DD242955A5 - Pflanzenschutzmittel - Google Patents

Pflanzenschutzmittel Download PDF

Info

Publication number: DD242955A5
Authority: DD; German Democratic Republic
Prior art keywords: weight; general formula; contain; carbon atoms; methyl
Prior art date: 1984-11-23

Application number

DD85283142A

Other languages

German (de)

English (en)

Inventor

Gyoergy Lanyi

Lajos Nagy

Valeria Denes

Eva Somfai

Erzsebet Radvany

Laszlo Pap

Maria Visnyovszky

Tamas Detre

Andras Szego

Original Assignee

��@��@��@��@��@��@��Kk��

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.)

1984-11-23

Filing date

1985-11-22

Publication date

1987-02-18

1985-11-22 Application filed by ��@��@��@��@��@��@��Kk�� filed Critical ��@��@��@��@��@��@��Kk��

1987-02-18 Publication of DD242955A5 publication Critical patent/DD242955A5/de

Links

239000000575 pesticide Substances 0.000 title 1
150000001875 compounds Chemical class 0.000 claims abstract description 31
150000003839 salts Chemical class 0.000 claims abstract description 19
238000000034 method Methods 0.000 claims abstract description 10
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 6
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
239000001257 hydrogen Substances 0.000 claims abstract description 6
238000002360 preparation method Methods 0.000 claims abstract description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 4
239000000203 mixture Substances 0.000 claims description 31
239000004480 active ingredient Substances 0.000 claims description 24
239000008187 granular material Substances 0.000 claims description 18
239000002904 solvent Substances 0.000 claims description 15
239000013543 active substance Substances 0.000 claims description 10
125000004432 carbon atom Chemical group C* 0.000 claims description 10
239000000839 emulsion Substances 0.000 claims description 10
239000012141 concentrate Substances 0.000 claims description 8
241000238631 Hexapoda Species 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 7
239000003795 chemical substances by application Substances 0.000 claims description 7
239000002736 nonionic surfactant Substances 0.000 claims description 7
239000000546 pharmaceutical excipient Substances 0.000 claims description 7
239000004094 surface-active agent Substances 0.000 claims description 7
125000000129 anionic group Chemical group 0.000 claims description 5
239000003945 anionic surfactant Substances 0.000 claims description 5
239000000969 carrier Substances 0.000 claims description 5
239000002689 soil Substances 0.000 claims description 5
239000000126 substance Substances 0.000 claims description 5
230000002195 synergetic effect Effects 0.000 claims description 5
239000000853 adhesive Substances 0.000 claims description 4
230000001070 adhesive effect Effects 0.000 claims description 4
239000003381 stabilizer Substances 0.000 claims description 4
239000004546 suspension concentrate Substances 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000004663 dialkyl amino group Chemical group 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims description 2
239000004476 plant protection product Substances 0.000 claims description 2
239000012747 synergistic agent Substances 0.000 claims 2
239000000975 dye Substances 0.000 claims 1
238000004945 emulsification Methods 0.000 claims 1
125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 63
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 36
239000000243 solution Substances 0.000 description 33
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 15
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
-1 Alkyl phenol Chemical compound 0.000 description 8
DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 description 8
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 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
238000000921 elemental analysis Methods 0.000 description 6
CICIUHBGFXYUHS-UHFFFAOYSA-N [chloro-(2,2-dimethyl-3H-1-benzofuran-7-yl)methyl]-methylcarbamic acid Chemical compound OC(=O)N(C)C(Cl)C1=CC=CC2=C1OC(C)(C)C2 CICIUHBGFXYUHS-UHFFFAOYSA-N 0.000 description 5
239000000654 additive Substances 0.000 description 5
239000002671 adjuvant Substances 0.000 description 5
230000000749 insecticidal effect Effects 0.000 description 5
238000003756 stirring Methods 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
229920003171 Poly (ethylene oxide) Polymers 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
241000607479 Yersinia pestis Species 0.000 description 4
238000013459 approach Methods 0.000 description 4
230000007935 neutral effect Effects 0.000 description 4
IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 4
239000000725 suspension Substances 0.000 description 4
WJGPNUBJBMCRQH-UHFFFAOYSA-N 2,2-dimethyl-2,3-dihydro-1-benzofuran-7-ol Chemical compound C1=CC(O)=C2OC(C)(C)CC2=C1 WJGPNUBJBMCRQH-UHFFFAOYSA-N 0.000 description 3
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
241000254173 Coleoptera Species 0.000 description 3
SDKQRNRRDYRQKY-UHFFFAOYSA-N Dioxacarb Chemical compound CNC(=O)OC1=CC=CC=C1C1OCCO1 SDKQRNRRDYRQKY-UHFFFAOYSA-N 0.000 description 3
241000196324 Embryophyta Species 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
241000257159 Musca domestica Species 0.000 description 3
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 3
241000700159 Rattus Species 0.000 description 3
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
230000000895 acaricidal effect Effects 0.000 description 3
125000002877 alkyl aryl group Chemical group 0.000 description 3
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 3
239000002585 base Substances 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
230000000694 effects Effects 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
239000012071 phase Substances 0.000 description 3
229910052938 sodium sulfate Inorganic materials 0.000 description 3
235000011152 sodium sulphate Nutrition 0.000 description 3
RHUYHJGZWVXEHW-UHFFFAOYSA-N 1,1-Dimethyhydrazine Chemical compound CN(C)N RHUYHJGZWVXEHW-UHFFFAOYSA-N 0.000 description 2
241000238876 Acari Species 0.000 description 2
241001124076 Aphididae Species 0.000 description 2
241001388466 Bruchus rufimanus Species 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
241000255925 Diptera Species 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
241000257226 Muscidae Species 0.000 description 2
241000244206 Nematoda Species 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
229930040373 Paraformaldehyde Natural products 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
240000006677 Vicia faba Species 0.000 description 2
150000001447 alkali salts Chemical class 0.000 description 2
239000000645 desinfectant Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
238000009472 formulation Methods 0.000 description 2
ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical group C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 2
239000011521 glass Substances 0.000 description 2
239000002563 ionic surfactant Substances 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
235000012054 meals Nutrition 0.000 description 2
NULJZZQMTQVLPG-UHFFFAOYSA-N n,n-dimethylmorpholin-4-amine Chemical compound CN(C)N1CCOCC1 NULJZZQMTQVLPG-UHFFFAOYSA-N 0.000 description 2
CDEGPTONQNEAIP-UHFFFAOYSA-N n-methyl-1-morpholin-4-ylmethanamine Chemical compound CNCN1CCOCC1 CDEGPTONQNEAIP-UHFFFAOYSA-N 0.000 description 2
VLNZTVFATQZKQP-UHFFFAOYSA-N n-methyl-n-(morpholin-4-ylmethyl)carbamoyl chloride Chemical compound ClC(=O)N(C)CN1CCOCC1 VLNZTVFATQZKQP-UHFFFAOYSA-N 0.000 description 2
239000005645 nematicide Substances 0.000 description 2
239000003921 oil Substances 0.000 description 2
235000019198 oils Nutrition 0.000 description 2
239000012074 organic phase Substances 0.000 description 2
229920002866 paraformaldehyde Polymers 0.000 description 2
239000002245 particle Substances 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
235000012424 soybean oil Nutrition 0.000 description 2
239000003549 soybean oil Substances 0.000 description 2
239000007858 starting material Substances 0.000 description 2
235000000346 sugar Nutrition 0.000 description 2
230000009885 systemic effect Effects 0.000 description 2
150000003512 tertiary amines Chemical class 0.000 description 2
238000012360 testing method Methods 0.000 description 2
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
231100000419 toxicity Toxicity 0.000 description 2
230000001988 toxicity Effects 0.000 description 2
239000008096 xylene Substances 0.000 description 2
MQTMIQSZMVPFQB-UHFFFAOYSA-N (2,2-dimethyl-3H-1-benzofuran-7-yl)-methylcarbamic acid Chemical compound OC(=O)N(C)C1=CC=CC2=C1OC(C)(C)C2 MQTMIQSZMVPFQB-UHFFFAOYSA-N 0.000 description 1
LFIQOFYSVSBJNH-UHFFFAOYSA-N (2,2-dimethyl-3h-1-benzofuran-7-yl) carbonochloridate Chemical compound C1=CC(OC(Cl)=O)=C2OC(C)(C)CC2=C1 LFIQOFYSVSBJNH-UHFFFAOYSA-N 0.000 description 1
OVANCIHPSBMNEN-UHFFFAOYSA-N (2,2-dimethyl-3h-1-benzofuran-7-yl)methylcarbamic acid Chemical compound C1=CC(CNC(O)=O)=C2OC(C)(C)CC2=C1 OVANCIHPSBMNEN-UHFFFAOYSA-N 0.000 description 1
YHAROSAFXOQKCZ-UHFFFAOYSA-N 1-benzofuran-2-ol Chemical compound C1=CC=C2OC(O)=CC2=C1 YHAROSAFXOQKCZ-UHFFFAOYSA-N 0.000 description 1
QQGRFMIMXPWKPM-UHFFFAOYSA-N 2,3,4-tributylphenol Chemical compound CCCCC1=CC=C(O)C(CCCC)=C1CCCC QQGRFMIMXPWKPM-UHFFFAOYSA-N 0.000 description 1
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
ANOUKFYBOAKOIR-UHFFFAOYSA-N 3,4-dimethoxyphenylethylamine Chemical compound COC1=CC=C(CCN)C=C1OC ANOUKFYBOAKOIR-UHFFFAOYSA-N 0.000 description 1
229910002012 Aerosil® Inorganic materials 0.000 description 1
206010002091 Anaesthesia Diseases 0.000 description 1
241000605281 Anaplasma phagocytophilum Species 0.000 description 1
241000239290 Araneae Species 0.000 description 1
240000007124 Brassica oleracea Species 0.000 description 1
235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical group ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
206010020591 Hypercapnia Diseases 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
241000131102 Oryzaephilus Species 0.000 description 1
206010033799 Paralysis Diseases 0.000 description 1
241000254112 Tribolium confusum Species 0.000 description 1
235000010749 Vicia faba Nutrition 0.000 description 1
235000002096 Vicia faba var. equina Nutrition 0.000 description 1
CWGPVAJMHGQVST-UHFFFAOYSA-N [(2,2-dimethyl-3H-1-benzofuran-7-yl)-(propan-2-ylamino)methyl]-methylcarbamic acid Chemical compound CC(C)NC(C1=CC=CC2=C1OC(C2)(C)C)N(C)C(=O)O CWGPVAJMHGQVST-UHFFFAOYSA-N 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
230000001154 acute effect Effects 0.000 description 1
230000007059 acute toxicity Effects 0.000 description 1
231100000403 acute toxicity Toxicity 0.000 description 1
239000002154 agricultural waste Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000005215 alkyl ethers Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
HHFJXGNFTBSDLF-UHFFFAOYSA-N aminomethylcarbamic acid Chemical compound NCNC(O)=O HHFJXGNFTBSDLF-UHFFFAOYSA-N 0.000 description 1
230000037005 anaesthesia Effects 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
230000002528 anti-freeze Effects 0.000 description 1
239000000010 aprotic solvent Substances 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
239000011324 bead Substances 0.000 description 1
ISGXZRIDYZBDFG-UHFFFAOYSA-N butan-1-ol;butan-2-one Chemical compound CCCCO.CCC(C)=O ISGXZRIDYZBDFG-UHFFFAOYSA-N 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
235000013877 carbamide Nutrition 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
239000003086 colorant Substances 0.000 description 1
229940125904 compound 1 Drugs 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000007865 diluting Methods 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
125000001891 dimethoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
125000003700 epoxy group Chemical group 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000006260 foam Substances 0.000 description 1
238000005187 foaming Methods 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
238000000227 grinding Methods 0.000 description 1
231100000086 high toxicity Toxicity 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
239000008101 lactose Substances 0.000 description 1
230000001418 larval effect Effects 0.000 description 1
238000005339 levitation Methods 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000001064 morpholinomethyl group Chemical group [H]C([H])(*)N1C([H])([H])C([H])([H])OC([H])([H])C1([H])[H] 0.000 description 1
230000001069 nematicidal effect Effects 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
229920001522 polyglycol ester Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
235000019422 polyvinyl alcohol Nutrition 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000011435 rock Substances 0.000 description 1
239000004576 sand Substances 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
238000000926 separation method Methods 0.000 description 1
238000007873 sieving Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
150000008163 sugars Chemical class 0.000 description 1
125000005270 trialkylamine group Chemical group 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/86—Benzo [b] furans; Hydrogenated benzo [b] furans with an oxygen atom directly attached in position 7

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Furan Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD85283142A 1984-11-23 1985-11-22 Pflanzenschutzmittel DD242955A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
HU844346A HU193062B (en)	1984-11-23	1984-11-23	Insecticide compositions containing o-benzofuranyl-carbamate derivatives as active substances and process for preparing o-benzofuranyl-carbamate derivatives

Publications (1)

Publication Number	Publication Date
DD242955A5 true DD242955A5 (de)	1987-02-18

Family

ID=10967715

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD85283142A DD242955A5 (de)	1984-11-23	1985-11-22	Pflanzenschutzmittel

Country Status (17)

Country	Link
US (1)	US4788217A (cs)
EP (1)	EP0203954B1 (cs)
JP (1)	JPH0655735B2 (cs)
KR (1)	KR870700617A (cs)
CN (1)	CN1007953B (cs)
AT (1)	ATE46154T1 (cs)
BR (1)	BR8507069A (cs)
CS (1)	CS253733B2 (cs)
DD (1)	DD242955A5 (cs)
DE (1)	DE3572811D1 (cs)
ES (3)	ES8704159A1 (cs)
HU (1)	HU193062B (cs)
IE (1)	IE58469B1 (cs)
IL (1)	IL77121A (cs)
PL (1)	PL151228B1 (cs)
SU (1)	SU1450745A3 (cs)
WO (1)	WO1986003202A1 (cs)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0372406A (ja) *	1989-05-10	1991-03-27	Hodogaya Chem Co Ltd	チオールカーバメイト粒剤
US5283066A (en) *	1992-02-19	1994-02-01	Development Center For Biotechnology	Method of stimulating an immune response by using a hapten

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL6917884A (en) *	1969-11-28	1971-06-02		N-alkyl carbamate insecticides
US3929838A (en) *	1972-05-27	1975-12-30	Bayer Ag	N-methyl-n-(3-trifluoromethylphenylmercapto)-carbamic acid dihydrobenzofuranyl esters
TR20962A (tr) *	1981-06-02	1983-02-25	Otsuka Chemical Co Ltd	Karbamat tuerevleri,bunlari ihtive eden ensektisid,midisid veya nematosid bilesimler ve bunlari hazirlamaya mahsus usul

1984
- 1984-11-23 HU HU844346A patent/HU193062B/hu not_active IP Right Cessation
1985
- 1985-11-15 WO PCT/HU1985/000068 patent/WO1986003202A1/en not_active Ceased
- 1985-11-15 EP EP85905871A patent/EP0203954B1/en not_active Expired
- 1985-11-15 DE DE8585905871T patent/DE3572811D1/de not_active Expired
- 1985-11-15 AT AT85905871T patent/ATE46154T1/de not_active IP Right Cessation
- 1985-11-15 BR BR8507069A patent/BR8507069A/pt not_active IP Right Cessation
- 1985-11-15 US US06/901,448 patent/US4788217A/en not_active Expired - Fee Related
- 1985-11-15 JP JP60505208A patent/JPH0655735B2/ja not_active Expired - Lifetime
- 1985-11-21 IE IE293085A patent/IE58469B1/en not_active IP Right Cessation
- 1985-11-22 CN CN85109349A patent/CN1007953B/zh not_active Expired
- 1985-11-22 CS CS858445A patent/CS253733B2/cs unknown
- 1985-11-22 IL IL77121A patent/IL77121A/xx not_active IP Right Cessation
- 1985-11-22 DD DD85283142A patent/DD242955A5/de not_active IP Right Cessation
- 1985-11-22 ES ES549802A patent/ES8704159A1/es not_active Expired
- 1985-11-22 PL PL1985256400A patent/PL151228B1/pl unknown
1986
- 1986-07-21 SU SU864027826A patent/SU1450745A3/ru active
- 1986-07-23 KR KR860700490A patent/KR870700617A/ko not_active Withdrawn
- 1986-12-16 ES ES557283A patent/ES8708133A1/es not_active Expired
- 1986-12-16 ES ES557284A patent/ES8801911A1/es not_active Expired

Also Published As

Publication number	Publication date
DE3572811D1 (en)	1989-10-12
ATE46154T1 (de)	1989-09-15
PL256400A1 (en)	1988-01-21
CN1007953B (zh)	1990-05-16
JPS62501209A (ja)	1987-05-14
KR870700617A (ko)	1987-12-30
ES8704159A1 (es)	1987-04-01
IL77121A (en)	1991-01-31
EP0203954B1 (en)	1989-09-06
HU193062B (en)	1987-08-28
EP0203954A1 (en)	1986-12-10
ES8708133A1 (es)	1987-10-16
PL151228B1 (en)	1990-08-31
SU1450745A3 (ru)	1989-01-07
CN85109349A (zh)	1986-10-29
IL77121A0 (en)	1986-04-29
BR8507069A (pt)	1987-07-14
CS253733B2 (en)	1987-12-17
ES549802A0 (es)	1987-04-01
ES557284A0 (es)	1988-03-16
IE58469B1 (en)	1993-09-22
IE852930L (en)	1986-05-23
WO1986003202A1 (en)	1986-06-05
HUT38209A (en)	1986-05-28
ES8801911A1 (es)	1988-03-16
JPH0655735B2 (ja)	1994-07-27
ES557283A0 (es)	1987-10-16
US4788217A (en)	1988-11-29

Legal Events

Date	Code	Title	Description
2002-09-26	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
EP0210487B1 (de)	1989-12-13	Verwendung von N-(4-Phenoxy-2,6-diisopropylphenyl)-N'-tert.butylthioharnstoff zur Bekämpfung von weissen Fliegen
DE69028461T2 (de)	1997-02-06	Triazin-derivate und unkrautvertilgungsmittel daraus
EP0303570A2 (de)	1989-02-15	Substituierte Isothioharnstoffe
DE2433680B2 (de)	1979-05-17	23-DUiydro-2^-dimethyl-7-benzofuranyl-methyl-carbamat-N-aminosulfenylderivate, Verfahren zu deren Herstellung und diese Verbindungen enthaltende insektizide Zubereitungen
DE2654314C2 (cs)	1987-06-25
DE2328374A1 (de)	1973-12-20	Insektizide mittel
EP0191734B1 (de)	1990-01-10	Schädlingsbekämpfungsmittel
DE2619303A1 (de)	1976-11-18	Neue schwefelhaltige bisformamidine, verfahren zu ihrer herstellung und verwendung derselben sowie diese enthaltende land-, garten- und forstwirtschaftliche chemikalien
DE1643143A1 (de)	1971-01-21	Pestizide und Verfahren zu deren Herstellung
DD242955A5 (de)	1987-02-18	Pflanzenschutzmittel
DE2147850A1 (de)	1972-06-08	Carbamidsäurederivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Pestizide
EP0113317B1 (de)	1989-08-02	Carbamate
DD262992A5 (de)	1988-12-21	Nematizide und insektizide zusammensetzung
DD209444A5 (de)	1984-05-09	Verfahren zur herstellung von carbamatderivaten
EP0390740A1 (de)	1990-10-03	Schädlingsbekämpfung
DE2260763C3 (de)	1979-11-29	Bekämpfung von schädlichen Organismen mit Dihalogenpropansulfonsäureesterderivaten
DE3134596A1 (de)	1982-08-19	Carbamatderivate, insektizide, antimilben- oder nematozide zusammensetzungen, welche diese enthalten, und verfahren zu deren herstellung
EP0390741A1 (de)	1990-10-03	Schädlingsbekämpfung
DE2018419A1 (cs)	1970-11-12
DD236868A5 (de)	1986-06-25	Mittel zum protahieren der wirkungsdauer und zur erhoehung der selektivitaet von herbiziden zusammensetzungen
AT362197B (de)	1981-04-27	Verfahren zur bekaempfung von insekten, milben und nematoden
EP0094909B1 (de)	1986-11-05	N-Alkyliden-imino-oxicarbonyl-N-methyl-(2,2-dimethyl-2,3-di-hydrobenzofuranyl(7))-carbamate, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung
EP0053096A1 (de)	1982-06-02	Unsymmetrische Bis-Carbamate, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung
EP0051565A1 (de)	1982-05-12	1-N,N-Dimethylcarbamoyl-3(5)-cyclopropyl-1,2,4-triazole, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung
DE1568060C3 (de)	1973-12-06	4,4' Dibrom benzilsäure isopropyl ester, Verfahren zu seiner Herstellung und Verwendung dieses Esters zur Be kampfung von Spinnentieren und Insekten