DE1200062B - Herbizid - Google Patents
HerbizidInfo
- Publication number
- DE1200062B DE1200062B DEB75134A DEB0075134A DE1200062B DE 1200062 B DE1200062 B DE 1200062B DE B75134 A DEB75134 A DE B75134A DE B0075134 A DEB0075134 A DE B0075134A DE 1200062 B DE1200062 B DE 1200062B
- Authority
- DE
- Germany
- Prior art keywords
- hexahydro
- methanoindanyl
- mixture
- isomers
- urea
- 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
- 230000002363 herbicidal effect Effects 0.000 title claims description 9
- 239000004009 herbicide Substances 0.000 title claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 125000000480 butynyl group Chemical group [*]C#CC([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 16
- 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 14
- 241000219873 Vicia Species 0.000 description 11
- 240000006694 Stellaria media Species 0.000 description 10
- 241000196324 Embryophyta Species 0.000 description 7
- 240000001592 Amaranthus caudatus Species 0.000 description 6
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 6
- 240000008042 Zea mays Species 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 6
- 239000004202 carbamide Substances 0.000 description 6
- 235000013877 carbamide Nutrition 0.000 description 6
- 241000287828 Gallus gallus Species 0.000 description 5
- 240000005979 Hordeum vulgare Species 0.000 description 5
- 244000292693 Poa annua Species 0.000 description 5
- 244000062793 Sorghum vulgare Species 0.000 description 5
- 235000019713 millet Nutrition 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- 241000219146 Gossypium Species 0.000 description 4
- 235000007340 Hordeum vulgare Nutrition 0.000 description 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 4
- 229920005552 sodium lignosulfonate Polymers 0.000 description 4
- 150000003672 ureas Chemical class 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 241001621841 Alopecurus myosuroides Species 0.000 description 3
- 244000105624 Arachis hypogaea Species 0.000 description 3
- 235000007320 Avena fatua Nutrition 0.000 description 3
- 241000219198 Brassica Species 0.000 description 3
- 235000003351 Brassica cretica Nutrition 0.000 description 3
- 235000003343 Brassica rupestris Nutrition 0.000 description 3
- 244000088461 Panicum crus-galli Species 0.000 description 3
- 235000011999 Panicum crusgalli Nutrition 0.000 description 3
- 240000004713 Pisum sativum Species 0.000 description 3
- 235000010582 Pisum sativum Nutrition 0.000 description 3
- 244000137827 Rumex acetosa Species 0.000 description 3
- 235000005291 Rumex acetosa Nutrition 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 235000010460 mustard Nutrition 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 244000075850 Avena orientalis Species 0.000 description 2
- 235000006463 Brassica alba Nutrition 0.000 description 2
- 244000140786 Brassica hirta Species 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 235000001018 Hibiscus sabdariffa Nutrition 0.000 description 2
- 241000520028 Lamium Species 0.000 description 2
- 241000209082 Lolium Species 0.000 description 2
- 240000004296 Lolium perenne Species 0.000 description 2
- 244000042664 Matricaria chamomilla Species 0.000 description 2
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 235000005373 Uvularia sessilifolia Nutrition 0.000 description 2
- 235000007244 Zea mays Nutrition 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 235000011655 cotton Nutrition 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 235000020232 peanut Nutrition 0.000 description 2
- 235000003513 sheep sorrel Nutrition 0.000 description 2
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 241000209764 Avena fatua Species 0.000 description 1
- 235000005637 Brassica campestris Nutrition 0.000 description 1
- 235000014750 Brassica kaber Nutrition 0.000 description 1
- 240000008100 Brassica rapa Species 0.000 description 1
- 235000010149 Brassica rapa subsp chinensis Nutrition 0.000 description 1
- 235000010570 Brassica rapa var. rapa Nutrition 0.000 description 1
- 235000007866 Chamaemelum nobile Nutrition 0.000 description 1
- 244000239348 Echinochloa crus galli var. praticola Species 0.000 description 1
- 244000214240 Galinsoga parviflora Species 0.000 description 1
- 235000018914 Galinsoga parviflora Nutrition 0.000 description 1
- 241000209219 Hordeum Species 0.000 description 1
- 244000303225 Lamium amplexicaule Species 0.000 description 1
- 235000009198 Lamium amplexicaule Nutrition 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 241000205407 Polygonum Species 0.000 description 1
- 244000292697 Polygonum aviculare Species 0.000 description 1
- 235000006386 Polygonum aviculare Nutrition 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical class O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 241001148683 Zostera marina Species 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/26—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/56—Ring systems containing bridged rings
- C07C2603/58—Ring systems containing bridged rings containing three rings
- C07C2603/60—Ring systems containing bridged rings containing three rings containing at least one ring with less than six members
- C07C2603/66—Ring systems containing bridged rings containing three rings containing at least one ring with less than six members containing five-membered rings
- C07C2603/68—Dicyclopentadienes; Hydrogenated dicyclopentadienes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US426664A US3365289A (en) | 1964-01-24 | N - (1- or 2 - (4,5,6,7,8,9 - hexahydro - 4,7 - methanoindanyl)) - n',n' - dimethyl urea and use in weed control | |
| NL131870D NL131870C (US20110009641A1-20110113-C00256.png) | 1964-01-24 | ||
| DEB75134A DE1200062B (de) | 1964-01-24 | 1964-01-24 | Herbizid |
| BE658639D BE658639A (US20110009641A1-20110113-C00256.png) | 1964-01-24 | 1965-01-21 | |
| GB2868/65A GB1086527A (en) | 1964-01-24 | 1965-01-22 | Urea derivatives and mixtures containing them |
| FR2929A FR1434223A (fr) | 1964-01-24 | 1965-01-22 | Agents destinés à empêcher la croissance de plantes indésirables |
| DK37265AA DK117748B (da) | 1964-01-24 | 1965-01-22 | Middel til udryddelse af uønsket plantevækst. |
| NL6500853A NL6500853A (US20110009641A1-20110113-C00256.png) | 1964-01-24 | 1965-01-22 | |
| AT55265A AT255202B (de) | 1964-01-24 | 1965-01-22 | Mittel zur Bekämpfung von unerwünschtem Pflanzenwuchs |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB75134A DE1200062B (de) | 1964-01-24 | 1964-01-24 | Herbizid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1200062B true DE1200062B (de) | 1965-09-02 |
Family
ID=6978536
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEB75134A Pending DE1200062B (de) | 1964-01-24 | 1964-01-24 | Herbizid |
Country Status (7)
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1300559B (de) * | 1967-10-18 | 1969-08-07 | Basf Ag | N-[Hexahydro-4, 7-methanoindanyl]-N'-dimethyl-thioharnstoffe |
| DE1925199B1 (de) * | 1969-05-17 | 1971-03-25 | Basf Ag | Verfahren zur Herstellung von Tetrahydrodicyclopentadienyl-1-amin und Tetrahydrodicyclopentadienyl-2-amin durch Umsetzen von Dihydrodicyclopentadien mit Blausaeure und Schwefelsaeure und anschliessendes Verseifen der entstandenen Formamide |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH473537A (de) * | 1966-12-22 | 1969-06-15 | Geigy Ag J R | Herbizides Mittel |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3276855A (en) * | 1962-01-04 | 1966-10-04 | Velsicol Chemical Corp | N-alkylmercapto-ureas and a method for controlling weeds |
-
0
- NL NL131870D patent/NL131870C/xx active
- US US426664A patent/US3365289A/en not_active Expired - Lifetime
-
1964
- 1964-01-24 DE DEB75134A patent/DE1200062B/de active Pending
-
1965
- 1965-01-21 BE BE658639D patent/BE658639A/xx unknown
- 1965-01-22 AT AT55265A patent/AT255202B/de active
- 1965-01-22 NL NL6500853A patent/NL6500853A/xx unknown
- 1965-01-22 DK DK37265AA patent/DK117748B/da unknown
- 1965-01-22 GB GB2868/65A patent/GB1086527A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1300559B (de) * | 1967-10-18 | 1969-08-07 | Basf Ag | N-[Hexahydro-4, 7-methanoindanyl]-N'-dimethyl-thioharnstoffe |
| DE1925199B1 (de) * | 1969-05-17 | 1971-03-25 | Basf Ag | Verfahren zur Herstellung von Tetrahydrodicyclopentadienyl-1-amin und Tetrahydrodicyclopentadienyl-2-amin durch Umsetzen von Dihydrodicyclopentadien mit Blausaeure und Schwefelsaeure und anschliessendes Verseifen der entstandenen Formamide |
Also Published As
| Publication number | Publication date |
|---|---|
| AT255202B (de) | 1967-06-26 |
| GB1086527A (en) | 1967-10-11 |
| US3365289A (en) | 1968-01-23 |
| BE658639A (US20110009641A1-20110113-C00256.png) | 1965-07-22 |
| NL131870C (US20110009641A1-20110113-C00256.png) | |
| NL6500853A (US20110009641A1-20110113-C00256.png) | 1965-07-26 |
| DK117748B (da) | 1970-05-25 |
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