SU524493A3 - Herbicide - Google Patents

Herbicide

Info

Publication number
SU524493A3
SU524493A3 SU1415802A SU1415802A SU524493A3 SU 524493 A3 SU524493 A3 SU 524493A3 SU 1415802 A SU1415802 A SU 1415802A SU 1415802 A SU1415802 A SU 1415802A SU 524493 A3 SU524493 A3 SU 524493A3
Authority
SU
USSR - Soviet Union
Prior art keywords
alkyl
hydrogen
alkynyl
alkenyl
carbon atoms
Prior art date
Application number
SU1415802A
Other languages
Russian (ru)
Inventor
Лестер Хантер Дон
Джордж Вудс Уильям
Дуглас Стоун Джеймс
Райт Лефевр Сесил
Original Assignee
Юнайтед Стейтс Боракс Энд Кемикал Корпорейшн (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 Юнайтед Стейтс Боракс Энд Кемикал Корпорейшн (Фирма) filed Critical Юнайтед Стейтс Боракс Энд Кемикал Корпорейшн (Фирма)
Application granted granted Critical
Publication of SU524493A3 publication Critical patent/SU524493A3/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D203/00—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D203/04—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D203/06—Heterocyclic 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
    • C07D203/08—Heterocyclic 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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring nitrogen atom
    • C07D203/14—Heterocyclic 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 only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring nitrogen atom with carbocyclic rings directly attached to the ring nitrogen atom
    • 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
    • A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
    • A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
    • A01N33/18—Nitro compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/07—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms
    • C07C205/11—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to carbon atoms of six-membered aromatic rings
    • C07C205/12—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to carbon atoms of six-membered aromatic rings the six-membered aromatic ring or a condensed ring system containing that ring being substituted by halogen atoms

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Description

(54) ГЕРБИЦИД(54) HERBICID

-фенилендиамины, N , N -диэтил-2,4-динитpo-6-6poN - и N , М-пектиметилен-2,4-динитро-6-хлор-1 ,3 -фенилендиамины,-Phenylenediamine, N, N-diethyl-2,4-dinitpo-6-6poN - and N, M-pectimethylene-2,4-dinitro-6-chloro-1, 3-phenylenediamine,

Пример 1. Довсходова  обработка.Пример 2, Послевсходова  обраСемена тест-растений высевают в подго- gбогка,Example 1. Pre-emergence treatment. Example 2, Post-emergence seeds of test plants are sown in preparation,

товленную почву, обрабатывают соединени -Тест-растени  высотой 2,54 см обрабами № 1-3 в дозе 0,222 г/м и через 22тывают соединени ми № 1-3 в дозеsoil, the compounds of the Test Plant with a height of 2.54 cm are treated with the treatment No. 1-3 at a dose of 0.222 g / m and through the compound with the compound No. 1-3 at a dose

дн  после обработки определ ют гербицид-0,222 г/м и через 22 дн  после обработную активность по дев тибалльной шкале:ки провод т учет гербидидной активности,days after treatment, a herbicide of 0.222 g / m is determined, and 22 days after the treatment activity, a nine-point scale is used: the herbibid activity is taken into account,

О - отсутствие повреждений,Юкак в примере 1.O - no damage, Yukak in example 1.

5 - значительные повреждени  и гибельРезультаты опытов приведены в таблирастений в незначительной степени,це.5 - significant damage and death. The results of the experiments are given in the table of plants to a slight degree, cent.

9 - полна  гибель растений. Результаты опытов приведены в таблице.9 - full of death of plants. The results of the experiments are given in the table.

Claims (1)

Данные, .приведенные в таблице, свидетельствукут о высокой гербицидной активно ти и избирательности предлагаемых соединений , что особенно заметно при довсходовой обработке. Формула изобретени  Применение замещенных ароматических аминов общей формулы RtRj Ц где X - галоид или трифторметил; R - R.- водород, алкил, апкоксжапкил, алкенил, или алкинил, причем по крайней мере один из R - углеводородный радикал; Rj и R вместе с атомом азота и и R вместе с атомом азота могут образовьшать гегероцикл, содержащий ii-5 атомов углерода в цикле, в качестве гербици Приоритет по признакам: 01.О4.69 при X - трифгорметил, - водород, алкил, алкенил, алкинил R. - алкил, алкенил, алкинил или R. и R. и/или R и Rд вместе с атом азота могут образовывать гетероцикл, со держащий 2-5 атомов углерода в цикле. и R. 10 .11.69 при X - галоид, R водород; - Су. -апRJ и R - водород или С кил, причем по крайней мере один из R алкил , а R и R вместе содержат 3-5 атомов углерода. 10Д1,69 при X - трифгорметил; R R - водород, алкил, алкенил или алкинил , причем по крайней мере один из R - углеводородный радикал или R и R и/ /или R, и R вместе с атомом азота могут образовьшать гетероцикл, содержащий 2-5 атомов углерода в цикле.The data given in the table testify to the high herbicidal activity and selectivity of the proposed compounds, which is especially noticeable during the pre-emergence treatment. Claims of the invention Use of substituted aromatic amines of the general formula RtRj C where X is halogen or trifluoromethyl; R is R. is hydrogen, alkyl, apkoxjapkyl, alkenyl, or alkynyl, and at least one of R is a hydrocarbon radical; Rj and R together with the nitrogen atom and and R together with the nitrogen atom may form a heterocycle containing ii-5 carbon atoms in the cycle as a herbicide. Priority on the grounds: 01.O4.69 with X - triformethyl, - hydrogen, alkyl, alkenyl , alkynyl R. - alkyl, alkenyl, alkynyl or R. and R. and / or R and Rd together with the nitrogen atom can form a heterocycle containing 2-5 carbon atoms in the cycle. and R. 10 .11.69 when X is halogen, R is hydrogen; - Soo. -appRJ and R are hydrogen or C kil, and at least one of R is alkyl, and R and R together contain 3-5 carbon atoms. 10D1,69 with X - triformetil; R R is hydrogen, alkyl, alkenyl or alkynyl, and at least one of R is a hydrocarbon radical or R and R and / or R and R, together with the nitrogen atom, can form a heterocycle containing 2-5 carbon atoms in the cycle.
SU1415802A 1969-04-01 1970-03-26 Herbicide SU524493A3 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US81230769A 1969-04-01 1969-04-01
US87550769A 1969-11-10 1969-11-10
US87550869A 1969-11-10 1969-11-10

Publications (1)

Publication Number Publication Date
SU524493A3 true SU524493A3 (en) 1976-08-05

Family

ID=27420078

Family Applications (1)

Application Number Title Priority Date Filing Date
SU1415802A SU524493A3 (en) 1969-04-01 1970-03-26 Herbicide

Country Status (12)

Country Link
JP (2) JPS4843614B1 (en)
BE (1) BE748311A (en)
CH (1) CH536069A (en)
CY (1) CY719A (en)
DE (1) DE2013510C3 (en)
FR (1) FR2042189A5 (en)
GB (1) GB1268584A (en)
MY (1) MY7400054A (en)
NL (1) NL138918B (en)
OA (1) OA03243A (en)
SU (1) SU524493A3 (en)
YU (1) YU36685B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UST901009I4 (en) * 1971-06-21 1972-08-01 Defensive publication
BE787939A (en) * 1971-08-25 1973-02-26 American Cyanamid Co 2,6-DINITRANILINES HAVING HERBICIDAL PROPERTIES
JPS62238804A (en) * 1986-04-07 1987-10-19 日隈　徹 Production of freely foldable helmet and folding apparatus

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL268751A (en) * 1960-08-31
US3332769A (en) * 1963-10-07 1967-07-25 Lilly Co Eli Method of eliminating germinating and seedling weed grasses and broadleaf weeds
FR1511025A (en) * 1966-12-13 1968-01-26 Daikin Ind Ltd Process for the preparation of n, n-di (hydroxyalkyl) -2-trifluoromethyl-4,6-dinitroanilines and new products thus obtained
DE1643719A1 (en) * 1967-12-21 1971-01-28 Basf Ag Substituted dinitroanilines and herbicides containing them

Also Published As

Publication number Publication date
NL138918B (en) 1973-05-15
DE2013510B2 (en) 1978-02-02
YU36685B (en) 1984-08-31
MY7400054A (en) 1974-12-31
BE748311A (en) 1970-10-01
CH536069A (en) 1973-04-30
CY719A (en) 1974-02-05
YU85970A (en) 1982-02-25
JPS5217013B1 (en) 1977-05-12
JPS4843614B1 (en) 1973-12-19
DE2013510A1 (en) 1970-10-08
NL7004656A (en) 1970-10-05
DE2013510C3 (en) 1985-11-14
GB1268584A (en) 1972-03-29
OA03243A (en) 1970-12-15
FR2042189A5 (en) 1971-02-05

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