DE1793756C3 - - Google Patents
Info
- Publication number
- DE1793756C3 DE1793756C3 DE19681793756 DE1793756A DE1793756C3 DE 1793756 C3 DE1793756 C3 DE 1793756C3 DE 19681793756 DE19681793756 DE 19681793756 DE 1793756 A DE1793756 A DE 1793756A DE 1793756 C3 DE1793756 C3 DE 1793756C3
- Authority
- DE
- Germany
- Prior art keywords
- methyl
- carbamate
- phenyl
- carbamoyloxy
- methylphenyl
- 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.)
- Expired
Links
Classifications
-
- 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
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)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verbin dungConnect manure
Melhyl-N-(3-(N'-hulyl-Melhyl-N- (3- (N'-hulyl-
N'-(3'-mcth>lphenyl)-carh-N '- (3'-mcth> lphenyl) -carh-
anu>yloxy)-phcnyl)-carbanialanu> yloxy) -phynyl) -carbanial
F. 105 106 CF. 105 106 C
Die bisher nicht bekannte Verbindung kann beispielsweise durch Umsetzung von entsprechenden N-Hydroxyphcnylurcthancii mit entsprechenden Isocyanaten oder Caibaniidsäurechloriden in au sich bekannter Weise hergestellt werden.The previously unknown compound can, for example, by implementing appropriate N-Hydroxyphcnylurcthancii with corresponding isocyanates or caibaniidic acid chlorides per se be produced in a known manner.
I )ie eiTniduugsgenuiße Verbindung kann allein oder .ils Mischung mit anderen Herbiziden und/oderI) The enjoyable connection can be used alone or .ils Mixture with other herbicides and / or
sonstigen Stoffen, zum Beispiel Düngemitteln, angewandt werden.other substances, e.g. fertilizers, applied will.
Die Anwendung der erfindungsgemäßen Verbindung erfolgt zweckmäßig in einer für eine Unkraut-Ί bekänipfung üblichen Weise in Form von Zubereitungen, wie zum Beispiel Pulvern, Streumittel. Granulaten, Lösungen, Emulsionen oder Suspensionen, unter Zusatz von flüssigen und/oder festen Trägersloffen beziehungsweise Verdünnungsmitteln in und gegebenenfalls von Netz-, Haft-, Emulgier- und/ oder Dispergierhilfsmitleln.The compound according to the invention is expediently used in a weed Ί the usual way in the form of preparations, such as powders, grit. Granules, solutions, emulsions or suspensions, with the addition of liquid and / or solid carriers or diluents in and, if necessary, of wetting, adhesive, emulsifying and / or dispersing aids.
Die Herstellung der verschiedenen Zuberei'ungsformen erfolgt in an sich bekannter Art und Weise, zum Beispiel durch Mahl- beziehungsweise Mischi" > verfahren.The production of the various forms of preparation takes place in a manner known per se, for example by grinding or mixing " > proceed.
Zur selektiven Unkraulbekämpfung haben sich zum Teil schon Aufwandmengen von etwa 0,3 kg Wirksubstunz/hu an als ausreichend erwiesen.For selective weed control, in some cases, application rates of around 0.3 kg of active substance / hu have been found proved to be sufficient.
Die herbizide Wirkung der erlindungsgemäßen Ver- -'» bindung geht aus den folgenden Versuchsbeispiden hervor.The herbicidal effect of the compound according to the invention is based on the following experimental examples emerged.
_'"> Im Gewächshausversueh wurden die in der Tabelle aufgerührten Pllanzenarten im Nachauflaufverfahren mit der erfindungsgemäßen Verbindung_ '"> In the greenhouse experiment the in the table listed plant species in the post-emergence process with the compound according to the invention
(1) Melhyl-N-(3-(N'-n-bulyl-N'-(3'-meth\l-phenyl)-earbanioyloxy)-phenyl)-carbamat (1) Methyl-N- (3- (N'-n-bulyl-N '- (3'-meth \ l-phenyl) -earbanioyloxy) -phenyl) -carbamate
sowie den Vergleichsmilldnas well as the comparative mill
(2) Melhyl-N-(3-(N'-(3'-melhylphenyl)-carbamoylo\y)-phenyl)-carbamat (2) Methyl-N- (3- (N '- (3'-methylphenyl) -carbamoylo \ y) -phenyl) -carbamate
(3) lsopropyl-N-(3-chlorphcnyl)-carbamat(3) Isopropyl N- (3-chlorophynyl) carbamate
!l (4) Melh\l-N-(3-melhylcarbamoylo\yphenyl|- ! l (4) Melh \ lN- (3-methylcarbamoylo \ yphenyl | -
carbamat
(5) Methyl-N-methyl-N-(3-(N'-melh)l-carbamate
(5) methyl-N-methyl-N- (3- (N'-melh) l-
N-(.V-niethylphenyl)-carbanioylo\y |-phenyl)-carbamat N - (. V-niethylphenyl) -carbanioylo (y | -phenyl) -carbamate
in einer Aufwandmenge von 3 kg Wirkstoff ha behandelt. treated at an application rate of 3 kg of active ingredient ha.
Die Mittel wurden als Emulsionen in 500 liter Wasser je Hektar ausgebracht. Zwei Wochen nachThe agents were applied as emulsions in 500 liters of water per hectare. Two weeks after
Γι der Behandlung erfolgte die Auswertung durch Boiiiturentsprecheiul einer Bewertungsskiila von I) »total vernichtet« bis IO = »nicht geschädigt«.After the treatment, the evaluation was carried out by Boiiiturentsprecheiul an evaluation skiila from I) "totally destroyed" to IO = "not damaged".
Die erhaltenen Befunde /eigen deutlich die wesentlich bessere Selektivität der eriiiuiiingsgeniiißeu Ver-The results obtained clearly show the significantly better selectivity of the
i(i bindung gegenüber den wichtigen Kultiupllaii/en Mais, Weizen und Geiste bei ausgezeichneter Unkiaulwiikuim im Vergleich /u den bekaiinlen Mitteln.i (i bond to the important cultural sites Corn, wheat and spirits with excellent Unkiaulwiikuim in comparison to the known means.
Fortsetzung 3
continuation
0
00
0
0
IO
υ IO
IO
υ
K)
10K)
K)
10
Polygonum lapathi-
folium
C'hrysanthemus
segetum
0 = total vernichtet.
10 = nicht geschädigt. Ipomoea purpurea
Polygonum lapathi-
folium
C'hrysanthemus
segetum
0 = totally destroyed.
10 = not damaged.
0 I 4
1 8 100 2 7
0 I 4
1 8 10
Im Gewächshausversueh wurden dl·", in der Tabelle aufgeführten Pllan/enarten im Nachaiiflaufverfahreii mit der erfindungsgemäßen VerbindungIn Gewächshausversueh dl · "were in the table listed Plélan / enarten in Nachaiiflaufverfahreii with inventive compound
(I) Methyl-N-(3-(N'-n-bulyI-N'-(.V-meth)lphen>l)-carbamoyloxy)-phenyl)-carbamat (I) methyl N- [3- (N'-n-bulyI-N '- (. V-meth) lphen> l) -carbamoyloxy) -phenyl) -carbamate
sowie dem Vergleichsmittelas well as the comparison means
(6) \lelhyl-N-(3-<N'-(3-lluorphen>l)-carbamo>loxy)-phen >l)-carbamat(6) \ lethyl-N- (3- <N '- (3-fluorophen> l) -carbamo> loxy) -phen > l) carbamate
in einer Aufwandmenge von 3 kg Wirkstoff ha behandelt. treated at an application rate of 3 kg of active ingredient ha.
Die Mittel wurden als Emulsionen in 500 Liter Wasser je Hektar ausgebracht. Zwei Wochen nach der Uehandlung erfolgte die Auswertung durch Bonitur entsprechend einer Bewerlungsskala von 0 - »total vernichtet« bis 10 = »nicht geschädigt«.The agents were applied as emulsions in 500 liters of water per hectare. Two weeks after the The evaluation was carried out by means of a rating according to a rating scale from 0 - "totally destroyed" to 10 = "not damaged".
Die erhaltenen Befunde /eigen deutlich die wesentlich bessere Selektivität der erfind ungsgenüilten Verbindung gegenüber Baumwolle bei hervorragender herbi/ider Wirkung gegen Amarantus r. und andere Unkräuter im Veruleich/ti der bekannten VerbindungThe findings obtained clearly show the significantly better selectivity of the compound in accordance with the invention compared to cotton with excellent herbicidal action against Amarantus r. and other Weeds in the Veruleich / ti the known connection
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19681793756 DE1793756B2 (en) | 1968-06-20 | 1968-06-20 | DIURETHANE |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19681793756 DE1793756B2 (en) | 1968-06-20 | 1968-06-20 | DIURETHANE |
Publications (3)
Publication Number | Publication Date |
---|---|
DE1793756A1 DE1793756A1 (en) | 1973-05-24 |
DE1793756B2 DE1793756B2 (en) | 1976-12-16 |
DE1793756C3 true DE1793756C3 (en) | 1978-05-18 |
Family
ID=5707796
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19681793756 Granted DE1793756B2 (en) | 1968-06-20 | 1968-06-20 | DIURETHANE |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE1793756B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2413933A1 (en) * | 1974-03-20 | 1975-09-25 | Schering Ag | DIURETHANE WITH SELECTIVE HERBICIDAL EFFECT |
-
1968
- 1968-06-20 DE DE19681793756 patent/DE1793756B2/en active Granted
Also Published As
Publication number | Publication date |
---|---|
DE1793756A1 (en) | 1973-05-24 |
DE1793756B2 (en) | 1976-12-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE1218793B (en) | Selective herbicidal agents | |
DE1284151B (en) | Selective herbicides | |
DE1620448C3 (en) | Urea or thiourea derivatives of 3-methylisothiazole | |
DE2108975C3 (en) | N-acyl diurethanes and herbicidal agents containing them | |
DE1793756C3 (en) | ||
DE1642346C3 (en) | Herbicidal agents | |
DE69331164T2 (en) | Phytosanitary products containing an oxynil and at least one compound that is liquid at ambient temperature and process for their use | |
DE2121957C3 (en) | Diurethanes and herbicidal compositions containing them | |
DE1793755C3 (en) | Diurethanes and herbicidal compositions containing them | |
DE2020729C2 (en) | Herbicidal agents based on N- (3- (N'-aryl-carbamoyloxy) -phenyl) -carbamates | |
DE1242936B (en) | Selective herbicides | |
DE1793751C3 (en) | Diurethanes and herbicidal compositions containing them | |
DE2404659C2 (en) | Selectively herbicidal mixture of active ingredients for post-treatment of cereal crops | |
DE1542889B2 (en) | Agent for combating weeds based on phenylurea Hoechst AG, 6000 Frankfurt | |
DE1938612C3 (en) | Biscarbamates and herbicidal agents | |
DE1567165C3 (en) | Carbamate-based algicidal agents | |
DE1793753C3 (en) | Diurethanes and herbicidal compositions containing them | |
DE1793755B2 (en) | DIURETHANES AND HERBICIDALS CONTAINING THESE AGENTS | |
DE1793752C3 (en) | Diurethanes and herbicidal compositions containing them | |
AT275233B (en) | Weed control means | |
AT307439B (en) | Process for the production of new urea or thiourea derivatives | |
DE1793751B2 (en) | Diurethanes and herbicidal compositions containing them | |
DE1255983B (en) | Preparations for influencing plant growth | |
DE2843691A1 (en) | DIURETHANE, METHOD FOR PRODUCING THESE COMPOUNDS AND THE SELECTIVE HERBICIDES CONTAINING THEM | |
DE2121958C3 (en) | Herbicidal agents based on carbamoyloxyphenyl carbamate mixtures |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C3 | Grant after two publication steps (3rd publication) |