PL72582B1 - - Google Patents

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Publication number: PL72582B1
Authority: PL; Poland
Prior art keywords: phenyl; carbamic acid; ester; carbamoyloxy; carbamic
Prior art date: 1967-09-20

Application number

PL1968129135A

Other languages

English (en)

Polish (pl)

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.)

1967-09-20

Filing date

1968-09-19

Publication date

1974-08-30

1968-09-19 Application filed filed Critical

1974-08-30 Publication of PL72582B1 publication Critical patent/PL72582B1/pl

Links

-1 for example Substances 0.000 claims description 33
239000000203 mixture Substances 0.000 claims description 22
239000004009 herbicide Substances 0.000 claims description 9
150000001875 compounds Chemical class 0.000 claims description 8
230000002363 herbicidal effect Effects 0.000 claims description 8
239000000969 carrier Substances 0.000 claims description 5
229910052757 nitrogen Inorganic materials 0.000 claims description 5
239000007788 liquid Substances 0.000 claims description 4
238000000034 method Methods 0.000 claims description 4
125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
239000004480 active ingredient Substances 0.000 claims description 3
125000004414 alkyl thio group Chemical group 0.000 claims description 3
125000001188 haloalkyl group Chemical group 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
239000007787 solid Substances 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
239000000654 additive Substances 0.000 claims description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
125000003710 aryl alkyl group Chemical group 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
125000000623 heterocyclic group Chemical group 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000002904 solvent Substances 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
125000001931 aliphatic group Chemical group 0.000 claims 1
125000003277 amino group Chemical group 0.000 claims 1
150000003857 carboxamides Chemical class 0.000 claims 1
125000004966 cyanoalkyl group Chemical group 0.000 claims 1
125000004430 oxygen atom Chemical group O* 0.000 claims 1
239000002253 acid Substances 0.000 description 30
241000196324 Embryophyta Species 0.000 description 12
125000004093 cyano group Chemical group *C#N 0.000 description 12
150000004702 methyl esters Chemical class 0.000 description 8
239000003795 chemical substances by application Substances 0.000 description 7
239000013543 active substance Substances 0.000 description 6
KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 6
150000002148 esters Chemical class 0.000 description 6
239000004615 ingredient Substances 0.000 description 5
KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 5
125000004494 ethyl ester group Chemical group 0.000 description 4
150000003254 radicals Chemical class 0.000 description 4
235000021537 Beetroot Nutrition 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
125000001309 chloro group Chemical group Cl* 0.000 description 3
230000000694 effects Effects 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000003921 oil Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
230000004071 biological effect Effects 0.000 description 2
229940088623 biologically active substance Drugs 0.000 description 2
150000004657 carbamic acid derivatives Chemical class 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
230000001066 destructive effect Effects 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
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
NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical class CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
241000208479 Anagallis arvensis Species 0.000 description 1
241000681416 Anchusa arvensis Species 0.000 description 1
235000009066 Atriplex patula Nutrition 0.000 description 1
244000022181 Atriplex patula Species 0.000 description 1
235000005781 Avena Nutrition 0.000 description 1
244000075850 Avena orientalis Species 0.000 description 1
235000016068 Berberis vulgaris Nutrition 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
235000006463 Brassica alba Nutrition 0.000 description 1
235000008427 Brassica arvensis Nutrition 0.000 description 1
244000140786 Brassica hirta Species 0.000 description 1
244000024671 Brassica kaber Species 0.000 description 1
235000004977 Brassica sinapistrum Nutrition 0.000 description 1
235000011305 Capsella bursa pastoris Nutrition 0.000 description 1
240000008867 Capsella bursa-pastoris Species 0.000 description 1
235000005940 Centaurea cyanus Nutrition 0.000 description 1
240000004385 Centaurea cyanus Species 0.000 description 1
240000006122 Chenopodium album Species 0.000 description 1
235000009344 Chenopodium album Nutrition 0.000 description 1
244000192528 Chrysanthemum parthenium Species 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
244000192024 Euphorbia helioscopia Species 0.000 description 1
235000012043 Euphorbia helioscopia Nutrition 0.000 description 1
241001289540 Fallopia convolvulus Species 0.000 description 1
240000009088 Fragaria x ananassa Species 0.000 description 1
244000044980 Fumaria officinalis Species 0.000 description 1
235000006961 Fumaria officinalis Nutrition 0.000 description 1
241000520028 Lamium Species 0.000 description 1
235000017945 Matricaria Nutrition 0.000 description 1
235000007232 Matricaria chamomilla Nutrition 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000209117 Panicum Species 0.000 description 1
235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 1
235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 1
235000007846 Papaver rhoeas Nutrition 0.000 description 1
240000004674 Papaver rhoeas Species 0.000 description 1
241000881225 Persicaria Species 0.000 description 1
240000006928 Persicaria lapathifolia Species 0.000 description 1
CXOFVDLJLONNDW-UHFFFAOYSA-N Phenytoin Chemical group N1C(=O)NC(=O)C1(C=1C=CC=CC=1)C1=CC=CC=C1 CXOFVDLJLONNDW-UHFFFAOYSA-N 0.000 description 1
241000209504 Poaceae Species 0.000 description 1
235000006386 Polygonum aviculare Nutrition 0.000 description 1
244000292697 Polygonum aviculare Species 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
241000218206 Ranunculus Species 0.000 description 1
244000286177 Raphanus raphanistrum Species 0.000 description 1
235000000241 Raphanus raphanistrum Nutrition 0.000 description 1
240000003705 Senecio vulgaris Species 0.000 description 1
235000002594 Solanum nigrum Nutrition 0.000 description 1
244000061457 Solanum nigrum Species 0.000 description 1
244000113423 Sonchus asper Species 0.000 description 1
235000006744 Sonchus asper Nutrition 0.000 description 1
241000960310 Spergula Species 0.000 description 1
235000009337 Spinacia oleracea Nutrition 0.000 description 1
244000300264 Spinacia oleracea Species 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
240000006694 Stellaria media Species 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
235000008214 Thlaspi arvense Nutrition 0.000 description 1
240000008488 Thlaspi arvense Species 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
235000009108 Urtica dioica Nutrition 0.000 description 1
240000001261 Urtica urens Species 0.000 description 1
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
GRTOGORTSDXSFK-XJTZBENFSA-N ajmalicine Chemical compound C1=CC=C2C(CCN3C[C@@H]4[C@H](C)OC=C([C@H]4C[C@H]33)C(=O)OC)=C3NC2=C1 GRTOGORTSDXSFK-XJTZBENFSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
125000004799 bromophenyl group Chemical group 0.000 description 1
PVEOYINWKBTPIZ-UHFFFAOYSA-N but-3-enoic acid Chemical compound OC(=O)CC=C PVEOYINWKBTPIZ-UHFFFAOYSA-N 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
125000004432 carbon atom Chemical group C* 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
230000006378 damage Effects 0.000 description 1
230000000254 damaging effect Effects 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
LFMVFTMUPCOARK-UHFFFAOYSA-N ethane-1,2-diol;oxirane Polymers C1CO1.OCCO LFMVFTMUPCOARK-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers 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
239000008187 granular material Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000002367 halogens Chemical class 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
ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 description 1
239000004571 lime Substances 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000002480 mineral oil Substances 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
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
239000000243 solution Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000010959 steel Substances 0.000 description 1
235000021012 strawberries Nutrition 0.000 description 1
150000003462 sulfoxides Chemical class 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
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
239000012749 thinning agent Substances 0.000 description 1
150000003672 ureas Chemical group 0.000 description 1
235000012431 wafers Nutrition 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

PL1968129135A 1967-09-20 1968-09-19 PL72582B1 (cs)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE1642346		1967-09-20

Publications (1)

Publication Number	Publication Date
PL72582B1 true PL72582B1 (cs)	1974-08-30

Family

ID=5684180

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PL1968129135A PL72582B1 (cs)	1967-09-20	1968-09-19

Country Status (5)

Country	Link
CH (1)	CH505540A (cs)
CS (1)	CS157645B2 (cs)
ES (1)	ES357597A1 (cs)
IE (1)	IE32330B1 (cs)
PL (1)	PL72582B1 (cs)

1968
- 1968-07-29 CH CH1134068A patent/CH505540A/de not_active IP Right Cessation
- 1968-08-23 CS CS606068A patent/CS157645B2/cs unknown
- 1968-08-27 ES ES357597A patent/ES357597A1/es not_active Expired
- 1968-09-11 IE IE1098/68A patent/IE32330B1/xx unknown
- 1968-09-19 PL PL1968129135A patent/PL72582B1/pl unknown

Also Published As

Publication number	Publication date
IE32330L (en)	1969-03-20
ES357597A1 (es)	1970-03-16
CH505540A (de)	1971-04-15
CS157645B2 (cs)	1974-09-16
IE32330B1 (en)	1973-06-27

Publication	Publication Date	Title
US4424363A (en)	1984-01-03	Substituted 3-aminopyrazoles
EP2213170B1 (de)	2012-09-19	Herbizide Mittel auf Basis von Heteroaryloxyacetamiden
CA1157022A (en)	1983-11-15	Substituted ureas, their manufacture, their use as herbicides, and agents therefor
EP0094541A2 (de)	1983-11-23	Substituierte 5-Trifluormethyl-1,3,4-thiadiazol-2-yl-oxyessigsäureamide, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide
EP0363585A1 (de)	1990-04-18	N-Aryl-Stickstoffheterocyclen
DD149992A5 (de)	1981-08-12	Herbizide mittel
US4500340A (en)	1985-02-19	Urea derivatives and their use for controlling undesirable plant growth
PL72582B1 (cs)	1974-08-30
US4426222A (en)	1984-01-17	Carbaminic acid esters with herbicidal properties
CA1152994A (en)	1983-08-30	Cyanoalkyl-phenylureas having selective herbicidal activity, their production, and compositions containing them
DE3431917A1 (de)	1986-03-13	1-(2-trifluormethoxy-phenylsulfonyl)-3- heteroaryl-(thio)-harnstoffe
CS247172B2 (en)	1986-12-18	Fungicide and method of active substance preparation
EP0171544A1 (de)	1986-02-19	Substituierte 5-Acylamino-1-phenylpyrazole
DE3038635C2 (cs)	1989-02-16
US4844729A (en)	1989-07-04	Substituted N-phenylpyridazone derivatives
US4283547A (en)	1981-08-11	Parabanic acid derivatives
US4131751A (en)	1978-12-26	Diurethanes
EP0159576A2 (de)	1985-10-30	2-(Alkoximinoalkyloxycarbonyl)-phenylsulfonylharnstoffe
HU185779B (en)	1985-03-28	Herbicides containing carbamic acid phenyl esters
EP0164017A2 (de)	1985-12-11	Substituierte Phenylsulfonylharnstoffe
CA1139777A (en)	1983-01-18	N-sulfenylated diurethanes
DE1809838C3 (de)	1978-01-05	N-(3-Brom-4-chlorphenyl)-N'methoxy-N'-methylharnstoff und seine Verwendung als Herbizid
DE4018352A1 (de)	1991-12-12	Cycloalkyl-substituierte thiadiazolyloxyessigsaeureamide
IE46905B1 (en)	1983-11-02	Sulfurous diurethanes
DE3541260A1 (de)	1987-05-27	N-(4-tert.-butoxy-phenyl)-harnstoffe