NL7906888A - Gesubstitueerde thiosemicarbaziden, werkwijze voor het bereiden ervan alsmede preparaat en werkwijze voor het regelen van de plantengroei. - Google Patents
Gesubstitueerde thiosemicarbaziden, werkwijze voor het bereiden ervan alsmede preparaat en werkwijze voor het regelen van de plantengroei. Download PDFInfo
- Publication number
- NL7906888A NL7906888A NL7906888A NL7906888A NL7906888A NL 7906888 A NL7906888 A NL 7906888A NL 7906888 A NL7906888 A NL 7906888A NL 7906888 A NL7906888 A NL 7906888A NL 7906888 A NL7906888 A NL 7906888A
- Authority
- NL
- Netherlands
- Prior art keywords
- group
- carbon atoms
- formula
- methyl
- alkyl
- Prior art date
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- 238000002360 preparation method Methods 0.000 title claims description 31
- 238000000034 method Methods 0.000 title claims description 22
- 230000008635 plant growth Effects 0.000 title description 18
- 150000003583 thiosemicarbazides Chemical class 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims description 84
- 125000004432 carbon atom Chemical group C* 0.000 claims description 63
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- -1 haloalkyl ester Chemical class 0.000 claims description 28
- 150000003839 salts Chemical class 0.000 claims description 27
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 26
- 230000012010 growth Effects 0.000 claims description 24
- 150000002148 esters Chemical class 0.000 claims description 19
- 239000000460 chlorine Substances 0.000 claims description 18
- 239000004480 active ingredient Substances 0.000 claims description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- OWKWAVBMKKZMHE-UHFFFAOYSA-N benzamidothiourea Chemical compound NC(=S)NNC(=O)C1=CC=CC=C1 OWKWAVBMKKZMHE-UHFFFAOYSA-N 0.000 claims description 7
- 229910052731 fluorine Inorganic materials 0.000 claims description 7
- 125000005843 halogen group Chemical group 0.000 claims description 7
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims description 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 7
- XLQAGHXOQYTWGK-UHFFFAOYSA-N 2-[[methyl(phenylcarbamothioyl)amino]carbamoyl]benzoic acid Chemical compound C=1C=CC=CC=1NC(=S)N(C)NC(=O)C1=CC=CC=C1C(O)=O XLQAGHXOQYTWGK-UHFFFAOYSA-N 0.000 claims description 6
- 125000005907 alkyl ester group Chemical group 0.000 claims description 6
- 150000003863 ammonium salts Chemical class 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 5
- 239000011737 fluorine Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 125000001624 naphthyl group Chemical group 0.000 claims description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 4
- 239000002671 adjuvant Substances 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 4
- 125000005427 anthranyl group Chemical group 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 125000005561 phenanthryl group Chemical group 0.000 claims description 4
- 229910052700 potassium Inorganic materials 0.000 claims description 4
- 239000011591 potassium Substances 0.000 claims description 4
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- QJQYPZZUKLQGGT-UHFFFAOYSA-N methyl hypobromite Chemical compound COBr QJQYPZZUKLQGGT-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
- 125000005081 alkoxyalkoxyalkyl group Chemical group 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- XEVRDFDBXJMZFG-UHFFFAOYSA-N carbonyl dihydrazine Chemical compound NNC(=O)NN XEVRDFDBXJMZFG-UHFFFAOYSA-N 0.000 claims description 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 2
- 150000003021 phthalic acid derivatives Chemical class 0.000 claims description 2
- 230000008569 process Effects 0.000 claims description 2
- 125000006413 ring segment Chemical group 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 60
- 239000000203 mixture Substances 0.000 description 54
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 35
- 230000000694 effects Effects 0.000 description 33
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 21
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 21
- 239000007921 spray Substances 0.000 description 21
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 19
- 239000000047 product Substances 0.000 description 16
- 239000007787 solid Substances 0.000 description 16
- 238000011282 treatment Methods 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- RSPISYXLHRIGJD-UHFFFAOYSA-N OOOO Chemical compound OOOO RSPISYXLHRIGJD-UHFFFAOYSA-N 0.000 description 15
- 239000002904 solvent Substances 0.000 description 13
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 11
- 239000002689 soil Substances 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 10
- PCWYQDWBLWIBBB-UHFFFAOYSA-N methyl 2-[[methyl(phenylcarbamothioyl)amino]carbamoyl]benzoate Chemical compound COC(=O)C1=CC=CC=C1C(=O)NN(C)C(=S)NC1=CC=CC=C1 PCWYQDWBLWIBBB-UHFFFAOYSA-N 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 238000009472 formulation Methods 0.000 description 9
- 238000002844 melting Methods 0.000 description 9
- 230000008018 melting Effects 0.000 description 9
- 239000004094 surface-active agent Substances 0.000 description 9
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 8
- 239000007859 condensation product Substances 0.000 description 8
- 230000001276 controlling effect Effects 0.000 description 8
- 239000003995 emulsifying agent Substances 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 235000019198 oils Nutrition 0.000 description 8
- 159000000000 sodium salts Chemical class 0.000 description 8
- 239000002270 dispersing agent Substances 0.000 description 7
- 235000010469 Glycine max Nutrition 0.000 description 6
- KUGRPPRAQNPSQD-UHFFFAOYSA-N OOOOO Chemical compound OOOOO KUGRPPRAQNPSQD-UHFFFAOYSA-N 0.000 description 6
- RTYZCUMXOXNVSI-UHFFFAOYSA-N OOOOOOOOOOOOOOOOOO Chemical compound OOOOOOOOOOOOOOOOOO RTYZCUMXOXNVSI-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 235000013399 edible fruits Nutrition 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
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- 125000001557 phthalyl group Chemical group C(=O)(O)C1=C(C(=O)*)C=CC=C1 0.000 description 5
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- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
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- 239000007788 liquid Substances 0.000 description 4
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 4
- 235000019796 monopotassium phosphate Nutrition 0.000 description 4
- QKFJKGMPGYROCL-UHFFFAOYSA-N phenyl isothiocyanate Chemical compound S=C=NC1=CC=CC=C1 QKFJKGMPGYROCL-UHFFFAOYSA-N 0.000 description 4
- PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 description 4
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- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
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- KRZBCHWVBQOTNZ-RDJMKVHDSA-N (3r,5r)-3,5-bis[[(e)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy]-1,4-dihydroxycyclohexane-1-carboxylic acid Chemical compound O([C@@H]1CC(O)(C[C@H](C1O)OC(=O)\C=C\C=1C=C(O)C(O)=CC=1)C(O)=O)C(=O)\C=C\C1=CC=C(O)C(O)=C1 KRZBCHWVBQOTNZ-RDJMKVHDSA-N 0.000 description 2
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- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
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- 101100334117 Caenorhabditis elegans fah-1 gene Proteins 0.000 description 2
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- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
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- KJAQRHMKLVGSCG-UHFFFAOYSA-N propan-2-ylhydrazine Chemical compound CC(C)NN KJAQRHMKLVGSCG-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/192—Radicals derived from carboxylic acids from aromatic carboxylic acids
-
- 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<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Quinoline Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US94223278A | 1978-09-14 | 1978-09-14 | |
| US94223278 | 1978-09-14 | ||
| US85179A | 1979-01-03 | 1979-01-03 | |
| US85179 | 1979-01-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL7906888A true NL7906888A (nl) | 1980-03-18 |
Family
ID=26668228
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL7906888A NL7906888A (nl) | 1978-09-14 | 1979-09-14 | Gesubstitueerde thiosemicarbaziden, werkwijze voor het bereiden ervan alsmede preparaat en werkwijze voor het regelen van de plantengroei. |
Country Status (32)
| Country | Link |
|---|---|
| EP (1) | EP0009324B1 (enExample) |
| JP (1) | JPS5551057A (enExample) |
| AR (1) | AR224370A1 (enExample) |
| AT (1) | AT371973B (enExample) |
| AU (1) | AU521387B2 (enExample) |
| BE (1) | BE878668A (enExample) |
| BR (1) | BR7905801A (enExample) |
| CA (1) | CA1127167A (enExample) |
| CS (1) | CS209934B2 (enExample) |
| DD (2) | DD145995A5 (enExample) |
| DE (1) | DE2963370D1 (enExample) |
| DK (1) | DK338179A (enExample) |
| ES (1) | ES484143A1 (enExample) |
| FI (1) | FI792803A7 (enExample) |
| FR (1) | FR2436139A1 (enExample) |
| GB (1) | GB2030565B (enExample) |
| GR (1) | GR69827B (enExample) |
| IL (1) | IL58090A0 (enExample) |
| IS (1) | IS2508A7 (enExample) |
| IT (1) | IT1123136B (enExample) |
| LU (1) | LU81682A1 (enExample) |
| MA (1) | MA18579A1 (enExample) |
| MW (1) | MW2579A1 (enExample) |
| NL (1) | NL7906888A (enExample) |
| NO (1) | NO792955L (enExample) |
| NZ (1) | NZ191309A (enExample) |
| PL (1) | PL218244A1 (enExample) |
| PT (1) | PT70094A (enExample) |
| RO (1) | RO78609A (enExample) |
| YU (1) | YU219379A (enExample) |
| ZA (1) | ZA794495B (enExample) |
| ZW (1) | ZW16379A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4405791A (en) * | 1979-12-10 | 1983-09-20 | Gulf Oil Corporation | Arylthioureido pyridinecarbamino compounds and use as plant growth regulants |
| US4272279A (en) * | 1980-06-19 | 1981-06-09 | Gulf Oil Corporation | Semicarbazidyl phthalides and use as plant growth regulators |
| WO1989006125A1 (en) * | 1987-12-31 | 1989-07-13 | Smithkline Beckman Corporation | 4-aralkyl-5-substituted-1,2,4-triazole-5-thiols |
| IT221762Z2 (it) * | 1991-03-25 | 1994-10-20 | Salvatore Sapienza | Siringa opaca |
| US8486863B2 (en) | 2006-11-23 | 2013-07-16 | Vib Vzw | Activators of lateral root formation |
| JPWO2025005176A1 (enExample) * | 2023-06-30 | 2025-01-02 | ||
| CN119462460A (zh) * | 2024-11-18 | 2025-02-18 | 洛阳冠银生物科技有限公司 | 一种有机酸银酰基硫脲配合物及其制备方法和应用 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2097737A5 (en) * | 1970-07-14 | 1972-03-03 | Berlin Chemie Veb | Virustatic 4-substd 1-acylthiosemicarbazides -from carboxylic acid - hydrazide and isothiocyanates or from carboxylic acid chloride and 4- |
| US3836350A (en) * | 1971-10-20 | 1974-09-17 | Du Pont | Ureidotriazoles as yield increasing agents for crop plants |
| US3912496A (en) * | 1972-09-29 | 1975-10-14 | Du Pont | Ureidotriazoles as cytokinins and plant antisenescence agents |
-
1979
- 1979-08-13 GR GR59824A patent/GR69827B/el unknown
- 1979-08-13 DK DK338179A patent/DK338179A/da unknown
- 1979-08-14 NZ NZ191309A patent/NZ191309A/xx unknown
- 1979-08-15 CA CA333,812A patent/CA1127167A/en not_active Expired
- 1979-08-20 GB GB7928951A patent/GB2030565B/en not_active Expired
- 1979-08-20 DE DE7979301694T patent/DE2963370D1/de not_active Expired
- 1979-08-20 IS IS2508A patent/IS2508A7/is unknown
- 1979-08-20 EP EP79301694A patent/EP0009324B1/en not_active Expired
- 1979-08-21 PT PT70094A patent/PT70094A/pt unknown
- 1979-08-22 IL IL58090A patent/IL58090A0/xx unknown
- 1979-08-24 ZA ZA00794495A patent/ZA794495B/xx unknown
- 1979-08-24 AU AU50276/79A patent/AU521387B2/en not_active Ceased
- 1979-08-28 ZW ZW163/79A patent/ZW16379A1/xx unknown
- 1979-08-29 MW MW25/79A patent/MW2579A1/xx unknown
- 1979-09-06 MA MA18779A patent/MA18579A1/fr unknown
- 1979-09-06 RO RO7998616A patent/RO78609A/ro unknown
- 1979-09-07 BE BE0/197057A patent/BE878668A/fr unknown
- 1979-09-07 AR AR277983A patent/AR224370A1/es active
- 1979-09-10 FI FI792803A patent/FI792803A7/fi not_active Application Discontinuation
- 1979-09-10 YU YU02193/79A patent/YU219379A/xx unknown
- 1979-09-10 AT AT0594879A patent/AT371973B/de not_active IP Right Cessation
- 1979-09-11 PL PL21824479A patent/PL218244A1/xx unknown
- 1979-09-11 CS CS796151A patent/CS209934B2/cs unknown
- 1979-09-11 BR BR7905801A patent/BR7905801A/pt unknown
- 1979-09-12 NO NO792955A patent/NO792955L/no unknown
- 1979-09-12 LU LU81682A patent/LU81682A1/fr unknown
- 1979-09-12 IT IT25674/79A patent/IT1123136B/it active
- 1979-09-13 DD DD79215526A patent/DD145995A5/de unknown
- 1979-09-13 ES ES484143A patent/ES484143A1/es not_active Expired
- 1979-09-13 DD DD79223332A patent/DD153832A5/de unknown
- 1979-09-13 FR FR7922929A patent/FR2436139A1/fr not_active Withdrawn
- 1979-09-14 NL NL7906888A patent/NL7906888A/nl not_active Application Discontinuation
- 1979-09-14 JP JP11746579A patent/JPS5551057A/ja active Pending
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| BA | A request for search or an international-type search has been filed | ||
| BV | The patent application has lapsed |