 0.000 description 1
239000012990 dithiocarbamate Substances 0.000 description 1
150000004659 dithiocarbamates Chemical class 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
UTXTVFKBKYJAMA-UHFFFAOYSA-N ethyl N-(1-bicyclo[2.2.1]heptanyl)-N-ethylcarbamodithioate Chemical compound C(C)SC(N(C12CCC(CC1)C2)CC)=S UTXTVFKBKYJAMA-UHFFFAOYSA-N 0.000 description 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
241001233957 eudicotyledons Species 0.000 description 1
239000000194 fatty acid Chemical class 0.000 description 1
229930195729 fatty acid Chemical class 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000011888 foil Substances 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N heptadecan-1-ol Chemical class CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical class CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 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
239000003350 kerosene Substances 0.000 description 1
239000004571 lime Substances 0.000 description 1
239000006028 limestone Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
KXHORCXSQZTQQI-UHFFFAOYSA-N n-(fluoromethyl)aniline Chemical compound FCNC1=CC=CC=C1 KXHORCXSQZTQQI-UHFFFAOYSA-N 0.000 description 1
SLFVYFOEHHLHDW-UHFFFAOYSA-N n-(trifluoromethyl)aniline Chemical compound FC(F)(F)NC1=CC=CC=C1 SLFVYFOEHHLHDW-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
HLLYDGVOMRCOFR-UHFFFAOYSA-N n-butyl-n-ethyl-2,6-dinitro-4-(trifluoromethyl)aniline;2,6-dinitro-n,n-dipropyl-4-(trifluoromethyl)aniline Chemical compound CCCCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O.CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O HLLYDGVOMRCOFR-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
239000005416 organic matter Substances 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
125000005624 silicic acid group Chemical class 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003892 spreading Methods 0.000 description 1
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
235000012222 talc Nutrition 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000011269 tar Substances 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
239000011573 trace mineral Substances 0.000 description 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 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
- G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
- G03H1/04—Processes or apparatus for producing holograms

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

NO742394A 1973-07-07 1974-07-01 NO742394L (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19732334563 DE2334563A1 (de)	1973-07-07	1973-07-07	Herbizid

Publications (1)

Publication Number	Publication Date
NO742394L true NO742394L (fr)	1975-02-03

Family

ID=5886189

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO742394A NO742394L (fr)	1973-07-07	1974-07-01

Country Status (24)

Country	Link
JP (1)	JPS5036636A (fr)
AR (1)	AR217032A1 (fr)
BE (1)	BE817305A (fr)
BG (2)	BG22056A3 (fr)
BR (1)	BR7405534D0 (fr)
CH (1)	CH585005A5 (fr)
CS (1)	CS189658B2 (fr)
DD (1)	DD111778A5 (fr)
DE (1)	DE2334563A1 (fr)
DK (1)	DK137742C (fr)
ES (1)	ES428035A1 (fr)
FR (1)	FR2235645B1 (fr)
GB (1)	GB1471772A (fr)
HU (1)	HU169820B (fr)
IL (1)	IL45060A (fr)
IT (1)	IT1049296B (fr)
LU (1)	LU70472A1 (fr)
NL (1)	NL7409071A (fr)
NO (1)	NO742394L (fr)
PL (1)	PL94007B1 (fr)
RO (1)	RO69333A (fr)
SE (1)	SE7408882L (fr)
SU (1)	SU579844A3 (fr)
ZA (1)	ZA744217B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5520919A (en) *	1978-07-31	1980-02-14	Nihon Radiator Co	Parts connecting method to aluminium pipe
DE2909158A1 (de) *	1979-03-08	1980-09-11	Basf Ag	Herbizide mischungen
PT82293B (en) *	1985-04-08	1988-01-11	Stauffer Chemical Co	Process for the preparation of synergetic herbicide compositions containing a tiolcarbamate and a by product with benzene

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3449111A (en) *	1966-12-08	1969-06-10	Lilly Co Eli	Method of eliminating weeds
US3518076A (en) *	1967-05-17	1970-06-30	Lilly Co Eli	Method of fliminating weed species with herbicidal combination

1973
- 1973-07-07 DE DE19732334563 patent/DE2334563A1/de not_active Withdrawn
1974
- 1974-06-17 BG BG26996A patent/BG22056A3/xx unknown
- 1974-06-17 BG BG028827A patent/BG25636A3/xx unknown
- 1974-06-17 AR AR254225A patent/AR217032A1/es active
- 1974-06-18 IL IL45060A patent/IL45060A/en unknown
- 1974-06-25 JP JP49071970A patent/JPS5036636A/ja active Pending
- 1974-06-28 RO RO7479338A patent/RO69333A/fr unknown
- 1974-07-01 NO NO742394A patent/NO742394L/no unknown
- 1974-07-01 ZA ZA00744217A patent/ZA744217B/xx unknown
- 1974-07-04 FR FR7423307A patent/FR2235645B1/fr not_active Expired
- 1974-07-04 NL NL7409071A patent/NL7409071A/xx not_active Application Discontinuation
- 1974-07-04 BR BR5534/74A patent/BR7405534D0/pt unknown
- 1974-07-05 DK DK361174A patent/DK137742C/da not_active IP Right Cessation
- 1974-07-05 PL PL1974172460A patent/PL94007B1/pl unknown
- 1974-07-05 BE BE146264A patent/BE817305A/fr unknown
- 1974-07-05 SE SE7408882A patent/SE7408882L/xx unknown
- 1974-07-05 CS CS744807A patent/CS189658B2/cs unknown
- 1974-07-05 LU LU70472A patent/LU70472A1/xx unknown
- 1974-07-05 SU SU7402042434A patent/SU579844A3/ru active
- 1974-07-05 HU HUBA3109A patent/HU169820B/hu unknown
- 1974-07-05 CH CH926774A patent/CH585005A5/xx not_active IP Right Cessation
- 1974-07-05 GB GB2987074A patent/GB1471772A/en not_active Expired
- 1974-07-05 IT IT51942/74A patent/IT1049296B/it active
- 1974-07-05 DD DD179738A patent/DD111778A5/xx unknown
- 1974-07-06 ES ES428035A patent/ES428035A1/es not_active Expired

Also Published As

Publication number	Publication date
SU579844A3 (ru)	1977-11-05
LU70472A1 (fr)	1974-11-28
JPS5036636A (fr)	1975-04-05
BE817305A (fr)	1975-01-06
HU169820B (fr)	1977-02-28
DE2334563A1 (de)	1975-01-30
CH585005A5 (fr)	1977-02-28
AU7028774A (en)	1976-01-08
IL45060A0 (en)	1974-09-10
RO69333A (fr)	1980-06-15
FR2235645A1 (fr)	1975-01-31
BR7405534D0 (pt)	1975-05-06
IL45060A (en)	1977-10-31
BG22056A3 (fr)	1976-11-25
IT1049296B (it)	1981-01-20
DK361174A (fr)	1975-02-24
SE7408882L (fr)	1975-01-08
ES428035A1 (es)	1977-02-01
DK137742C (da)	1978-10-09
DK137742B (da)	1978-05-01
BG25636A3 (bg)	1978-11-10
PL94007B1 (fr)	1977-07-30
GB1471772A (en)	1977-04-27
ZA744217B (en)	1975-08-27
FR2235645B1 (fr)	1978-07-07
NL7409071A (nl)	1975-01-09
CS189658B2 (en)	1979-04-30
AR217032A1 (es)	1980-02-29
DD111778A5 (fr)	1975-03-12

Publication	Publication Date	Title
EP0090309A1 (fr)	1983-10-05	Esters d'acide dihydrothiophène-carboxylique, procédé pour les préparer et leur application à la lutte de la croissance indésirable des plantes
EP0329012A2 (fr)	1989-08-23	Naphthyridine et Pyridopyrimidine Sulfonamides
EP0003805B1 (fr)	1982-06-30	Pyridazones et compositions herbicides les contenant
EP0334120A1 (fr)	1989-09-27	Isoxazolines, procédé de préparation et utilisation
EP0031042B1 (fr)	1983-01-26	Dérivés de N-dichloroacétyldiazabicyclo, procédé pour leur préparation, herbicides contenant des acétanilides comme herbicides et ces dérives de N-dichloroacétyldiazabicyclo comme antidotes et leur utilisation pour la lutte contre la végétation indésirable
EP0116932A1 (fr)	1984-08-29	Esters d'acide thiophène-carboxylique, procédé pour leur préparation et leur application comme herbicides
DE2219923C3 (de)	1979-07-05	Substituierte O- [Aminosulfonyl] -glykolsäureamide
NO742394L (fr)	1975-02-03
EP0065724B1 (fr)	1984-08-08	Dihalogénoacétamides, procédé pour leur préparation et herbicides contenant acétanilides comme herbicides et dihalogénoacétamides comme antidotes
PL89177B1 (en)	1976-10-30	Synergistic herbicidal mixture[us3888655a]
EP0135838B1 (fr)	1990-04-18	3-Phényl-4-méthoxy carbonylepyrazoles, leur procédé de préparation et leur utilisation dans la lutte contre la croissance de plantes indésirables
DE2711230A1 (de)	1977-09-29	N-(4-benzyloxyphenyl)-n'-methyl-n'- methoxyharnstoff, verfahren zu seiner herstellung und seine verwendung als herbizid insbesondere in sojabohnenkulturen
EP0036390A2 (fr)	1981-09-23	Diphényléther-urées à propriétés herbicides
EP0013873B1 (fr)	1982-01-20	Anilides de l'acide N-azolyl acétique, procédé pour leur préparation et leur utilisation comme herbicides
EP0001271B1 (fr)	1982-10-27	Dérivés hétérocycliques de norbornane, agents régulateurs de la croissance des plantes contenant ces composés et procédé pour la préparation de ces agents
KR920001304B1 (ko)	1992-02-10	에폭사이드 제초제
EP0084673B1 (fr)	1986-04-02	Aminothiadiazoles, leur procédé de synthèse et leur application dans la lutte contre les mauvaises herbes
HU181849B (en)	1983-11-28	Synergetic herbicide composition containing a mixture of acetanilides
EP0078462B1 (fr)	1986-01-15	1,2,4,6-Thiatriazin-1,1-dioxydes, leur procédé de préparation et leur application à la lutte contre la croissance des mauvaises herbes
EP0107123B1 (fr)	1987-07-01	Dérivés d'aniline, procédé pour leur préparation et leur utilisation dans la lutte contre la croissance des plantes indésirables
EP0216299A1 (fr)	1987-04-01	Dérivés de la quinoxaline, leur procédé de préparation et leur utilisation pour protéger les plantes cultivées contre l'effet phytotoxique d'herbicides
EP0098972A2 (fr)	1984-01-25	Dérivés de 5-(4' ureido)-phénoxy benzisothiazole, procédé pour les préparer et leur utilisation comme herbicides
US3975179A (en)	1976-08-17	Herbicide mixtures of 3-lower alkyl-2,1,3-benzothiadiazinone-(4)-2,2-dioxides and thiazoles
EP0007588A1 (fr)	1980-02-06	Tétrahydro-1,3-oxazines, compositions herbicides contenant des acétanilides comme agents herbicides et ces tétrahydro-1,3-oxazines comme agents antagonistes et leur application pour la lutte contre la croissance indésirable de plantes
EP0037482A2 (fr)	1981-10-14	3,4,5,6-Tétrahydro-1,2,4,6-thiatriazine(3,5)dione-1,1-dioxides, leur préparation, les herbicides les contenant, procédé de préparation d'herbicides et procédé pour la lutte contre la croissance de la végétation indésirable