SU528019A3 - Herbicide - Google Patents

Herbicide

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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
Application number
SU2005475A
Other languages
Russian (ru)
Inventor
Борошевски Герхард
Арндт Фридрих
Original Assignee
Шеринг Аг (Фирма)
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Шеринг Аг (Фирма) filed Critical Шеринг Аг (Фирма)
Application granted granted Critical
Publication of SU528019A3 publication Critical patent/SU528019A3/en

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N47/00Biocides, 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
    • A01N47/08Biocides, 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
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/12Carbamic 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
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N25/00Biocides, 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
    • A01N25/02Biocides, 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
    • A01N25/04Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N37/00Biocides, 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
    • A01N37/18Biocides, 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
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/541,3-Diazines; Hydrogenated 1,3-diazines
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N47/00Biocides, 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
    • A01N47/08Biocides, 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
    • A01N47/10Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/20N-Aryl derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N47/00Biocides, 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
    • A01N47/08Biocides, 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
    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/30Derivatives 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)

10 10 10 10 10 Пример 3. В оранжерее тест-растени  на ранней стадии развити  обрызгивают водной эмульсией гербициднога федства в дозе 2 кг/га при норме расхода 500 л/га. Через 14 дней определ ют rep&amp;iцидную активность, как в примере 1. Соеднне(ш  № 1, № 28-33 полностью уничтожают щирицу, дурниишик и портулак. Соединени  N1, № 28, N 30-33 полностью уничтожают щетинник. Дл  соединений № 28-31 гер&amp;1щщна  активность по отнощению к чешуехвостику и элевзине составл ет 0,5, 1, 0,5, 1 и 2, 4, 1, 1 балл соответственно . Гербицидна  активность соединени  № 29 по отношению к щетиннику равна 6 баллам. Формула изобретени  Гербииидное средство, содержащее действующее вещество и вспомогательиые компоненты, отичающеес  тем, что, с целью усилени  гербиидной активности и упучшеик  избирательности ействи , в качестве действующего вещества вз ты рилдиуретаны общей формулы 0-CO-NP P NH-CO-XR где R - аллил, алкил или галоидапкил с 1-4 атомами углерода; R - аллил, алкил, галоидалкил с 1-4 атомами углерода, циклогексил, бензил или фенилзтил; R - метил или этил; X - кислород или сера, вводимые в количестве вес. %.10 10 10 10 10 Example 3. In the greenhouse, test plants at an early stage of development are sprinkled with an aqueous emulsion of a herbicide formulation at a dose of 2 kg / ha at a consumption rate of 500 l / ha. After 14 days, the rep & acid activity was determined as in Example 1. Compound (W No. 1, No. 28-33 completely destroy shirrita, durniiishik and purslane. Compounds No. 1, No. 28, N 30-33 completely destroy the bristle. For connections No. 28-31 ger &amp; 1Hs activity with respect to scales and Elevzine is 0.5, 1, 0.5, 1 and 2, 4, 1, 1 points, respectively. Herbicidal activity of compound No. 29 with respect to bristles is 6 points. Claims of Invention. A herbicidal agent containing an active substance and auxiliary components, which is indicated by the fact that, in order to strengthen no herbicidal activity and the improvement of the selectivity of the action, as an active ingredient, take rildiurethanes of the general formula 0-CO-NP P NH-CO-XR where R is allyl, alkyl or haloalkyl with 1-4 carbon atoms; R is allyl, alkyl, haloalkyl with 1-4 carbon atoms, cyclohexyl, benzyl or phenylstil; R is methyl or ethyl; X is oxygen or sulfur, introduced in the amount of wt.%.
SU2005475A 1973-03-01 1974-02-28 Herbicide SU528019A3 (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

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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