SU528019A3 - Herbicide - Google Patents
HerbicideInfo
- Publication number
- SU528019A3 SU528019A3 SU2005475A SU2005475A SU528019A3 SU 528019 A3 SU528019 A3 SU 528019A3 SU 2005475 A SU2005475 A SU 2005475A SU 2005475 A SU2005475 A SU 2005475A SU 528019 A3 SU528019 A3 SU 528019A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- activity
- herbicidal
- allyl
- alkyl
- carbon atoms
- Prior art date
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
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- 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
- A01N47/20—N-Aryl derivatives thereof
-
- 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Toxicology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
ГЕРБИЦИДНОЕ СРЕДСТВОHERBICIDE MEANS
Изобретение относитс к химическим средствам борьбь: с сорной растительностью в посевах воздельтаемых культур. Известно гербицндное средство, содержащее действующее вещество; например производные карб аминовой кислоты, и вспомогательные компоненты .. Однако известное гербидадное средство недостаточно избирательно, например по отноше1шю к хлопчатнику. Цель изобрете ш - усилерше гербицийной активности и повыщение избирательности де««сви достигаетс тем, что в качестве действуттцего вещества вз ты арилдиуретаны общей фориуль: O-CO-NR T NH-CO-XTr где R - аллил, алкил илн галоИудакил с 1-4 атомами углерода; R - аллил, алкил, галоидалки1 с 1-4 атомами углерода, циклогексил, ли фенилэтил ; R - метил или этил; X - кисло юд или сера, которые ввод т в гербицидное qieucrso в количестве 1О-80 вес.%. Формы применени гербиин ного средства обычные: растворы, эмульсии, пасты, порощки, приготавливаемые общеизвестными способами. Доза применени 1-3 кт/rs (везде по действую щемх ществу). В дозе по 10 кг/га гербицид}(О( средство сохран ет и збнрательность действи . Предпагаемре гербицидное средство эффективно при довсходовом и особенно при послевсходовом применении. Преллагаемые арилдиуретаны получают при взаимодействии 3 -оксиарилкарбаматов или тиокарбаматов-с кapбaмoилxлopидa ffl, при взаимодействии 3 - хлоркарбоиилоксифсни.чкарбаматов или тиокарбаматов с соответствуюишш аминами или при воссга11овле1ши 3 - нитрофенилкарбаматов до аминов с пос.челующим взаимодейств ем с хлоркарбонатами или тиокарбонатами. В табл. 1 приведены арил/шуретаиы указанной формулы, ис-пьианные в качестве действующего вещества, вводимого в состав гербмии иого средства .This invention relates to chemical control agents: weeds in crops of cultivated crops. Known herbicidal agent containing the active substance; for example, derivatives of carboamic acid, and auxiliary components .. However, the well-known herbicidal agent is not selective enough, for example, in relation to cotton. The purpose of the invention is to increase the herbicide activity and increase the selectivity of de "св св достигает достигает by the fact that aryl diurethanes of common foriul are taken as active substance: O-CO-NR T NH-CO-XTr where R is allyl, alkyl or halo Iudacyl with 1- 4 carbon atoms; R is allyl, alkyl, haloalkyl with 1-4 carbon atoms, cyclohexyl, or phenylethyl; R is methyl or ethyl; X is acidic or sulfur, which is introduced into the herbicidal qieucrso in an amount of 10-8% by weight. The forms of application of the herbicine agent are common: solutions, emulsions, pastes, powders prepared by well-known methods. Dose of 1-3 kt / rs (everywhere in the active substance). At a dose of 10 kg / ha, a herbicide} (O (the remedy also preserves the effectiveness of action. The herbicidal agent is pre-treated) is effective for pre-emergence and especially for post-emergence application. The proposed aryl diuretans are obtained by the interaction of 3-hydroxyaryl carbamates or thiocarbamates with carbamate chromium lipoproteins, the lipid lipids are obtained by the interaction of 3-hydroxyaryl carbamates or thiocarbamates with carpamoylchloridhloridhloridhloridhloridhloridhloridhloridrochloride. chlorocarboxyloxys.chcarbamates or thiocarbamates with the corresponding amines or in case of recovery of 3 3-nitrophenylcarbamate to amines with the desired interaction with chlorocarbonates or thiocarbonates. s aryl / shuretaiy said formula is-piannye as an active ingredient introduced into the composition gerbmii iogo means.
Эти соединени хорошо растворимы в ацетоне, шклогексаноне, уксусном эфире, изофоооне, Jфире и тетрагидрофуране и практически нерастворимы а воде и легком бензине.These compounds are readily soluble in acetone, shcohexanone, ethyl acetate, isofooone, Jfere, and tetrahydrofuran and are practically insoluble in water and light gasoline.
Наиболее избирательны по отношению к арахи ,. .1ркови и рису соединети;. 2. 14-17, 21, 23, 28,The most selective in relation to arahi,. .1 rkovi and rice connect ;. 2. 14-17, 21, 23, 28,
, : : 34.,:: 34.
Пример . Тест-растени в ранней стадии развити обрабатьшают в оранжерее эмульсией гербицчциого срсдсша в дозе 3 кг/га при расхода 500 л/га. Через 14 дней после чки определ ют гсрбишцу{ую активность л;:;:., ..: ч соединений по дес тибальной шкале: ..-(юлног уничтожеьше растений, 10- отсутствие :ичрсжд;:ни. Получе1шые результаты привсдень. в таб.: 1.An example. Test plants at an early stage of development are treated in a greenhouse with an emulsion of gerbic acid at a dose of 3 kg / ha at a flow rate of 500 l / ha. After 14 days after the test, the grsrbitsu {activity l;;:::., ..: h of compounds was determined according to the decimal scale: ..- (very few plants, 10 - no: ichrzhzhd:; not. The received results in the afternoon. tab .: 1.
Продолжение табл. 2Continued table. 2
Пример 2. В оранжерее тест- pacieimH перед всходом опрыскивают водными эмульси ми гербицидного средства в дозе 3 кг/га при норме расхо10 10 10 10 10 10 10 10 10 10Example 2. In a greenhouse, test-pacieimH before sprouting is sprayed with aqueous emulsions of a herbicidal agent at a dose of 3 kg / ha at a rate of 10 10 10 10 10 10 10 10 10 10
Продолжение табл.2Continuation of table 2
да 500 л/га. Через 14 дней после обработки определ ют гербицидную активность, как в примере 1. Результаты опытов приведены в табл. 3.yes 500 l / ha. 14 days after treatment, the herbicidal activity is determined as in Example 1. The results of the experiments are shown in Table. 3
Таблица 3Table 3
J О О ОJ o o o o
4 О4 o
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2310648A DE2310648C3 (en) | 1973-03-01 | 1973-03-01 | Diurethanes, processes for the preparation of these compounds and selective herbicidal agents containing them |
Publications (1)
Publication Number | Publication Date |
---|---|
SU528019A3 true SU528019A3 (en) | 1976-09-05 |
Family
ID=5873703
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU2005475A SU528019A3 (en) | 1973-03-01 | 1974-02-28 | Herbicide |
SU7402005371A SU578867A3 (en) | 1973-03-01 | 1974-02-28 | Method of preparing diuretan derivatives |
SU752130994A SU592352A3 (en) | 1973-03-01 | 1975-05-06 | Method of preparing diurethans |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU7402005371A SU578867A3 (en) | 1973-03-01 | 1974-02-28 | Method of preparing diuretan derivatives |
SU752130994A SU592352A3 (en) | 1973-03-01 | 1975-05-06 | Method of preparing diurethans |
Country Status (25)
Country | Link |
---|---|
JP (1) | JPS572681B2 (en) |
AT (1) | AT332163B (en) |
BE (1) | BE811783A (en) |
BG (2) | BG27894A4 (en) |
BR (1) | BR7401460D0 (en) |
CH (1) | CH586506A5 (en) |
CS (1) | CS172276B2 (en) |
DD (1) | DD112071A5 (en) |
DE (1) | DE2310648C3 (en) |
EG (1) | EG11202A (en) |
ES (1) | ES423651A1 (en) |
FR (1) | FR2219935B1 (en) |
GB (1) | GB1467513A (en) |
HK (1) | HK1978A (en) |
HU (1) | HU168694B (en) |
IL (1) | IL44276A (en) |
IT (1) | IT1049220B (en) |
MY (1) | MY7800110A (en) |
NL (1) | NL7402851A (en) |
PH (1) | PH12899A (en) |
PL (1) | PL89818B1 (en) |
RO (2) | RO69331A (en) |
SU (3) | SU528019A3 (en) |
YU (1) | YU39651B (en) |
ZA (1) | ZA741366B (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2557552C2 (en) * | 1975-12-18 | 1984-12-20 | Schering AG, 1000 Berlin und 4709 Bergkamen | Diurethanes and herbicidal agents containing these compounds as active ingredients |
JPS5833970B2 (en) * | 1978-09-08 | 1983-07-23 | 富士通株式会社 | Inter-processor communication method |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3404975A (en) * | 1964-12-18 | 1968-10-08 | Fmc Corp | m-(carbamoyloxy)-carbanilates as herbicides |
DE1593523A1 (en) * | 1966-10-15 | 1970-07-16 | Schering Ag | Process for the preparation of N-carbamoyloxyphenyl carbamates |
DE2109798C3 (en) * | 1971-02-23 | 1979-12-20 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | N-3-Carbamoyloxyphenyl-Thiolcarbamate and herbicidal agent containing them |
-
1973
- 1973-03-01 DE DE2310648A patent/DE2310648C3/en not_active Expired
-
1974
- 1974-02-18 YU YU404/74A patent/YU39651B/en unknown
- 1974-02-19 BG BG7433634A patent/BG27894A4/en unknown
- 1974-02-19 BG BG7425826A patent/BG27871A3/en unknown
- 1974-02-20 CS CS1255A patent/CS172276B2/cs unknown
- 1974-02-21 HU HUSC461A patent/HU168694B/hu unknown
- 1974-02-25 IL IL44276A patent/IL44276A/en unknown
- 1974-02-26 EG EG59/74A patent/EG11202A/en active
- 1974-02-26 ES ES423651A patent/ES423651A1/en not_active Expired
- 1974-02-26 GB GB862174A patent/GB1467513A/en not_active Expired
- 1974-02-27 RO RO7477844A patent/RO69331A/en unknown
- 1974-02-27 RO RO7487862A patent/RO69716A/en unknown
- 1974-02-27 PH PH15556A patent/PH12899A/en unknown
- 1974-02-27 FR FR7406607A patent/FR2219935B1/fr not_active Expired
- 1974-02-27 DD DD176840A patent/DD112071A5/xx unknown
- 1974-02-28 SU SU2005475A patent/SU528019A3/en active
- 1974-02-28 PL PL1974169153A patent/PL89818B1/pl unknown
- 1974-02-28 SU SU7402005371A patent/SU578867A3/en active
- 1974-02-28 BR BR1460/74A patent/BR7401460D0/en unknown
- 1974-02-28 JP JP2372174A patent/JPS572681B2/ja not_active Expired
- 1974-02-28 AT AT165674A patent/AT332163B/en not_active IP Right Cessation
- 1974-03-01 NL NL7402851A patent/NL7402851A/xx not_active Application Discontinuation
- 1974-03-01 BE BE141567A patent/BE811783A/en not_active IP Right Cessation
- 1974-03-01 CH CH294774A patent/CH586506A5/xx not_active IP Right Cessation
- 1974-03-01 ZA ZA00741366A patent/ZA741366B/en unknown
- 1974-04-08 IT IT20677/74A patent/IT1049220B/en active
-
1975
- 1975-05-06 SU SU752130994A patent/SU592352A3/en active
-
1978
- 1978-01-12 HK HK19/78A patent/HK1978A/en unknown
- 1978-12-30 MY MY110/78A patent/MY7800110A/en unknown
Also Published As
Publication number | Publication date |
---|---|
AT332163B (en) | 1976-09-10 |
YU39651B (en) | 1985-03-20 |
DE2310648C3 (en) | 1982-05-06 |
RO69716A (en) | 1981-05-30 |
IT1049220B (en) | 1981-01-20 |
BR7401460D0 (en) | 1974-10-29 |
ZA741366B (en) | 1975-01-29 |
AU6606774A (en) | 1975-08-28 |
DD112071A5 (en) | 1975-03-20 |
ATA165674A (en) | 1975-12-15 |
DE2310648B2 (en) | 1981-07-30 |
BG27871A3 (en) | 1980-01-15 |
RO69331A (en) | 1981-05-15 |
GB1467513A (en) | 1977-03-16 |
ES423651A1 (en) | 1976-04-16 |
JPS5040732A (en) | 1975-04-14 |
YU40474A (en) | 1982-05-31 |
PH12899A (en) | 1979-10-04 |
JPS572681B2 (en) | 1982-01-18 |
SU578867A3 (en) | 1977-10-30 |
DE2310648A1 (en) | 1974-09-19 |
HK1978A (en) | 1978-01-20 |
BG27894A4 (en) | 1980-01-15 |
FR2219935A1 (en) | 1974-09-27 |
MY7800110A (en) | 1978-12-31 |
CH586506A5 (en) | 1977-04-15 |
HU168694B (en) | 1976-06-28 |
NL7402851A (en) | 1974-09-03 |
EG11202A (en) | 1977-09-30 |
IL44276A (en) | 1977-10-31 |
IL44276A0 (en) | 1974-05-16 |
SU592352A3 (en) | 1978-02-05 |
PL89818B1 (en) | 1976-12-31 |
BE811783A (en) | 1974-09-02 |
CS172276B2 (en) | 1976-12-29 |
FR2219935B1 (en) | 1977-09-16 |
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