SU578819A3 - Herbicide - Google Patents

Herbicide

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Publication number
SU578819A3
SU578819A3 SU7201738083A SU1738083A SU578819A3 SU 578819 A3 SU578819 A3 SU 578819A3 SU 7201738083 A SU7201738083 A SU 7201738083A SU 1738083 A SU1738083 A SU 1738083A SU 578819 A3 SU578819 A3 SU 578819A3
Authority
SU
USSR - Soviet Union
Prior art keywords
plants
treatment
emergence
results
methyl
Prior art date
Application number
SU7201738083A
Other languages
Russian (ru)
Inventor
Рор Отто
Original Assignee
Циба-Гейги 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 Циба-Гейги Аг (Фирма) filed Critical Циба-Гейги Аг (Фирма)
Application granted granted Critical
Publication of SU578819A3 publication Critical patent/SU578819A3/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D203/00Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D203/04Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D203/06Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D203/16Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with acylated ring nitrogen atoms
    • C07D203/20Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with acylated ring nitrogen atoms by carbonic acid, or by sulfur or nitrogen analogues thereof, e.g. carbamates
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/28Derivatives 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 six-membered aromatic rings of a carbon skeleton
    • C07C275/30Derivatives 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 six-membered aromatic rings of a carbon skeleton being further substituted by halogen atoms, or by nitro or nitroso groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/64Derivatives 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 singly-bound to oxygen atoms

Description

(54) ГЕРБИЦИДНОЕ СРЕДСТВО(54) HERBICID MEANS

где R - водород или метил;where R is hydrogen or methyl;

R - метил или метоксигрунпа; X - кислород или сера.R is methyl or methoxygruppa; X - oxygen or sulfur.

Средство согласно изобретению эффективно поражает нежелательные растени  как при предвсходовом , так и послевсходовом применении. Реко The agent according to the invention effectively affects undesirable plants in both pre-emergence and post-emergence applications. Reko

мендуемые дозы этих делей от 0,1 до 10 кг/га, предпочтительно от 0,5 до 5 кг/га. The recommended doses of these drugs are from 0.1 to 10 kg / ha, preferably from 0.5 to 5 kg / ha.

Формы применени  предлагаемого соединени  обычные: растворы эмульсии, суспензии, пастц, порошки и т.д. Их готов т известны ™ способами.The form of application of the proposed compound is common: emulsion solutions, suspensions, pasty, powders, etc. They are prepared in known ™ ways.

Содержание действующих веществ в этих формах от 0,1 до 95 вес.%.The content of active substances in these forms is from 0.1 to 95 wt.%.

Окюоб получени  данных соединений основан на реакции 3 трифторметил - 4 фторфенилизоцианата или йзотиоцианата с соответствующими аминами . Их можно получать также из 3 - трифторметил - 4 - фтораиилина и соответствующих изонианатов или карбамоилхлоридов.The preparation of these compounds is based on the reaction of 3 trifluoromethyl - 4 fluorophenyl isocyanate or isosothiocyanate with the corresponding amines. They can also be prepared from 3-trifluoromethyl-4-fluoroiiline and the corresponding isoniachates or carbamoyl chlorides.

Соединени  указанной обшей формулы:Compounds of the above general formula:

N - 3 - трифторметил - 4 - фторфенил - N , NN - 3 - trifluoromethyl - 4 - fluorophenyl - N, N

-диметилмочевина (1)-dimethylurea (1)

N - 3 - трифторметил - 4 - фторфенил - Ы -метил - N - метоксимочевина (II)N - 3 - trifluoromethyl - 4 - fluorophenyl - S-methyl - N - methoxyurea (II)

N - 3 - трифторметил - 4 - фторфенил - N -метилмочевина (III)N - 3 - trifluoromethyl - 4 - fluorophenyl - N-methyl urea (III)

N 3 - трифторфенил - 4 - фторфенил - N,N-диметилмочевина (IV)N 3 - trifluorophenyl - 4 - fluorophenyl - N, N-dimethylurea (IV)

Пример 1. В услови х теплины высевают следующие активные растени : овсюг, щетинник, горчицу и клоповник.Example 1. Under the conditions of the greenhouse, the following active plants are sown: wild oats, bristles, mustard, and black rats.

Послевсходовую обработку данных растений провод т 1%-ным водным раствором соединений, и II через 10-12 дней после посева на стадии 2-3 ;шстьев. Определение действи  веществ производ т через 30 суток после обработки растений. Предвсходовую обработку растеюш осуществл ют через 24ч после посева растений. Г зультаты обработки соединений I и II показаны в табл. 1 и 2 соответственно.The post-emergence treatment of these plants was carried out with a 1% aqueous solution of the compounds, and II 10–12 days after sowing at stage 2-3; The determination of the effect of the substances was made 30 days after the treatment of the plants. Pre-emergence treatment is done 24 hours after sowing the plants. The results of the treatment of compounds I and II are shown in Table. 1 and 2 respectively.

Результаты оценивают в примерах 1 и 2 по следующей шкале: 1-3- растени  не повреждены или едва повреждены; 4-6- средн   степень поврежде1ш ; 7-8 - т желые повреждени ; 9 растени  погибли.The results are evaluated in examples 1 and 2 according to the following scale: 1-3 plants are intact or barely damaged; 4-6 is the average degree of damage; 7-8 - severe damage; 9 plants died.

Таблица 1Table 1

РастениеPlant

Пример 2. В услови х теплицы вь севают опытные растени  и провод т предвсходовые и послевсходовые опыты.Example 2. Under greenhouse conditions, experimental plants were sown and pre-emergence and post-emergence experiments were carried out.

при послевсходрвой обработке растени  обрабатьтают через 10-12 дней после посева на стадии 2-3 листьев. Обработку ведут 1%-ным воднымduring post-harvest treatment, plants are thawed 10-12 days after sowing at the 2-3 leaf stage. Processing lead 1% water

Таблица 3Table 3

ОбработкаTreatment

раствором; доза 2 кг/га по действующему веществу . Оценку результатов провод т через 20 суток после обработки растений.solution; dose of 2 kg / ha for the active substance. The evaluation of the results was carried out 20 days after the treatment of the plants.

Предвсходовую обработку осуществл ют через 24ч после посева растений также 1%-ным водным раствором в дозе 2 кт/га.Pre-emergence treatment is carried out 24 hours after seeding the plants with a 1% aqueous solution at a dose of 2 kt / ha.

Результаты опытов представлены в табл. 3.The results of the experiments are presented in table. 3

Таблица 3Table 3

Пример 3. Дл  испытаний семена растений высевают в горшки с землей так, чтобы в каждом горшке могло развиватьс  по 8-20 растений. Горш ки помещают в теплицу.Example 3. For testing, plant seeds are sown in pots with soil so that 8-20 plants can develop in each pot. The pots are placed in the greenhouse.

Ир предвсходовой обработке землю в горшке опрыскивают заданным количеством испытываемого вещества на следующий день после высевани . Соединение в виде порошка раствор ют в воде. Кэдачество распыл емого раствора соответствует 4,1 и 0,5 кг/га. Растени  выращивают в тешшце при 22-23° С к 50-70% относит..льной влажности.Ir pre-harvest cultivation of the potted soil is sprayed with a predetermined amount of the test substance on the day after sowing. The powder is dissolved in water. The quality of the sprayed solution corresponds to 4.1 and 0.5 kg / ha. Plants are grown in tesh at 22-23 ° C to 50-70% relative humidity.

При послевсходовой обработке горшки, в которых бьши посе ны семена, помещают в теплицу.During post-harvest processing, pots in which seeds were planted are placed in a greenhouse.

Через 12 дней после посева на стадии 2-3 листьев, провод т опрыскивание их составом. Оценку результатов провод т через 4 недели после обработки по следующей шкале: 9 - растени  не повреждены, развиваютс  так же, как и растени  в контрольном опыте; 5 - 50% растений повреждено; I - растени  уничтожены. Результаты предвсходовой обработки приведены в табл. 4, а послевсходовой - в табл. 5. Дл  сравнени  использовали: N - 3 - трифторметилфенил - N ,N - диметилмочевину (А) ; - N - 3 - трифторметилфенил - N .метил- N - метоксимочевину (Б); N-3 .трифторметилфенил - N - метилмочевину (В).12 days after sowing at the stage of 2-3 leaves, they are sprayed with the composition. Evaluation of the results was carried out 4 weeks after the treatment according to the following scale: 9 - the plants are intact, develop in the same way as the plants in the control experiment; 5 - 50% of plants are damaged; I - plants destroyed. The results of pre-emergence processing are given in table. 4, and post-harvest - in table. 5. For comparison, N-3-trifluoromethylphenyl-N, N-dimethylurea (A) was used; - N - 3 - trifluoromethylphenyl - N .methyl- N - methoxyurea (B); N-3. Trifluoromethylphenyl - N - methyl urea (B).

Таблица 4Table 4

Таблица 5Table 5

Claims (2)

1. Патент Швейвдрии N« 478523, кл. А01 N 9/20,1969.1. Patent Shveyvdrii N "478523, cl. A01 N 9/20,1969. 2. Патент «РГ N 1284151, кл. 45 I 19/02, 1968.2. Patent «РГ N 1284151, cl. 45 I 19/02, 1968.
SU7201738083A 1970-02-02 1972-01-17 Herbicide SU578819A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH143070A CH533421A (en) 1970-02-02 1970-02-02 Biocidal agent

Publications (1)

Publication Number Publication Date
SU578819A3 true SU578819A3 (en) 1977-10-30

Family

ID=4210275

Family Applications (1)

Application Number Title Priority Date Filing Date
SU7201738083A SU578819A3 (en) 1970-02-02 1972-01-17 Herbicide

Country Status (9)

Country Link
BE (1) BE762357A (en)
BG (1) BG19138A3 (en)
CH (1) CH533421A (en)
DE (1) DE2103388C3 (en)
FR (1) FR2076917A5 (en)
GB (1) GB1326481A (en)
IL (1) IL36057A (en)
NL (1) NL7101317A (en)
SU (1) SU578819A3 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1473105A (en) * 1973-08-10 1977-05-11
GB2122901A (en) * 1982-05-21 1984-01-25 Sandoz Ltd Synergistic herbicidal mixture
KR20080086502A (en) * 2005-12-13 2008-09-25 아르피다 아게 Diphenyl urea derivatives
WO2017036405A1 (en) * 2015-09-02 2017-03-09 陈昆锋 Compound having protein tyrosine phosphatase shp-1 agonist activity

Also Published As

Publication number Publication date
DE2103388A1 (en) 1971-08-19
FR2076917A5 (en) 1971-10-15
GB1326481A (en) 1973-08-15
DE2103388B2 (en) 1979-05-31
BG19138A3 (en) 1975-04-30
CH533421A (en) 1973-02-15
DE2103388C3 (en) 1980-02-07
NL7101317A (en) 1971-08-04
IL36057A (en) 1974-07-31
BE762357A (en) 1971-08-02
IL36057A0 (en) 1971-03-24

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