SU584740A3 - Гербицидна композици - Google Patents
Гербицидна композициInfo
- Publication number
- SU584740A3 SU584740A3 SU7201829041A SU1829041A SU584740A3 SU 584740 A3 SU584740 A3 SU 584740A3 SU 7201829041 A SU7201829041 A SU 7201829041A SU 1829041 A SU1829041 A SU 1829041A SU 584740 A3 SU584740 A3 SU 584740A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- dioxane
- cis
- methyl
- phenyl
- benzyloxy
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title description 7
- 230000002363 herbicidal effect Effects 0.000 title description 5
- 239000004009 herbicide Substances 0.000 title 1
- -1 2-methylbenzyloxy Chemical group 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 229940126062 Compound A Drugs 0.000 description 2
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- DYLIWHYUXAJDOJ-OWOJBTEDSA-N (e)-4-(6-aminopurin-9-yl)but-2-en-1-ol Chemical compound NC1=NC=NC2=C1N=CN2C\C=C\CO DYLIWHYUXAJDOJ-OWOJBTEDSA-N 0.000 description 1
- VCKSNYNNVSOWEE-UHFFFAOYSA-N 1,3-dioxan-5-ol Chemical class OC1COCOC1 VCKSNYNNVSOWEE-UHFFFAOYSA-N 0.000 description 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
- OMTBMVJQYXLWAE-UHFFFAOYSA-N 2,5-diethyl-5-[(2-fluorophenyl)methoxy]-1,3-dioxane Chemical compound C1OC(CC)OCC1(CC)OCC1=CC=CC=C1F OMTBMVJQYXLWAE-UHFFFAOYSA-N 0.000 description 1
- BWYHAHQMECAMAR-UHFFFAOYSA-N 2-(bromomethyl)-5-phenylmethoxy-1,3-dioxane Chemical compound C1OC(CBr)OCC1OCC1=CC=CC=C1 BWYHAHQMECAMAR-UHFFFAOYSA-N 0.000 description 1
- GEASUTBFDRNQEF-UHFFFAOYSA-N 2-(chloromethyl)-5-phenylmethoxy-1,3-dioxane Chemical compound C1OC(CCl)OCC1OCC1=CC=CC=C1 GEASUTBFDRNQEF-UHFFFAOYSA-N 0.000 description 1
- IZTKYNPEPISCIY-UHFFFAOYSA-N 2-[(2-phenyl-1,3-dioxan-5-yl)oxymethyl]pyridine Chemical compound C=1C=CC=NC=1COC(CO1)COC1C1=CC=CC=C1 IZTKYNPEPISCIY-UHFFFAOYSA-N 0.000 description 1
- YOZVYJSSXPBWRF-UHFFFAOYSA-N 2-[(3-chlorophenoxy)methyl]-5-phenylmethoxy-1,3-dioxane Chemical compound ClC1=CC=CC(OCC2OCC(CO2)OCC=2C=CC=CC=2)=C1 YOZVYJSSXPBWRF-UHFFFAOYSA-N 0.000 description 1
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 1
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 1
- DBPWZXHTYAICLQ-UHFFFAOYSA-N 2-methyl-5-[(2-methylphenyl)methoxy]-1,3-dioxane Chemical compound C1OC(C)OCC1OCC1=CC=CC=C1C DBPWZXHTYAICLQ-UHFFFAOYSA-N 0.000 description 1
- JASINQNJRVUSBZ-UHFFFAOYSA-N 2-methyl-5-phenylmethoxy-1,3-dioxane Chemical compound C1OC(C)OCC1OCC1=CC=CC=C1 JASINQNJRVUSBZ-UHFFFAOYSA-N 0.000 description 1
- CWVCWKQSGCKPGT-UHFFFAOYSA-N 5-[(2-fluorophenyl)methoxy]-2-(methoxymethyl)-5-methyl-1,3-dioxane Chemical compound C1OC(COC)OCC1(C)OCC1=CC=CC=C1F CWVCWKQSGCKPGT-UHFFFAOYSA-N 0.000 description 1
- GMCAGELUBLAWJK-UHFFFAOYSA-N 5-[(2-fluorophenyl)methoxy]-2-phenyl-1,3-dioxane Chemical compound FC1=CC=CC=C1COC1COC(C=2C=CC=CC=2)OC1 GMCAGELUBLAWJK-UHFFFAOYSA-N 0.000 description 1
- KIYFILZSGCWDGD-UHFFFAOYSA-N 5-phenylmethoxy-2-(phenylmethoxymethyl)-1,3-dioxane Chemical compound O1CC(OCC=2C=CC=CC=2)COC1COCC1=CC=CC=C1 KIYFILZSGCWDGD-UHFFFAOYSA-N 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 244000299507 Gossypium hirsutum Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- 238000006359 acetalization reaction Methods 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- 150000005524 benzylchlorides Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
- C07D319/08—1,3-Dioxanes; Hydrogenated 1,3-dioxanes condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/14—Unsaturated ethers
- C07C43/178—Unsaturated ethers containing hydroxy or O-metal groups
- C07C43/1782—Unsaturated ethers containing hydroxy or O-metal groups containing six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US18240071A | 1971-09-21 | 1971-09-21 | |
| US22490972A | 1972-02-09 | 1972-02-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU584740A3 true SU584740A3 (ru) | 1977-12-15 |
Family
ID=26878066
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU7201829041A SU584740A3 (ru) | 1971-09-21 | 1972-09-19 | Гербицидна композици |
Country Status (23)
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1470509A (en) * | 1973-06-18 | 1977-04-14 | Shell Int Research | Dihalobenzyl ethers |
| US4035178A (en) * | 1976-08-31 | 1977-07-12 | Fmc Corporation | Herbicidal 1,3-dioxanes |
| IN146343B (enrdf_load_stackoverflow) * | 1976-08-31 | 1979-05-05 | Fmc Corp | |
| DE3176532D1 (de) * | 1981-12-01 | 1987-12-23 | Dow Chemical Co | 2-cyano-substituted 1,3-dioxane and dioxolane derivatives |
| DE3405914A1 (de) * | 1984-02-18 | 1985-08-22 | Merck Patent Gmbh, 6100 Darmstadt | Fluessigkristalline verbindungen |
| US4554011A (en) * | 1984-08-24 | 1985-11-19 | Chevron Research Company | Herbicidal 2S-(2β,4β,5β)-5-Arylmethoxy-4-substituted 2-alkyl-1,3-dioxane derivatives |
| DE10301110A1 (de) * | 2003-01-09 | 2004-07-22 | Bayer Cropscience Gmbh | Substituierte Benzoylderivate als Herbizide |
-
0
- BE BE789105D patent/BE789105A/xx unknown
-
1972
- 1972-08-22 CA CA149,950A patent/CA995679A/en not_active Expired
- 1972-08-24 IE IE1161/72A patent/IE36654B1/xx unknown
- 1972-08-29 IL IL40277A patent/IL40277A/xx unknown
- 1972-08-29 IL IL40227A patent/IL40227A0/xx unknown
- 1972-09-04 PH PH13863A patent/PH10389A/en unknown
- 1972-09-06 DE DE2243685A patent/DE2243685A1/de not_active Withdrawn
- 1972-09-14 AT AT1083573*7A patent/AT327604B/de not_active IP Right Cessation
- 1972-09-15 AR AR244107A patent/AR193292A1/es active
- 1972-09-19 OA OA54690A patent/OA04175A/xx unknown
- 1972-09-19 JP JP47093298A patent/JPS4839623A/ja active Pending
- 1972-09-19 SU SU7201829041A patent/SU584740A3/ru active
- 1972-09-19 ES ES406847A patent/ES406847A1/es not_active Expired
- 1972-09-20 NO NO3360/72A patent/NO137996C/no unknown
- 1972-09-20 CH CH1376172A patent/CH578302A5/xx not_active IP Right Cessation
- 1972-09-20 GB GB4345272A patent/GB1406849A/en not_active Expired
- 1972-09-20 BG BG7200021424A patent/BG23894A3/xx unknown
- 1972-09-20 TR TR17323A patent/TR17323A/xx unknown
- 1972-09-20 FR FR7233329A patent/FR2153344B1/fr not_active Expired
- 1972-09-20 DK DK463872AA patent/DK141367B/da unknown
- 1972-09-20 IT IT29452/72A patent/IT967673B/it active
- 1972-09-20 SE SE7212156A patent/SE398881B/xx unknown
- 1972-09-21 NL NL7212762A patent/NL7212762A/xx not_active Application Discontinuation
- 1972-09-21 RO RO7200072293A patent/RO62794A/ro unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE2243685A1 (de) | 1973-03-29 |
| FR2153344B1 (enrdf_load_stackoverflow) | 1977-07-29 |
| IL40277A (en) | 1977-10-31 |
| OA04175A (fr) | 1979-12-15 |
| NL7212762A (enrdf_load_stackoverflow) | 1973-03-23 |
| BE789105A (fr) | 1973-03-21 |
| DK141367B (da) | 1980-03-03 |
| IL40227A0 (en) | 1972-11-28 |
| CH578302A5 (enrdf_load_stackoverflow) | 1976-08-13 |
| SE398881B (sv) | 1978-01-23 |
| NO137996B (no) | 1978-02-27 |
| AT327604B (de) | 1976-02-10 |
| CA995679A (en) | 1976-08-24 |
| TR17323A (tr) | 1975-03-24 |
| ES406847A1 (es) | 1976-01-16 |
| IE36654B1 (en) | 1977-01-19 |
| AR193292A1 (es) | 1973-04-11 |
| GB1406849A (en) | 1975-09-17 |
| BG23894A3 (en) | 1977-11-10 |
| IE36654L (en) | 1973-03-21 |
| JPS4839623A (enrdf_load_stackoverflow) | 1973-06-11 |
| DK141367C (enrdf_load_stackoverflow) | 1980-09-22 |
| AU4613272A (en) | 1974-03-07 |
| RO62794A (fr) | 1977-11-15 |
| NO137996C (no) | 1978-06-07 |
| PH10389A (en) | 1977-03-04 |
| IT967673B (it) | 1974-03-11 |
| ATA1083573A (de) | 1975-04-15 |
| FR2153344A1 (enrdf_load_stackoverflow) | 1973-05-04 |
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