DE2140842A1 - 2-chloraethanphosphonsaeurederivate - Google Patents
2-chloraethanphosphonsaeurederivateInfo
- Publication number
- DE2140842A1 DE2140842A1 DE2140842A DE2140842A DE2140842A1 DE 2140842 A1 DE2140842 A1 DE 2140842A1 DE 2140842 A DE2140842 A DE 2140842A DE 2140842 A DE2140842 A DE 2140842A DE 2140842 A1 DE2140842 A1 DE 2140842A1
- Authority
- DE
- Germany
- Prior art keywords
- phosphonic acid
- chp
- parts
- chloroethane
- weight
- 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
Links
- IFVRMHVMSSPQLZ-UHFFFAOYSA-N P(O)(O)=O.ClCC Chemical class P(O)(O)=O.ClCC IFVRMHVMSSPQLZ-UHFFFAOYSA-N 0.000 title claims description 5
- 239000004480 active ingredient Substances 0.000 claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 15
- 230000012010 growth Effects 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- -1 alkyl radical Chemical class 0.000 claims description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 230000008635 plant growth Effects 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 2
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 150000003007 phosphonic acid derivatives Chemical class 0.000 claims description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 229940045713 antineoplastic alkylating drug ethylene imines Drugs 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 239000000243 solution Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 240000003768 Solanum lycopersicum Species 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 244000061176 Nicotiana tabacum Species 0.000 description 3
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 240000002024 Gossypium herbaceum Species 0.000 description 2
- 235000004341 Gossypium herbaceum Nutrition 0.000 description 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229960003237 betaine Drugs 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical compound CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
- OZDGMOYKSFPLSE-UHFFFAOYSA-N 2-Methylaziridine Chemical compound CC1CN1 OZDGMOYKSFPLSE-UHFFFAOYSA-N 0.000 description 1
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 244000277375 Raphia vinifera Species 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001541 aziridines Chemical class 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 229920003211 cis-1,4-polyisoprene Polymers 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 239000004615 ingredient Substances 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
- 125000000468 ketone group Chemical group 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004660 morphological change Effects 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000007921 spray Substances 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
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4071—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4075—Esters with hydroxyalkyl compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE787457D BE787457A (fr) | 1971-08-14 | Derives de l'acide chloro-2-ethanephosphonique | |
| DE2140842A DE2140842A1 (de) | 1971-08-14 | 1971-08-14 | 2-chloraethanphosphonsaeurederivate |
| JP47072634A JPS4826936A (enExample) | 1971-08-14 | 1972-07-21 | |
| IL39981A IL39981A (en) | 1971-08-14 | 1972-07-24 | 2-chloroethanephosphonic acid derivatives,their production and their use for regulating the growth of plants |
| US274579A US3867482A (en) | 1971-08-14 | 1972-07-24 | 2-Chloroethanephosphonic acid derivatives |
| PH13771*UA PH9332A (en) | 1971-08-14 | 1972-08-04 | 2-chloroethanephosphonic acid derivatives |
| BR5347/72A BR7205347D0 (pt) | 1971-08-14 | 1972-08-08 | Composicoes fitoreguladoras |
| GB3753272A GB1391093A (en) | 1971-08-14 | 1972-08-11 | 2-chloroethane-phosphonic acid derivatives |
| FR7229129A FR2149445B1 (enExample) | 1971-08-14 | 1972-08-11 | |
| IT5219372A IT962116B (it) | 1971-08-14 | 1972-08-14 | Derivati dell acido 2 cloroetan fosfonico |
| ES405854A ES405854A1 (es) | 1971-08-14 | 1972-08-14 | Procedimiento para la preparacion de derivados del acido 2-cloroetanofosfonico. |
| MY276/75A MY7500276A (en) | 1971-08-14 | 1975-12-30 | 2-chloroethanephosphonic acid derivatives |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2140842A DE2140842A1 (de) | 1971-08-14 | 1971-08-14 | 2-chloraethanphosphonsaeurederivate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2140842A1 true DE2140842A1 (de) | 1973-02-22 |
Family
ID=5816782
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2140842A Pending DE2140842A1 (de) | 1971-08-14 | 1971-08-14 | 2-chloraethanphosphonsaeurederivate |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US3867482A (enExample) |
| JP (1) | JPS4826936A (enExample) |
| BE (1) | BE787457A (enExample) |
| BR (1) | BR7205347D0 (enExample) |
| DE (1) | DE2140842A1 (enExample) |
| ES (1) | ES405854A1 (enExample) |
| FR (1) | FR2149445B1 (enExample) |
| GB (1) | GB1391093A (enExample) |
| IL (1) | IL39981A (enExample) |
| IT (1) | IT962116B (enExample) |
| MY (1) | MY7500276A (enExample) |
| PH (1) | PH9332A (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IN149593B (enExample) * | 1977-09-16 | 1982-02-06 | Gaf Corp | |
| FR2460111B2 (fr) * | 1979-06-29 | 1985-06-21 | Gaf Corp | Composition a base d'un melange aqueux de n-methyl-2-pyrrolidone et d'acide 2-halogenethylphosphonique et son application au traitement de plantes |
| AT379071B (de) * | 1982-07-19 | 1985-11-11 | Kretztechnik Gmbh | Schnittbildmechanik fuer ein ultraschallschnittbildgeraet |
| US11034708B2 (en) | 2017-04-11 | 2021-06-15 | Nippon Fine Chemical Co., Ltd. | Lipid derivative for nucleic acid introduction |
| EP4306531A4 (en) * | 2021-03-09 | 2025-02-19 | Nippon Fine Chemical Co., Ltd. | Phospholipid |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3507937A (en) * | 1966-10-04 | 1970-04-21 | Procter & Gamble | Reversed zwitterionic phosphorus compounds |
| US3666748A (en) * | 1967-12-18 | 1972-05-30 | Takeda Chemical Industries Ltd | Method for production of cytidine (or deoxycytidine)-5{40 -diphosphate choline and intermediates therefor |
-
0
- BE BE787457D patent/BE787457A/xx unknown
-
1971
- 1971-08-14 DE DE2140842A patent/DE2140842A1/de active Pending
-
1972
- 1972-07-21 JP JP47072634A patent/JPS4826936A/ja active Pending
- 1972-07-24 IL IL39981A patent/IL39981A/xx unknown
- 1972-07-24 US US274579A patent/US3867482A/en not_active Expired - Lifetime
- 1972-08-04 PH PH13771*UA patent/PH9332A/en unknown
- 1972-08-08 BR BR5347/72A patent/BR7205347D0/pt unknown
- 1972-08-11 GB GB3753272A patent/GB1391093A/en not_active Expired
- 1972-08-11 FR FR7229129A patent/FR2149445B1/fr not_active Expired
- 1972-08-14 IT IT5219372A patent/IT962116B/it active
- 1972-08-14 ES ES405854A patent/ES405854A1/es not_active Expired
-
1975
- 1975-12-30 MY MY276/75A patent/MY7500276A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BE787457A (fr) | 1973-02-12 |
| BR7205347D0 (pt) | 1973-05-31 |
| PH9332A (en) | 1975-09-23 |
| IL39981A0 (en) | 1972-09-28 |
| JPS4826936A (enExample) | 1973-04-09 |
| FR2149445B1 (enExample) | 1977-08-26 |
| GB1391093A (en) | 1975-04-16 |
| FR2149445A1 (enExample) | 1973-03-30 |
| IL39981A (en) | 1975-07-28 |
| MY7500276A (en) | 1975-12-31 |
| IT962116B (it) | 1973-12-20 |
| ES405854A1 (es) | 1976-06-01 |
| US3867482A (en) | 1975-02-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1643313A1 (de) | Neue herbicid wirksame Verbindungen und Zusammensetzungen | |
| DE2134146B2 (de) | Mittel zur Bekämpfung von pflanzenphatogenen Organismen auf Basis von Tetrazolo-(13cOchinolinverbindungen | |
| DE2140842A1 (de) | 2-chloraethanphosphonsaeurederivate | |
| DE1518333A1 (de) | N,N-substituierte 4-Methylsulfonyl-2,6-dinitroaniline und Verfahren zu ihrer Herstellung | |
| EP0036390A2 (de) | Diphenyläther-Harnstoffe mit herbizider Wirkung | |
| AT334134B (de) | Bekampfung von pilzschadlingen | |
| DE2813281C2 (de) | N-substituierte Bis-Carbamoyloximinodisulfidverbindungen, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Pestizide | |
| EP0013660A1 (de) | Aminoalkylester der 2-Nitro-5-(ortho-chlor-para-trifluor-methylphenoxy)-benzoesäure, deren Herstellung, sie als Wirkstoff enthaltende herbizide Mittel und deren Verwendung | |
| DE2524578C3 (de) | 5-Hydroxylaminomethylen-barbitursäurederivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbicide | |
| DE2114367A1 (de) | Organische Zinnverbindungen und Ver fahren zu ihrer Herstellung | |
| DE2101698A1 (de) | Substituierte m-Trifluormethylphenylharnstoffderivate | |
| CH468153A (de) | Insektenbekämpfungsmittel | |
| DE1906050C3 (de) | S-Alkyi-dnethyl-hexahydro-lHazepin)-1 -carbothiolate | |
| DE2356158C3 (de) | Herbicide Mittel mit einem Gehalt an Thiophosphorsäureamiden | |
| DE2408863A1 (de) | 2-chloraethanphosphonsaeurederivate | |
| DE1643482C3 (de) | Dithiophosphorigsäureester, deren Herstellung und Verwendung | |
| EP0029407A2 (de) | 1-N,N-Dimethylcarbamoyl-3(5)-alkyl-5(3)-alkoxyalkylthio-1,2,4-triazole, Verfahren zu ihrer Herstellung, diese Verbindungen enthaltende Mittel und ihre Verwendung zur Bekämpfung von Schädlingen sowie ihre Ausgangsprodukte und deren Herstellung | |
| DE3033358C2 (de) | Isovaleriansäure-Derivate, Verfahren zu deren Herstellung und diese enthaltende insektizide und acarizide Mittel | |
| DE1806120A1 (de) | Neue Carbamoyloxime,Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekaempfung von Schaedlingen | |
| DD236868A5 (de) | Mittel zum protahieren der wirkungsdauer und zur erhoehung der selektivitaet von herbiziden zusammensetzungen | |
| DE2147873A1 (de) | Organophosphor-Herbizide | |
| DE1567006C3 (de) | Unkrautbekämpfungsmittel | |
| DE2410131C3 (de) | Verfahren zur Herstellung von Organosulfinylmethyltriorganozinnverbindungen sowie Organosulfinylmethyltrl-(n-butyl)-zinnverbindungenund deren Verwendung in Schädlingsbekämpfungsmitteln | |
| DE1445946C (de) | O Methyl S alkyl S eckige Klammer auf 2,4 diamino s triazinyl (6) methyl eckige Klammer zu dithiophosphorsaureester | |
| DE1667986C3 (de) | Benzylthiophosphonsäure -O-alkyl-Sphenylester, Verfahren zu deren Herstellung und diese enthaltende Fungizide |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OHA | Expiration of time for request for examination |