DE1745901A1 - Herbizide - Google Patents
HerbizideInfo
- Publication number
- DE1745901A1 DE1745901A1 DE19651745901 DE1745901A DE1745901A1 DE 1745901 A1 DE1745901 A1 DE 1745901A1 DE 19651745901 DE19651745901 DE 19651745901 DE 1745901 A DE1745901 A DE 1745901A DE 1745901 A1 DE1745901 A1 DE 1745901A1
- Authority
- DE
- Germany
- Prior art keywords
- dioxo
- chlorine
- group
- decahydroquinazoline
- isopropyl
- 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
- 239000004009 herbicide Substances 0.000 title claims description 4
- 239000000460 chlorine Substances 0.000 claims description 12
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 230000002363 herbicidal effect Effects 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 241000196324 Embryophyta Species 0.000 description 10
- 240000006122 Chenopodium album Species 0.000 description 9
- 240000006694 Stellaria media Species 0.000 description 9
- 239000004480 active ingredient Substances 0.000 description 8
- -1 3-propyl- Chemical group 0.000 description 7
- 240000004153 Hibiscus sabdariffa Species 0.000 description 6
- 235000001018 Hibiscus sabdariffa Nutrition 0.000 description 6
- 235000005291 Rumex acetosa Nutrition 0.000 description 6
- 244000152045 Themeda triandra Species 0.000 description 6
- 235000003513 sheep sorrel Nutrition 0.000 description 6
- 235000009344 Chenopodium album Nutrition 0.000 description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
- 240000001592 Amaranthus caudatus Species 0.000 description 4
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 4
- 235000011498 Chenopodium album var missouriense Nutrition 0.000 description 4
- 235000013328 Chenopodium album var. album Nutrition 0.000 description 4
- 235000014052 Chenopodium album var. microphyllum Nutrition 0.000 description 4
- 235000014050 Chenopodium album var. stevensii Nutrition 0.000 description 4
- 235000013012 Chenopodium album var. striatum Nutrition 0.000 description 4
- 244000042664 Matricaria chamomilla Species 0.000 description 4
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 4
- 244000292693 Poa annua Species 0.000 description 4
- 241000219053 Rumex Species 0.000 description 4
- 240000008042 Zea mays Species 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 244000024671 Brassica kaber Species 0.000 description 3
- 241001518935 Eragrostis Species 0.000 description 3
- 235000009108 Urtica dioica Nutrition 0.000 description 3
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 3
- 241001621841 Alopecurus myosuroides Species 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000219198 Brassica Species 0.000 description 2
- 235000003351 Brassica cretica Nutrition 0.000 description 2
- 235000003343 Brassica rupestris Nutrition 0.000 description 2
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 2
- 235000011305 Capsella bursa pastoris Nutrition 0.000 description 2
- 240000008867 Capsella bursa-pastoris Species 0.000 description 2
- 235000007866 Chamaemelum nobile Nutrition 0.000 description 2
- 240000005702 Galium aparine Species 0.000 description 2
- 235000014820 Galium aparine Nutrition 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- 241000220261 Sinapis Species 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- 244000274883 Urtica dioica Species 0.000 description 2
- 235000007244 Zea mays Nutrition 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 244000038559 crop plants Species 0.000 description 2
- 230000000977 initiatory effect Effects 0.000 description 2
- 235000010460 mustard Nutrition 0.000 description 2
- 235000012015 potatoes Nutrition 0.000 description 2
- HZNXIPDYYIWDNM-UHFFFAOYSA-N 1,2,3,4,4a,5,6,7,8,8a-decahydroquinazoline Chemical compound N1CNCC2CCCCC21 HZNXIPDYYIWDNM-UHFFFAOYSA-N 0.000 description 1
- USQHEVWOPJDAAX-UHFFFAOYSA-N 2-azaniumylcyclohexane-1-carboxylate Chemical compound NC1CCCCC1C(O)=O USQHEVWOPJDAAX-UHFFFAOYSA-N 0.000 description 1
- CPUAQUMVDXYDTN-UHFFFAOYSA-N 3-propan-2-yl-4a,5,6,7,8,8a-hexahydro-1h-quinazoline-2,4-dione Chemical compound C1CCCC2C(=O)N(C(C)C)C(=O)NC21 CPUAQUMVDXYDTN-UHFFFAOYSA-N 0.000 description 1
- 241000743985 Alopecurus Species 0.000 description 1
- 235000008427 Brassica arvensis Nutrition 0.000 description 1
- 235000005637 Brassica campestris Nutrition 0.000 description 1
- 235000014750 Brassica kaber Nutrition 0.000 description 1
- 235000011292 Brassica rapa Nutrition 0.000 description 1
- 235000010149 Brassica rapa subsp chinensis Nutrition 0.000 description 1
- 235000010570 Brassica rapa var. rapa Nutrition 0.000 description 1
- 241001260012 Bursa Species 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000209210 Dactylis Species 0.000 description 1
- 244000058871 Echinochloa crus-galli Species 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 241000288105 Grus Species 0.000 description 1
- 241001456088 Hesperocnide Species 0.000 description 1
- 235000017945 Matricaria Nutrition 0.000 description 1
- 241000209117 Panicum Species 0.000 description 1
- 235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 1
- 235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000002634 Solanum Nutrition 0.000 description 1
- 241000207763 Solanum Species 0.000 description 1
- 244000062793 Sorghum vulgare Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 241000219422 Urtica Species 0.000 description 1
- 241001148683 Zostera marina Species 0.000 description 1
- 150000001263 acyl chlorides Chemical class 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 235000002020 sage Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/95—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
- C07D239/96—Two oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB0084324 | 1965-10-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1745901A1 true DE1745901A1 (de) | 1969-10-16 |
Family
ID=6982381
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19651745901 Pending DE1745901A1 (de) | 1965-10-30 | 1965-10-30 | Herbizide |
Country Status (10)
-
1965
- 1965-10-30 DE DE19651745901 patent/DE1745901A1/de active Pending
-
1966
- 1966-10-03 IL IL26619A patent/IL26619A/en unknown
- 1966-10-12 CH CH1471866A patent/CH481574A/de not_active IP Right Cessation
- 1966-10-24 BR BR183945/66A patent/BR6683945D0/pt unknown
- 1966-10-24 BE BE688789D patent/BE688789A/xx unknown
- 1966-10-28 AT AT1004966A patent/AT267251B/de active
- 1966-10-28 GB GB48420/66A patent/GB1159543A/en not_active Expired
- 1966-10-28 NL NL6615301A patent/NL6615301A/xx unknown
- 1966-10-28 DK DK561466AA patent/DK115803B/da unknown
- 1966-10-29 ES ES0332903A patent/ES332903A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| AT267251B (de) | 1968-12-27 |
| CH481574A (de) | 1969-11-30 |
| NL6615301A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1967-05-02 |
| BR6683945D0 (pt) | 1973-12-04 |
| GB1159543A (en) | 1969-07-30 |
| ES332903A1 (es) | 1967-11-16 |
| BE688789A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1967-04-24 |
| IL26619A (en) | 1971-04-28 |
| DK115803B (da) | 1969-11-10 |
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