SU591123A3 - Herbicide - Google Patents

Herbicide

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Publication number
SU591123A3
SU591123A3 SU762393349A SU2393349A SU591123A3 SU 591123 A3 SU591123 A3 SU 591123A3 SU 762393349 A SU762393349 A SU 762393349A SU 2393349 A SU2393349 A SU 2393349A SU 591123 A3 SU591123 A3 SU 591123A3
Authority
SU
USSR - Soviet Union
Prior art keywords
alkyl
alkoxy
glycine
active principle
alkylamino
Prior art date
Application number
SU762393349A
Other languages
Russian (ru)
Inventor
Драбер Вильфрид
Дикоре Карльфрид
Тиммлер Гельмут
Ойе Лудвиг
Рудольф Шмидт Роберт
Original Assignee
Байер 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 Байер Аг (Фирма) filed Critical Байер Аг (Фирма)
Application granted granted Critical
Publication of SU591123A3 publication Critical patent/SU591123A3/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D253/00—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00
    • C07D253/02—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 not condensed with other rings
    • C07D253/06—1,2,4-Triazines
    • C07D253/065—1,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members
    • C07D253/07—1,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members with hetero atoms, or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D253/075—Two hetero atoms, in positions 3 and 5
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D253/00—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00
    • C07D253/02—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 not condensed with other rings
    • C07D253/06—1,2,4-Triazines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D253/00—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00
    • C07D253/02—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 not condensed with other rings
    • C07D253/06—1,2,4-Triazines
    • C07D253/065—1,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members
    • C07D253/07—1,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members with hetero atoms, or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Plural Heterocyclic Compounds (AREA)

Description

(54) ГЕРБИЦИДНОБ СРЕДСТВО(54) HERBICID MEANS

чало производные (1,2,4-триааин-5 -он- 1-45л)-глицина общей формулыChalo derivatives (1,2,4-triaain-5-one- 1-45l) -glycine of the general formula

ООВHlp

ift-coB ift-coB

R - апкил, алкокси-, алкилтио- илн алкиламиногрутаю;R is apkyl, alkoxy, alkylthioyl, alkylaminohexane;

Т - anKHLnj циклоалкил или незаме- щенн1 й или замещенный фенил;T is anKHLnj cycloalkyl or unsubstituted or substituted phenyl;

R - , алкил, алкенил или алкинвл;R -, alkyl, alkenyl or alkynvl;

11 - гицрокснльна , алкокси-е алкйлТИО- , амино-, алкиламино- или пиалкиламиногрупаа ,11 - gyroxyl, alkoxy-e alkylTHO-, amino-, alkylamino- or pylaminogroup,

а также добавку, выбранную из группы: растворитель, эмульгатор, циспергатор, причем весовое содержание действующего начала составл ет-от 0,1 до 95 вес.%,as well as an additive selected from the group of: solvent, emulsifier, cispergator, the weight content of the active principle being from 0.1 to 95% by weight,

В табл. 1 дана физико-химическа  ка« рактеристнка указанных соединений.In tab. 1 shows the physico-chemical characterization of these compounds.

При м е р 1. Растени  картофел  овсЛГа , щирицы и, мари белой высотой отExample 1. Potatoes of ovslg, shchiritsa, and mari white height from

.5 до 15. см обрабат ывают эталоном А 4-амино-6- рет-бутил- -нметилтио-1 ,2,4гТриазин-5-oBOMji а также соединением № 1- N -(3-метилтио-6- рет-бутил-1,2 4-триазин-в-он-4-ил )- ot -втокси и соединением Jvfe 7 - :N -(3-метилтно-в-тре1 -бутил-1 ,2,4-триази -5-он-4 -ил)- б(. -метокс в дозах 1,2 и 3 кг/га..5 to 15. cm are treated with the standard A 4-amino-6-ret-butyl-methyl-thio-1, 2.4 g Triazin-5-oBOMji and also with compound No. 1-N- (3-methylthio-6-ret-butyl -1,2 4-triazin-in-one-4-yl) - ot -voxy and compound Jvfe 7 -: N - (3-methyl-in-tre1 -butyl-1, 2,4-triazi -5-one -4 -il) - b (.-Methox at doses of 1.2 and 3 kg / ha.

Спуст  три недели провод т учет герби цдавой активности и избирательности действи  по 1ОО-бальной шкале: О - нет повреждений , ЮО - полна  гибель растений.Three weeks later, we take into account the herbic activity and selectivity of action according to the 1OO-point scale: O - no damage, SO - full of plant death.

Результаты испытаний представлены в табл.2.The test results are presented in table 2.

П р и м е р 2, Семена сои, кукурузы картофел , овсюга, куриного проса, росички кров ной, ширины, мари белой высевавэт влочву и спуст  24 ч обрабатывают почву этанолом А в дозах 0,625; Ij25; 2,S кг/га, а также соединени ми М 1, 7, 12„ 15   18 -31 в тех же дозах. Учет провод т через три недели по 1ОО-бальной шкале,PRI me R 2, Seeds of soybean, corn, potatoes, oats, chicken millet, rosicki of blood, breadth, Mari white seed, and 24 hours later, the soil is treated with ethanol A in doses of 0.625; Ij25; 2, S kg / ha, as well as compounds M 1, 7, 12 15 15 -31 in the same doses. Accounting is carried out after three weeks on a 1OO-scale,

Резулнгаты представлены в .Results are presented in

ПримеЕ 3, В почву высевают семена свеклыв галийсоти, ромашки, звездчатки, и, спуст  сутки, обрабатывают посевы в дозе 5 кг/га эталоном В - 4-амино-в-фенил-3-метилтио-1 ,2,4-триазин-5-оном и соединени ми № 4, 6 и 10, указанными в табл. 1.Example 3, the seeds are sown in the soil beet Galisot, chamomile, sprocket, and, after a day, treated crops in a dose of 5 kg / ha standard B - 4-amino-in-phenyl-3-methylthio-1, 2,4-triazine- 5th and the compounds nos. 4, 6, and 10 listed in Table. one.

Через три недели провод т учет герби- аидной активности по 1ОО - бальной After three weeks, an account is taken of the herbicidal activity of 1OO-ball

Результаты испытаний представлены в табл.4.The test results are presented in table 4.

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Claims (3)

«Q Формула изобретенк  Гербицвдное средство, включающее как действующее начало производные N -(1,2,4 -триазин-5-он-4-ил)-глицина, а также добавку , выбранную из группы: растворитель, эмульгатор, ййспергатор, отличают ш а   с   тем, что, с целью усилени  гер- бицидной активности и избирательности действи , оно сопержит в качестве произвоа ных ,N -(1,2,4- иазин-5-он-4-ил)-глицина соединение обшей формулы r-ira-CH-coH где - алкил алкокси-, алкилтиойлн алкиламиногруппа; 23 И алкил, пиклоалквл или незамещенный или замешенный феннл; Т - водорон, алкил, алкенил или алкинил; К - гидроксильна , алкокси-, алКИЛТИО- , амино-, алкиламино- или аиалкиламиногруппа , ,, причём весовое содержание действующего начала составл ет от 0,1 до 95 вес, %. Источники информации, прин тые во внимание при экспертизе; 1.Выложенна  за вка-ФРГ № 2224161, л. 45 S 19/О2, 1973. "Q The formula of the invention Herbaceous means, including as an active principle, derivatives of N - (1,2,4 -triazin-5-one-4-yl) -glycine, as well as an additive selected from the group: solvent, emulsifier, yspergator, are distinguished by and so that, in order to enhance the germicidal activity and selectivity of action, it will, as a derivative, N - (1,2,4-yazin-5-he-4-yl) -glycine, a compound of the general formula r- ira-CH-coH where is an alkyl alkoxy, alkylthioyl alkylamino group; 23 And alkyl, picloalkvl or unsubstituted or substituted fenl; T is voron, alkyl, alkenyl or quinil; K is a hydroxyl, alkoxy, alkylthio, amino, alkylamino, or alkylamino group, and the weight content of the active principle is from 0.1 to 95% by weight. Sources of information taken into account in the examination; 1. It is laid out for VKA-FRG No. 2224161, l. 45 S 19 / O2, 1973. 2.Патент Японии № 46-26357, О F 371, 1971 . 2. Japanese Patent No. 46-26357, O F 371, 1971. 3.Патент США № 3671523,кл. 71-25.3. US patent number 3671523, cl. 71-25.
SU762393349A 1975-09-13 1976-09-03 Herbicide SU591123A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19752540958 DE2540958A1 (en) 1975-09-13 1975-09-13 (1,2,4)-Triazinonyl glycine derivs. - useful as (selective) pre- or post-emergence herbicides

Publications (1)

Publication Number Publication Date
SU591123A3 true SU591123A3 (en) 1978-01-30

Family

ID=5956437

Family Applications (1)

Application Number Title Priority Date Filing Date
SU762393349A SU591123A3 (en) 1975-09-13 1976-09-03 Herbicide

Country Status (6)

Country Link
BE (1) BE846128A (en)
CS (1) CS193562B2 (en)
DE (1) DE2540958A1 (en)
PL (1) PL101377B1 (en)
SU (1) SU591123A3 (en)
ZA (1) ZA765431B (en)

Also Published As

Publication number Publication date
PL101377B1 (en) 1978-12-30
CS193562B2 (en) 1979-10-31
ZA765431B (en) 1977-08-31
DE2540958A1 (en) 1977-03-17
BE846128A (en) 1977-03-14

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