NO802503L - Benzothiazolethanimidamider som plantevekstregulerende midler. - Google Patents
Benzothiazolethanimidamider som plantevekstregulerende midler.Info
- Publication number
- NO802503L NO802503L NO802503A NO802503A NO802503L NO 802503 L NO802503 L NO 802503L NO 802503 A NO802503 A NO 802503A NO 802503 A NO802503 A NO 802503A NO 802503 L NO802503 L NO 802503L
- Authority
- NO
- Norway
- Prior art keywords
- plant
- plants
- compounds
- plant growth
- halogen
- Prior art date
Links
- 239000005648 plant growth regulator Substances 0.000 title description 3
- 238000002360 preparation method Methods 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 15
- WEVYAHXRMPXWCK-UHFFFAOYSA-N methyl cyanide Natural products CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 8
- 230000001105 regulatory effect Effects 0.000 claims description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical group 0.000 claims description 7
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000005864 Sulphur Chemical group 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- 150000007960 acetonitrile Chemical class 0.000 claims description 3
- 239000000969 carrier Substances 0.000 claims description 3
- 239000003085 diluting agent Substances 0.000 claims description 3
- 230000012010 growth Effects 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 36
- 239000004480 active ingredient Substances 0.000 description 10
- 244000068988 Glycine max Species 0.000 description 7
- 230000004048 modification Effects 0.000 description 7
- 238000012986 modification Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 230000008635 plant growth Effects 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 235000010469 Glycine max Nutrition 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 230000018109 developmental process Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 235000021374 legumes Nutrition 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 230000004044 response Effects 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-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
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 230000033228 biological regulation Effects 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 239000001963 growth medium Substances 0.000 description 2
- 230000000051 modifying effect Effects 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- SIMWFXSMDQBKED-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yl)acetamide Chemical class C1=CC=C2SC(CC(=O)N)=NC2=C1 SIMWFXSMDQBKED-UHFFFAOYSA-N 0.000 description 1
- BCIJDSPGUOFPAI-UHFFFAOYSA-N 2-(2-sulfanylidene-1,3-benzothiazol-3-yl)acetonitrile Chemical class C1=CC=C2N(CC#N)C(=S)SC2=C1 BCIJDSPGUOFPAI-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 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
- 240000007049 Juglans regia Species 0.000 description 1
- 235000009496 Juglans regia Nutrition 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N alpha-methyl toluene Natural products CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000009286 beneficial effect Effects 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
- -1 calcareous earth Substances 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000029553 photosynthesis Effects 0.000 description 1
- 238000010672 photosynthesis Methods 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 231100000208 phytotoxic Toxicity 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 230000008121 plant development Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000005549 size reduction Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 230000005068 transpiration Effects 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D277/70—Sulfur atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- 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)
- Thiazole And Isothizaole Compounds (AREA)
- Cultivation Of Plants (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/068,993 US4283220A (en) | 1979-08-23 | 1979-08-23 | Imidamides derived from 2-oxo-3-benzothiazoline acetic acid plant growth regulants |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO802503L true NO802503L (no) | 1981-02-24 |
Family
ID=22086018
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO802503A NO802503L (no) | 1979-08-23 | 1980-08-22 | Benzothiazolethanimidamider som plantevekstregulerende midler. |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US4283220A (cs) |
| EP (1) | EP0024889A1 (cs) |
| JP (1) | JPS5677270A (cs) |
| KR (1) | KR840001933B1 (cs) |
| AR (1) | AR224418A1 (cs) |
| AU (1) | AU530437B2 (cs) |
| BG (1) | BG31502A3 (cs) |
| BR (1) | BR8005341A (cs) |
| CA (1) | CA1148959A (cs) |
| CS (1) | CS214840B2 (cs) |
| DD (1) | DD152902A5 (cs) |
| DK (1) | DK361480A (cs) |
| FI (1) | FI802660A7 (cs) |
| IL (1) | IL60895A (cs) |
| IN (1) | IN153446B (cs) |
| NO (1) | NO802503L (cs) |
| NZ (1) | NZ194736A (cs) |
| PL (1) | PL226365A1 (cs) |
| YU (1) | YU202580A (cs) |
| ZA (1) | ZA805182B (cs) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH04217579A (ja) * | 1990-12-13 | 1992-08-07 | Mitsubishi Electric Corp | エレベータロープの横揺れ防止装置 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1792770A (en) * | 1924-11-18 | 1931-02-17 | Goodyear Tire & Rubber | Vulcanization of rubber and method of producing same |
| US2947782A (en) * | 1957-12-23 | 1960-08-02 | Rohm & Haas | Aminoacetamidoximes |
| NL108409C (cs) * | 1958-10-29 | |||
| US3717690A (en) * | 1970-07-01 | 1973-02-20 | Exxon Research Engineering Co | N,n-dialkylamidoxime phosphates |
| US3923491A (en) * | 1973-08-09 | 1975-12-02 | Allied Chem | Growth regulants for plants |
| JPS577122B2 (cs) * | 1973-12-24 | 1982-02-09 | ||
| US4049419A (en) * | 1975-05-12 | 1977-09-20 | Monsanto Company | Use of benzothiazoline compounds as plant growth regulants |
| US3993468A (en) * | 1975-05-12 | 1976-11-23 | Monsanto Company | Use of 3-substituted benzothiazolines as plant growth regulants |
| US4075216A (en) * | 1976-10-26 | 1978-02-21 | Monsanto Company | Certain benzothiazolin-2-one derivatives |
-
1979
- 1979-08-23 US US06/068,993 patent/US4283220A/en not_active Expired - Lifetime
-
1980
- 1980-08-12 YU YU02025/80A patent/YU202580A/xx unknown
- 1980-08-21 AR AR282243A patent/AR224418A1/es active
- 1980-08-21 EP EP80302897A patent/EP0024889A1/en not_active Withdrawn
- 1980-08-21 KR KR1019800003304A patent/KR840001933B1/ko not_active Expired
- 1980-08-22 CA CA000358958A patent/CA1148959A/en not_active Expired
- 1980-08-22 JP JP11488080A patent/JPS5677270A/ja active Pending
- 1980-08-22 IN IN963/CAL/80A patent/IN153446B/en unknown
- 1980-08-22 AU AU61679/80A patent/AU530437B2/en not_active Ceased
- 1980-08-22 FI FI802660A patent/FI802660A7/fi not_active Application Discontinuation
- 1980-08-22 CS CS805769A patent/CS214840B2/cs unknown
- 1980-08-22 BG BG048910A patent/BG31502A3/xx unknown
- 1980-08-22 PL PL22636580A patent/PL226365A1/xx unknown
- 1980-08-22 IL IL60895A patent/IL60895A/xx unknown
- 1980-08-22 ZA ZA00805182A patent/ZA805182B/xx unknown
- 1980-08-22 DD DD80223460A patent/DD152902A5/de unknown
- 1980-08-22 DK DK361480A patent/DK361480A/da not_active Application Discontinuation
- 1980-08-22 NO NO802503A patent/NO802503L/no unknown
- 1980-08-22 NZ NZ194736A patent/NZ194736A/xx unknown
- 1980-08-22 BR BR8005341A patent/BR8005341A/pt unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL60895A (en) | 1983-11-30 |
| BR8005341A (pt) | 1981-03-04 |
| ZA805182B (en) | 1981-09-30 |
| KR830003451A (ko) | 1983-06-20 |
| IN153446B (cs) | 1984-07-14 |
| BG31502A3 (bg) | 1982-01-15 |
| JPS5677270A (en) | 1981-06-25 |
| KR840001933B1 (ko) | 1984-10-25 |
| AU6167980A (en) | 1981-03-05 |
| IL60895A0 (en) | 1980-10-26 |
| CS214840B2 (en) | 1982-06-25 |
| US4283220A (en) | 1981-08-11 |
| DK361480A (da) | 1981-02-24 |
| PL226365A1 (cs) | 1981-06-05 |
| CA1148959A (en) | 1983-06-28 |
| YU202580A (en) | 1983-04-30 |
| AR224418A1 (es) | 1981-11-30 |
| DD152902A5 (de) | 1981-12-16 |
| AU530437B2 (en) | 1983-07-14 |
| EP0024889A1 (en) | 1981-03-11 |
| FI802660A7 (fi) | 1981-02-23 |
| NZ194736A (en) | 1983-02-15 |
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