CN1064388A - 用于促进和抑制植物生长的制剂 - Google Patents
用于促进和抑制植物生长的制剂 Download PDFInfo
- Publication number
- CN1064388A CN1064388A CN91102096.9A CN91102096A CN1064388A CN 1064388 A CN1064388 A CN 1064388A CN 91102096 A CN91102096 A CN 91102096A CN 1064388 A CN1064388 A CN 1064388A
- Authority
- CN
- China
- Prior art keywords
- urea
- compound
- preparation
- active principle
- sulfonyl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
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- 238000002360 preparation method Methods 0.000 title claims abstract description 28
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 6
- 229910052700 potassium Inorganic materials 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims abstract description 5
- 239000004202 carbamide Substances 0.000 claims description 32
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 31
- -1 triazinyl urea Chemical compound 0.000 claims description 20
- 150000003839 salts Chemical class 0.000 claims description 7
- 159000000000 sodium salts Chemical class 0.000 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 5
- 239000011591 potassium Substances 0.000 claims description 5
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 12
- FENAOFFCBUFUEY-UHFFFAOYSA-N 1-(benzenesulfonyl)-1-(triazin-4-yl)urea Chemical compound C=1C=CC=CC=1S(=O)(=O)N(C(=O)N)C1=CC=NN=N1 FENAOFFCBUFUEY-UHFFFAOYSA-N 0.000 abstract description 11
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 2
- 229910052708 sodium Inorganic materials 0.000 abstract description 2
- 150000002148 esters Chemical class 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 description 35
- 241000196324 Embryophyta Species 0.000 description 33
- 230000012010 growth Effects 0.000 description 20
- 239000002689 soil Substances 0.000 description 20
- 240000008042 Zea mays Species 0.000 description 18
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 18
- 230000000694 effects Effects 0.000 description 18
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 17
- 239000000460 chlorine Substances 0.000 description 17
- 235000005822 corn Nutrition 0.000 description 17
- 238000012360 testing method Methods 0.000 description 11
- 238000003306 harvesting Methods 0.000 description 10
- IWZSHWBGHQBIML-ZGGLMWTQSA-N (3S,8S,10R,13S,14S,17S)-17-isoquinolin-7-yl-N,N,10,13-tetramethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-amine Chemical compound CN(C)[C@H]1CC[C@]2(C)C3CC[C@@]4(C)[C@@H](CC[C@@H]4c4ccc5ccncc5c4)[C@@H]3CC=C2C1 IWZSHWBGHQBIML-ZGGLMWTQSA-N 0.000 description 9
- 238000001228 spectrum Methods 0.000 description 9
- 240000008067 Cucumis sativus Species 0.000 description 8
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 8
- 238000000034 method Methods 0.000 description 7
- OSFBJERFMQCEQY-UHFFFAOYSA-N propylidene Chemical group [CH]CC OSFBJERFMQCEQY-UHFFFAOYSA-N 0.000 description 7
- 229930191978 Gibberellin Natural products 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- LNUFLCYMSVYYNW-ZPJMAFJPSA-N [(2r,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[[(3s,5s,8r,9s,10s,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-disulfo Chemical compound O([C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1C[C@@H]2CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)[C@H]1O[C@H](COS(O)(=O)=O)[C@@H](OS(O)(=O)=O)[C@H](OS(O)(=O)=O)[C@H]1OS(O)(=O)=O LNUFLCYMSVYYNW-ZPJMAFJPSA-N 0.000 description 6
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 6
- 229940125904 compound 1 Drugs 0.000 description 6
- IXORZMNAPKEEDV-UHFFFAOYSA-N gibberellic acid GA3 Natural products OC(=O)C1C2(C3)CC(=C)C3(O)CCC2C2(C=CC3O)C1C3(C)C(=O)O2 IXORZMNAPKEEDV-UHFFFAOYSA-N 0.000 description 6
- 239000003448 gibberellin Substances 0.000 description 6
- 238000002329 infrared spectrum Methods 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 5
- 239000002028 Biomass Substances 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 4
- 240000005979 Hordeum vulgare Species 0.000 description 4
- 235000007340 Hordeum vulgare Nutrition 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 241000209140 Triticum Species 0.000 description 4
- 235000021307 Triticum Nutrition 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- 210000000056 organ Anatomy 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- CSCPPACGZOOCGX-MICDWDOJSA-N 1-deuteriopropan-2-one Chemical compound [2H]CC(C)=O CSCPPACGZOOCGX-MICDWDOJSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 244000299507 Gossypium hirsutum Species 0.000 description 3
- 229940125782 compound 2 Drugs 0.000 description 3
- AEDZKIACDBYJLQ-UHFFFAOYSA-N ethane-1,2-diol;hydrate Chemical compound O.OCCO AEDZKIACDBYJLQ-UHFFFAOYSA-N 0.000 description 3
- 230000035784 germination Effects 0.000 description 3
- 238000009331 sowing Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- KCZIUKYAJJEIQG-UHFFFAOYSA-N 1,3,5-triazin-2-amine Chemical class NC1=NC=NC=N1 KCZIUKYAJJEIQG-UHFFFAOYSA-N 0.000 description 2
- 235000011305 Capsella bursa pastoris Nutrition 0.000 description 2
- 240000008867 Capsella bursa-pastoris Species 0.000 description 2
- 240000006122 Chenopodium album Species 0.000 description 2
- 235000009344 Chenopodium album Nutrition 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical class CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical class OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 241001289540 Fallopia convolvulus Species 0.000 description 2
- CJKRXEBLWJVYJD-UHFFFAOYSA-N N,N'-diethylethylenediamine Chemical compound CCNCCNCC CJKRXEBLWJVYJD-UHFFFAOYSA-N 0.000 description 2
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 2
- 241000018646 Pinus brutia Species 0.000 description 2
- 235000011613 Pinus brutia Nutrition 0.000 description 2
- 240000003461 Setaria viridis Species 0.000 description 2
- 235000002248 Setaria viridis Nutrition 0.000 description 2
- 235000010086 Setaria viridis var. viridis Nutrition 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000002178 crystalline material Substances 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 239000007952 growth promoter Substances 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- 239000004009 herbicide Substances 0.000 description 2
- 239000003864 humus Substances 0.000 description 2
- 230000008635 plant growth Effects 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 230000007115 recruitment Effects 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- JXCRRXJZIVGLRP-UHFFFAOYSA-N 4-(benzenesulfonyl)triazine urea Chemical compound NC(=O)N.C1(=CC=CC=C1)S(=O)(=O)C1=NN=NC=C1 JXCRRXJZIVGLRP-UHFFFAOYSA-N 0.000 description 1
- 235000007319 Avena orientalis Nutrition 0.000 description 1
- 241000209763 Avena sativa Species 0.000 description 1
- 235000007558 Avena sp Nutrition 0.000 description 1
- 208000003643 Callosities Diseases 0.000 description 1
- 241001148495 Cibotium barometz Species 0.000 description 1
- DPOBMEBPSQGSMB-UHFFFAOYSA-N ClC1=NC(=NC(=N1)C(C)C)N(CC)N Chemical class ClC1=NC(=NC(=N1)C(C)C)N(CC)N DPOBMEBPSQGSMB-UHFFFAOYSA-N 0.000 description 1
- 240000003173 Drymaria cordata Species 0.000 description 1
- 244000058871 Echinochloa crus-galli Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 206010020649 Hyperkeratosis 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
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 244000063486 Matricaria inodora Species 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 241001668545 Pascopyrum Species 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 240000000275 Persicaria hydropiper Species 0.000 description 1
- 235000017337 Persicaria hydropiper Nutrition 0.000 description 1
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 1
- 241000209056 Secale Species 0.000 description 1
- 235000007238 Secale cereale Nutrition 0.000 description 1
- 244000113428 Sonchus oleraceus Species 0.000 description 1
- 235000006745 Sonchus oleraceus Nutrition 0.000 description 1
- 229940100389 Sulfonylurea Drugs 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
- 241000404538 Tripleurospermum maritimum subsp. inodorum Species 0.000 description 1
- 241001464837 Viridiplantae Species 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- LJHFUFVRZNYVMK-ZDUSSCGKSA-N [3-[4-(aminomethyl)-6-(trifluoromethyl)pyridin-2-yl]oxyphenyl]-[(3S)-3-hydroxypyrrolidin-1-yl]methanone Chemical compound NCC1=CC(=NC(=C1)C(F)(F)F)OC=1C=C(C=CC=1)C(=O)N1C[C@H](CC1)O LJHFUFVRZNYVMK-ZDUSSCGKSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001408 amides Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000004380 ashing Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- WRJWRGBVPUUDLA-UHFFFAOYSA-N chlorosulfonyl isocyanate Chemical class ClS(=O)(=O)N=C=O WRJWRGBVPUUDLA-UHFFFAOYSA-N 0.000 description 1
- OMFXVFTZEKFJBZ-HJTSIMOOSA-N corticosterone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@H](CC4)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 OMFXVFTZEKFJBZ-HJTSIMOOSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 206010015037 epilepsy Diseases 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003324 growth hormone secretagogue Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Chemical class OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 230000003387 muscular Effects 0.000 description 1
- UJYAZVSPFMJCLW-UHFFFAOYSA-N n-(oxomethylidene)benzenesulfonamide Chemical class O=C=NS(=O)(=O)C1=CC=CC=C1 UJYAZVSPFMJCLW-UHFFFAOYSA-N 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003415 peat 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
- 230000008092 positive effect Effects 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000700 radioactive tracer Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 230000021217 seedling development Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- AWLUSOLTCFEHNE-UHFFFAOYSA-N sodium;urea Chemical compound [Na].NC(N)=O AWLUSOLTCFEHNE-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000012224 working solution Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D521/00—Heterocyclic compounds containing unspecified hetero rings
-
- 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU68891/91A AU631474B2 (en) | 1990-03-07 | 1990-03-07 | Substituted penylsulphonyltriazinylurea and salts thereof and means for stimulating and suppressing plant growth based on them |
| JP3500742A JPH05501415A (ja) | 1990-03-07 | 1990-03-07 | 置換フェニルスルホニルトリアジニル尿素、その塩並びにそれに基づく植物成長促進及び阻害用薬剤 |
| PCT/SU1990/000067 WO1991013880A1 (en) | 1990-03-07 | 1990-03-07 | Substituted penylsulphonyltriazinylurea and salts thereof and means for stimulating and suppressing plant growth based on them |
| DE4092524A DE4092524C2 (de) | 1990-03-07 | 1990-03-07 | Substituierte Phenylsulfonyltriazinylharnstoffe, deren Salze und Mittel mit pflanzenwachstumsregelierender Wirkung |
| DE19904092524 DE4092524T (enrdf_load_stackoverflow) | 1990-03-07 | 1990-03-07 | |
| CH3286/91A CH683341A5 (de) | 1990-03-07 | 1990-03-07 | Substituierte Phenylsulfonyltriazinylharnstoffe, deren Salze und Mittel zur Stimulation und Unterdrückung des Pflanzenwachstums auf deren Grundlage. |
| CA002036334A CA2036334C (en) | 1990-03-07 | 1991-02-14 | Substituted phenylsulphonyltriazinylureas, salts thereof and agent for plant growth stimulation and inhibition based thereon |
| CS91442A CS44291A3 (en) | 1990-03-07 | 1991-02-20 | Agent for plant growth promoting and inhibiting |
| FR9102282A FR2673181B1 (fr) | 1990-03-07 | 1991-02-26 | Phenylsulfonyltriazinyl-urees substituees, leurs sels et produit les contenant pour stimuler et inhiber la croissance des plantes. |
| CN91102096.9A CN1064388A (zh) | 1990-03-07 | 1991-03-05 | 用于促进和抑制植物生长的制剂 |
| GB9123657A GB2251613B (en) | 1990-03-07 | 1991-11-07 | Substituted phenylsulphoryltrianzinyl ureas, salts thereof and agent for plant growth stimulation and inhibition based thereon |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/SU1990/000067 WO1991013880A1 (en) | 1990-03-07 | 1990-03-07 | Substituted penylsulphonyltriazinylurea and salts thereof and means for stimulating and suppressing plant growth based on them |
| CA002036334A CA2036334C (en) | 1990-03-07 | 1991-02-14 | Substituted phenylsulphonyltriazinylureas, salts thereof and agent for plant growth stimulation and inhibition based thereon |
| CS91442A CS44291A3 (en) | 1990-03-07 | 1991-02-20 | Agent for plant growth promoting and inhibiting |
| CN91102096.9A CN1064388A (zh) | 1990-03-07 | 1991-03-05 | 用于促进和抑制植物生长的制剂 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1064388A true CN1064388A (zh) | 1992-09-16 |
Family
ID=27168867
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN91102096.9A Pending CN1064388A (zh) | 1990-03-07 | 1991-03-05 | 用于促进和抑制植物生长的制剂 |
Country Status (9)
| Country | Link |
|---|---|
| JP (1) | JPH05501415A (enrdf_load_stackoverflow) |
| CN (1) | CN1064388A (enrdf_load_stackoverflow) |
| AU (1) | AU631474B2 (enrdf_load_stackoverflow) |
| CA (1) | CA2036334C (enrdf_load_stackoverflow) |
| CH (1) | CH683341A5 (enrdf_load_stackoverflow) |
| CS (1) | CS44291A3 (enrdf_load_stackoverflow) |
| DE (2) | DE4092524T (enrdf_load_stackoverflow) |
| FR (1) | FR2673181B1 (enrdf_load_stackoverflow) |
| GB (1) | GB2251613B (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105439970A (zh) * | 2015-10-16 | 2016-03-30 | 南开大学 | 一类可控土壤降解速度的磺酰脲类新结构的发现与应用 |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2040180C1 (ru) * | 1992-09-04 | 1995-07-25 | Латвийская фирма "КАРЕ" | Гербицидный синергитический состав |
| WO2000044226A1 (de) * | 1999-01-27 | 2000-08-03 | Aventis Cropscience Gmbh | Formulierung von herbiziden |
| DE19963383A1 (de) | 1999-12-28 | 2001-07-05 | Aventis Cropscience Gmbh | Formulierung von Herbiziden und Pflanzenwachstumsregulatoren |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1082189A (en) * | 1976-04-07 | 1980-07-22 | George Levitt | Herbicidal sulfonamides |
| DK349479A (da) * | 1978-09-27 | 1980-03-28 | Du Pont | Sulfonamidderivater og deres anvendelse til regulering af plantevaekst |
| US4231784A (en) * | 1979-05-10 | 1980-11-04 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
| US4348219A (en) * | 1980-07-11 | 1982-09-07 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
| CS226915B1 (en) * | 1981-11-24 | 1984-04-16 | Varkonda Stefan | Plant growth regulating composition |
| US4780127A (en) * | 1982-03-25 | 1988-10-25 | Stauffer Chemical Company | Certain 2-(substituted benzoyl)-1,3-cyclohexanediones and their use as herbicides |
| ZA831626B (en) * | 1982-08-25 | 1983-11-30 | Velsicol Chemical Corp | New triazine compositions of matter |
| DE3322280A1 (de) * | 1983-06-16 | 1985-01-03 | Schering AG, 1000 Berlin und 4709 Bergkamen | Substituierte sulfonylharnstoffe, verfahren zur herstellung dieser verbindungen sowie diese enthaltende mittel mit herbizider und pflanzenwuchsregulierender wirkung |
| DE3413490A1 (de) * | 1984-04-10 | 1985-10-17 | Bayer Ag, 5090 Leverkusen | 2-(alkoximinoalkyloxycarbonyl)-phenylsulfonylharnstoffe |
| CA1257590A (en) * | 1984-06-07 | 1989-07-18 | Martha M. Bolinski | Herbicidal sulfonamides |
| DE3581428D1 (de) * | 1984-06-13 | 1991-02-28 | Roehm Gmbh | Verfahren zum ueberziehen von arzneiformen. |
| US4786316A (en) * | 1984-07-13 | 1988-11-22 | E. I. Du Pont De Nemours And Company | Herbicidal ortho-sulfamoyl sulfonamides |
| AU611191B2 (en) * | 1987-07-27 | 1991-06-06 | E.I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
| EP0336587B1 (en) * | 1988-03-24 | 1993-08-11 | E.I. Du Pont De Nemours And Company | Fluoroalkoxy amino triazines for control of weeds in sugar beets |
| JP2738010B2 (ja) * | 1988-07-15 | 1998-04-08 | 日産化学工業株式会社 | ピラゾール誘動体及び選択性除草剤 |
| JP2764931B2 (ja) * | 1988-08-05 | 1998-06-11 | 日産化学工業株式会社 | 安息香酸類の製法 |
-
1990
- 1990-03-07 AU AU68891/91A patent/AU631474B2/en not_active Ceased
- 1990-03-07 DE DE19904092524 patent/DE4092524T/de active Pending
- 1990-03-07 DE DE4092524A patent/DE4092524C2/de not_active Expired - Fee Related
- 1990-03-07 CH CH3286/91A patent/CH683341A5/de not_active IP Right Cessation
- 1990-03-07 JP JP3500742A patent/JPH05501415A/ja active Pending
-
1991
- 1991-02-14 CA CA002036334A patent/CA2036334C/en not_active Expired - Fee Related
- 1991-02-20 CS CS91442A patent/CS44291A3/cs unknown
- 1991-02-26 FR FR9102282A patent/FR2673181B1/fr not_active Expired - Fee Related
- 1991-03-05 CN CN91102096.9A patent/CN1064388A/zh active Pending
- 1991-11-07 GB GB9123657A patent/GB2251613B/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105439970A (zh) * | 2015-10-16 | 2016-03-30 | 南开大学 | 一类可控土壤降解速度的磺酰脲类新结构的发现与应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2673181B1 (fr) | 1994-02-11 |
| DE4092524T (enrdf_load_stackoverflow) | 1992-04-23 |
| FR2673181A1 (fr) | 1992-08-28 |
| DE4092524C2 (de) | 1996-09-12 |
| GB9123657D0 (en) | 1992-01-02 |
| CH683341A5 (de) | 1994-02-28 |
| AU6889191A (en) | 1991-10-10 |
| CA2036334C (en) | 1997-03-18 |
| GB2251613A (en) | 1992-07-15 |
| CA2036334A1 (en) | 1992-08-15 |
| JPH05501415A (ja) | 1993-03-18 |
| GB2251613B (en) | 1993-11-17 |
| CS44291A3 (en) | 1992-12-16 |
| AU631474B2 (en) | 1992-11-26 |
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