NO742407L - - Google Patents

Info

Publication number: NO742407L
Authority: NO; Norway
Prior art keywords: substituted; acetanilido; weight; parts; methyl
Prior art date: 1973-07-07

Application number

NO742407A

Other languages

English (en)

Norwegian (no)

Inventor

A Fischer

H Hansen

W Rohr

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

1974-07-02

Publication date

1975-02-03

1974-07-02 Application filed by Basf Ag filed Critical Basf Ag

1975-02-03 Publication of NO742407L publication Critical patent/NO742407L/no

Links

-1 Sulfuric acid esters aromatic glycolic acid amides Chemical class 0.000 claims description 28
125000001931 aliphatic group Chemical group 0.000 claims description 7
230000002363 herbicidal effect Effects 0.000 claims description 7
229910052736 halogen Inorganic materials 0.000 claims description 6
150000002367 halogens Chemical class 0.000 claims description 6
239000004009 herbicide Substances 0.000 claims description 6
125000003545 alkoxy group Chemical group 0.000 claims description 5
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 3
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims 4
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 4
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
150000003839 salts Chemical class 0.000 description 23
239000013543 active substance Substances 0.000 description 18
150000002148 esters Chemical class 0.000 description 17
150000001408 amides Chemical class 0.000 description 16
239000000126 substance Substances 0.000 description 12
241000196324 Embryophyta Species 0.000 description 11
239000003921 oil Substances 0.000 description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
239000000203 mixture Substances 0.000 description 10
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
239000003795 chemical substances by application Substances 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
239000002253 acid Substances 0.000 description 8
150000001875 compounds Chemical class 0.000 description 8
239000006185 dispersion Substances 0.000 description 8
238000002360 preparation method Methods 0.000 description 6
239000000047 product Substances 0.000 description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
150000007513 acids Chemical class 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
239000004359 castor oil Substances 0.000 description 4
235000019438 castor oil Nutrition 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000007787 solid Substances 0.000 description 4
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
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000003513 alkali Substances 0.000 description 3
239000012876 carrier material Substances 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
239000000499 gel Substances 0.000 description 3
239000008187 granular material Substances 0.000 description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
238000002156 mixing Methods 0.000 description 3
150000002790 naphthalenes Chemical class 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
235000012239 silicon dioxide Nutrition 0.000 description 3
239000002904 solvent Substances 0.000 description 3
235000013311 vegetables Nutrition 0.000 description 3
NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical class CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 2
125000006179 2-methyl benzyl group Chemical group [H]C1=C([H])C(=C(C([H])=C1[H])C([H])([H])*)C([H])([H])[H] 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 2
239000005995 Aluminium silicate Substances 0.000 description 2
241000219193 Brassicaceae Species 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
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
241000219071 Malvaceae Species 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
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
241000013557 Plantaginaceae Species 0.000 description 2
235000004789 Rosa xanthina Nutrition 0.000 description 2
241000220222 Rosaceae Species 0.000 description 2
241000208292 Solanaceae Species 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
230000000844 anti-bacterial effect Effects 0.000 description 2
239000003899 bactericide agent Substances 0.000 description 2
238000009835 boiling Methods 0.000 description 2
125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
125000000480 butynyl group Chemical group [*]C#CC([H])([H])C([H])([H])[H] 0.000 description 2
235000013339 cereals Nutrition 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
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
239000003630 growth substance Substances 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
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 2
238000004519 manufacturing process Methods 0.000 description 2
239000000463 material Substances 0.000 description 2
238000000034 method Methods 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
230000001069 nematicidal effect Effects 0.000 description 2
239000005645 nematicide Substances 0.000 description 2
YDCVQGAUCOROHB-UHFFFAOYSA-N oxadiazolidine-4,5-dione Chemical class O=C1NNOC1=O YDCVQGAUCOROHB-UHFFFAOYSA-N 0.000 description 2
239000006072 paste Substances 0.000 description 2
230000008635 plant growth Effects 0.000 description 2
NYCVCXMSZNOGDH-UHFFFAOYSA-N pyrrolidine-1-carboxylic acid Chemical class OC(=O)N1CCCC1 NYCVCXMSZNOGDH-UHFFFAOYSA-N 0.000 description 2
150000003235 pyrrolidines Chemical class 0.000 description 2
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
239000000741 silica gel Substances 0.000 description 2
229910002027 silica gel Inorganic materials 0.000 description 2
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
239000002689 soil Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 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
239000008096 xylene Substances 0.000 description 2
FTDGDIFUDKDKAW-UHFFFAOYSA-N 1,1a,5,5a,6,6a-hexahydrocyclopropa[a]indene Chemical class C12C(CC3CC=CC=C13)C2 FTDGDIFUDKDKAW-UHFFFAOYSA-N 0.000 description 1
FNQJDLTXOVEEFB-UHFFFAOYSA-N 1,2,3-benzothiadiazole Chemical class C1=CC=C2SN=NC2=C1 FNQJDLTXOVEEFB-UHFFFAOYSA-N 0.000 description 1
CSNIZNHTOVFARY-UHFFFAOYSA-N 1,2-benzothiazole Chemical class C1=CC=C2C=NSC2=C1 CSNIZNHTOVFARY-UHFFFAOYSA-N 0.000 description 1
VPGSXIKVUASQIY-UHFFFAOYSA-N 1,2-dibutylnaphthalene Chemical class C1=CC=CC2=C(CCCC)C(CCCC)=CC=C21 VPGSXIKVUASQIY-UHFFFAOYSA-N 0.000 description 1
MFVFDTCSVFBOTL-UHFFFAOYSA-N 1,3-diazetidine Chemical class C1NCN1 MFVFDTCSVFBOTL-UHFFFAOYSA-N 0.000 description 1
HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 1
FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 description 1
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
PNEABRNAYDDYJK-UHFFFAOYSA-N 2-hydroxy-n-methyl-n-phenylacetamide Chemical compound OCC(=O)N(C)C1=CC=CC=C1 PNEABRNAYDDYJK-UHFFFAOYSA-N 0.000 description 1
TZGPACAKMCUCKX-UHFFFAOYSA-N 2-hydroxyacetamide Chemical class NC(=O)CO TZGPACAKMCUCKX-UHFFFAOYSA-N 0.000 description 1
UOCUSOBVEHOMMB-UHFFFAOYSA-N 2h-1$l^{6},2,3-benzothiadiazine 1,1-dioxide Chemical class C1=CC=C2S(=O)(=O)NN=CC2=C1 UOCUSOBVEHOMMB-UHFFFAOYSA-N 0.000 description 1
125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 description 1
241000219479 Aizoaceae Species 0.000 description 1
241000234282 Allium Species 0.000 description 1
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244000099147 Ananas comosus Species 0.000 description 1
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LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
241001072256 Boraginaceae Species 0.000 description 1
241000234670 Bromeliaceae Species 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
WUFYJSIFTHYAGJ-UHFFFAOYSA-N C=1C=NSC=1.O=C1N=CC=CN1 Chemical class C=1C=NSC=1.O=C1N=CC=CN1 WUFYJSIFTHYAGJ-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
241000219321 Caryophyllaceae Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 description 1
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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
241000551547 Dione <red algae> Species 0.000 description 1
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PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
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244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
244000299507 Gossypium hirsutum Species 0.000 description 1
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UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
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241000234280 Liliaceae Species 0.000 description 1
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235000019738 Limestone Nutrition 0.000 description 1
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SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
FIWILGQIZHDAQG-UHFFFAOYSA-N NC1=C(C(=O)NCC2=CC=C(C=C2)OCC(F)(F)F)C=C(C(=N1)N)N1N=C(N=C1)C1(CC1)C(F)(F)F Chemical compound NC1=C(C(=O)NCC2=CC=C(C=C2)OCC(F)(F)F)C=C(C(=N1)N)N1N=C(N=C1)C1(CC1)C(F)(F)F FIWILGQIZHDAQG-UHFFFAOYSA-N 0.000 description 1
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239000005662 Paraffin oil Substances 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
241000209504 Poaceae Species 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
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241000208476 Primulaceae Species 0.000 description 1
WTKZEGDFNFYCGP-UHFFFAOYSA-O Pyrazolium Chemical class C1=CN[NH+]=C1 WTKZEGDFNFYCGP-UHFFFAOYSA-O 0.000 description 1
241001107098 Rubiaceae Species 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
239000005659 Urtica spp. Substances 0.000 description 1
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241000159213 Zygophyllaceae Species 0.000 description 1
229960001413 acetanilide Drugs 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates 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
150000003863 ammonium salts Chemical class 0.000 description 1
125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
230000002303 anti-venom Effects 0.000 description 1
239000000729 antidote Substances 0.000 description 1
229940075522 antidotes Drugs 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
BUSBFZWLPXDYIC-UHFFFAOYSA-N arsonic acid Chemical class O[AsH](O)=O BUSBFZWLPXDYIC-UHFFFAOYSA-N 0.000 description 1
150000005130 benzoxazines Chemical class 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
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OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
235000013877 carbamide Nutrition 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
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DNTYXOAEBUZAJC-UHFFFAOYSA-N chlorosulfinyloxyethane Chemical compound CCOS(Cl)=O DNTYXOAEBUZAJC-UHFFFAOYSA-N 0.000 description 1
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239000011280 coal tar Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
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150000001991 dicarboxylic acids Chemical group 0.000 description 1
239000002283 diesel fuel Substances 0.000 description 1
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238000009826 distribution Methods 0.000 description 1
150000002019 disulfides Chemical class 0.000 description 1
239000012990 dithiocarbamate Substances 0.000 description 1
150000004659 dithiocarbamates Chemical class 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
QQSGDKKFXBGYON-UHFFFAOYSA-N ethoxy-methylperoxy-(6-methyl-2-propan-2-ylpyrimidin-4-yl)oxy-sulfanylidene-$l^{5}-phosphane Chemical class CCOP(=S)(OOC)OC1=CC(C)=NC(C(C)C)=N1 QQSGDKKFXBGYON-UHFFFAOYSA-N 0.000 description 1
NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
VOTNXLNTNMCSTJ-UHFFFAOYSA-N ethyl hydrogen sulfite Chemical compound CCOS(O)=O VOTNXLNTNMCSTJ-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
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150000004665 fatty acids Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
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229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
150000002333 glycines Chemical class 0.000 description 1
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125000001188 haloalkyl group Chemical group 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
150000001469 hydantoins Chemical class 0.000 description 1
229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
150000002460 imidazoles Chemical class 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
150000002545 isoxazoles Chemical class 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000004571 lime Substances 0.000 description 1
239000006028 limestone Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000010807 litter Substances 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 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
150000002791 naphthoquinones Chemical class 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
QNMLMAVEXUCXRG-UHFFFAOYSA-N oxadiazinane-4,5-dione Chemical class O=C1CONNC1=O QNMLMAVEXUCXRG-UHFFFAOYSA-N 0.000 description 1
SDRLFDJOSQLRPB-UHFFFAOYSA-N oxadiazine-4,5-dione Chemical class O=C1CON=NC1=O SDRLFDJOSQLRPB-UHFFFAOYSA-N 0.000 description 1
150000004866 oxadiazoles Chemical class 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
REJGOFYVRVIODZ-UHFFFAOYSA-N phosphanium;chloride Chemical class P.Cl REJGOFYVRVIODZ-UHFFFAOYSA-N 0.000 description 1
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
150000003009 phosphonic acids Chemical class 0.000 description 1
235000011007 phosphoric acid Nutrition 0.000 description 1
150000003016 phosphoric acids Chemical class 0.000 description 1
SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical class OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 1
150000003053 piperidines Chemical class 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920000056 polyoxyethylene ether Polymers 0.000 description 1
229940051841 polyoxyethylene ether Drugs 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 1
150000005299 pyridinones Chemical class 0.000 description 1
150000003230 pyrimidines Chemical class 0.000 description 1
150000008318 pyrimidones Chemical class 0.000 description 1
150000004040 pyrrolidinones Chemical class 0.000 description 1
150000003246 quinazolines Chemical class 0.000 description 1
150000003248 quinolines Chemical group 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
125000005624 silicic acid group Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003892 spreading Methods 0.000 description 1
125000003011 styrenyl group Chemical class [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
125000001424 substituent group Chemical group 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
229910052623 talc Inorganic materials 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
OLPRIZQBWZMBAS-UHFFFAOYSA-N thiadiazolidine 1,1-dioxide Chemical class O=S1(=O)CCNN1 OLPRIZQBWZMBAS-UHFFFAOYSA-N 0.000 description 1
150000003566 thiocarboxylic acids Chemical class 0.000 description 1
150000003582 thiophosphoric acids Chemical class 0.000 description 1
150000003585 thioureas Chemical class 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
244000045561 useful plants Species 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C305/00—Esters of sulfuric acids
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C301/00—Esters of sulfurous acid

Landscapes

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

NO742407A 1973-07-07 1974-07-02 NO742407L (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19732334715 DE2334715A1 (de)	1973-07-07	1973-07-07	Schwefligsaeureester aromatischer glykolsaeureamide

Publications (1)

Publication Number	Publication Date
NO742407L true NO742407L (fr)	1975-02-03

Family

ID=5886296

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO742407A NO742407L (fr)	1973-07-07	1974-07-02

Country Status (27)

Country	Link
US (1)	US4001292A (fr)
JP (1)	JPS5036628A (fr)
AR (1)	AR208670A1 (fr)
AT (1)	AT335791B (fr)
BE (1)	BE817307A (fr)
BG (1)	BG21583A3 (fr)
BR (1)	BR7405566D0 (fr)
CA (1)	CA1029738A (fr)
CH (1)	CH585009A5 (fr)
CS (1)	CS187419B2 (fr)
DD (1)	DD112208A5 (fr)
DE (1)	DE2334715A1 (fr)
DK (1)	DK361574A (fr)
FR (1)	FR2235916B1 (fr)
GB (1)	GB1466277A (fr)
HU (1)	HU168173B (fr)
IL (1)	IL45165A (fr)
IT (1)	IT1049298B (fr)
LU (1)	LU70474A1 (fr)
NL (1)	NL7408959A (fr)
NO (1)	NO742407L (fr)
PH (1)	PH10836A (fr)
PL (1)	PL88542B1 (fr)
SE (1)	SE7408884L (fr)
SU (1)	SU550955A3 (fr)
YU (2)	YU185574A (fr)
ZA (1)	ZA744337B (fr)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2917502A (en) *	1956-01-26	1959-12-15	Ciba Pharm Prod Inc	Process for the manufacture of amino carboxylic acid esters and peptide reactants therefor

1973
- 1973-07-07 DE DE19732334715 patent/DE2334715A1/de active Pending
1974
- 1974-06-26 BG BG27084A patent/BG21583A3/xx unknown
- 1974-07-01 IL IL45165A patent/IL45165A/en unknown
- 1974-07-01 US US05/484,419 patent/US4001292A/en not_active Expired - Lifetime
- 1974-07-02 NO NO742407A patent/NO742407L/no unknown
- 1974-07-02 NL NL7408959A patent/NL7408959A/xx not_active Application Discontinuation
- 1974-07-02 YU YU01855/74A patent/YU185574A/xx unknown
- 1974-07-02 YU YU01855/79A patent/YU185579A/xx unknown
- 1974-07-04 JP JP49075914A patent/JPS5036628A/ja active Pending
- 1974-07-04 DD DD179701A patent/DD112208A5/xx unknown
- 1974-07-04 CA CA204,044A patent/CA1029738A/fr not_active Expired
- 1974-07-05 LU LU70474A patent/LU70474A1/xx unknown
- 1974-07-05 PL PL1974172459A patent/PL88542B1/pl unknown
- 1974-07-05 BE BE146266A patent/BE817307A/fr unknown
- 1974-07-05 IT IT51947/74A patent/IT1049298B/it active
- 1974-07-05 SE SE7408884A patent/SE7408884L/xx not_active Application Discontinuation
- 1974-07-05 GB GB2987474A patent/GB1466277A/en not_active Expired
- 1974-07-05 SU SU2044346A patent/SU550955A3/ru active
- 1974-07-05 HU HUBA3107A patent/HU168173B/hu unknown
- 1974-07-05 BR BR5566/74A patent/BR7405566D0/pt unknown
- 1974-07-05 DK DK361574A patent/DK361574A/da unknown
- 1974-07-05 CS CS744806A patent/CS187419B2/cs unknown
- 1974-07-05 AR AR254564A patent/AR208670A1/es active
- 1974-07-05 PH PH16015A patent/PH10836A/en unknown
- 1974-07-05 AT AT557074A patent/AT335791B/de not_active IP Right Cessation
- 1974-07-05 CH CH927074A patent/CH585009A5/xx not_active IP Right Cessation
- 1974-07-05 ZA ZA00744337A patent/ZA744337B/xx unknown
- 1974-07-05 FR FR7423490A patent/FR2235916B1/fr not_active Expired

Also Published As

Publication number	Publication date
FR2235916A1 (fr)	1975-01-31
HU168173B (fr)	1976-03-28
GB1466277A (en)	1977-03-02
DE2334715A1 (de)	1975-01-30
LU70474A1 (fr)	1974-11-28
BG21583A3 (fr)	1976-07-20
ZA744337B (en)	1975-08-27
ATA557074A (de)	1976-07-15
CS187419B2 (en)	1979-01-31
PL88542B1 (fr)	1976-09-30
AU7095074A (en)	1976-01-08
SU550955A3 (ru)	1977-03-15
IT1049298B (it)	1981-01-20
FR2235916B1 (fr)	1977-10-07
AR208670A1 (es)	1977-02-28
JPS5036628A (fr)	1975-04-05
PH10836A (en)	1977-09-09
DK361574A (fr)	1975-03-03
AT335791B (de)	1977-03-25
BR7405566D0 (pt)	1975-05-06
BE817307A (fr)	1975-01-06
CH585009A5 (fr)	1977-02-28
CA1029738A (fr)	1978-04-18
SE7408884L (fr)	1975-01-08
US4001292A (en)	1977-01-04
DD112208A5 (fr)	1975-04-05
NL7408959A (nl)	1975-01-09
YU185579A (en)	1982-02-28
IL45165A0 (en)	1974-10-22
USB484419I5 (fr)	1976-03-09
IL45165A (en)	1977-06-30
YU185574A (en)	1982-02-28

Publication	Publication Date	Title
EP0007990B1 (fr)	1981-03-25	Pyrazol-éthers, leur procédé de préparation et herbicides les contenant
NO142800B (no)	1980-07-14	Herbicide preparater inneholdende pyrazolderivater
NZ236199A (en)	1994-03-25	5-benzyl-2-isoxazoline-3-carboxylic acid derivative, preparation and use as a plant protective agent
JPS59205368A (ja)	1984-11-20	殺微生物剤
JPS58103374A (ja)	1983-06-20	１，３，５−トリアジノン、その製造法及び該化合物を有効物質として含有する除草剤
DE2915250A1 (de)	1980-10-30	Salze von alpha -aminoacetaniliden
EP0071794A1 (fr)	1983-02-16	Dérivés de l'acide 5-amino-1-phényl-pyrazol-4-carboxylique, leur procédé de préparation et leur application comme herbicides
EP0003805A1 (fr)	1979-09-05	Pyridazones et compositions herbicides les contenant
EP0149034A2 (fr)	1985-07-24	Régulation du métabolisme des plantes avec des acides carboxyliques alpha,bêta ou bêta,gamma insaturés ou leurs dérivés
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
US4376645A (en)	1983-03-15	2'-Phenylhydrazino-2-cyanoacrylic acid esters and herbicides containing these compounds
NO742711L (fr)	1975-03-17
NO742407L (fr)	1975-02-03
EP0013873B1 (fr)	1982-01-20	Anilides de l'acide N-azolyl acétique, procédé pour leur préparation et leur utilisation comme herbicides
NO750266L (fr)	1975-08-25
NO742396L (fr)	1975-01-10
EP0007588B1 (fr)	1981-05-13	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
EP0107123B1 (fr)	1987-07-01	Dérivés d'aniline, procédé pour leur préparation et leur utilisation dans la lutte contre la croissance des plantes indésirables
DE3818848A1 (de)	1989-12-07	Pyridazinonderivate, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung im pflanzenschutz
NO750140L (fr)	1975-08-11
EP0067381B1 (fr)	1984-03-21	Anilides, procédé pour leur préparation et herbicides les contenant
EP0291809B1 (fr)	1992-01-15	Anilino-2 quinoléines, procédé pour leur préparation et fongicides les contenant
DE2210540A1 (de)	1973-09-06	Cyanphenylcarbonate
US4025544A (en)	1977-05-24	O-alkylsulfonylglycolic anilides
NO742869L (fr)	1975-03-17