CS235090B2 - Herbicide or/and plant growth regulation preparation and method of its effective component production - Google Patents

Herbicide or/and plant growth regulation preparation and method of its effective component production Download PDF

Info

Publication number: CS235090B2
Authority: CS; Czechoslovakia
Prior art keywords: formula; active ingredient; composition according; compound; hydrogen
Prior art date: 1980-10-15

Application number

CS817540A

Other languages

Czech (cs)

English (en)

Inventor

Hermann Rempfler

Beat Boehner

Original Assignee

Ciba Geigy Ag

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.)

1980-10-15

Filing date

1981-10-14

Publication date

1985-04-16

1981-10-14 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1985-04-16 Publication of CS235090B2 publication Critical patent/CS235090B2/cs

Links

230000002363 herbicidal effect Effects 0.000 title claims description 18
230000008635 plant growth Effects 0.000 title claims description 11
238000000034 method Methods 0.000 title claims description 7
238000002360 preparation method Methods 0.000 title claims description 7
238000004519 manufacturing process Methods 0.000 title description 8
239000004009 herbicide Substances 0.000 title description 6
230000033228 biological regulation Effects 0.000 title 1
150000001875 compounds Chemical class 0.000 claims description 57
239000000460 chlorine Substances 0.000 claims description 27
239000000203 mixture Substances 0.000 claims description 26
239000004480 active ingredient Substances 0.000 claims description 20
-1 propionic acid acetoxime ester Chemical class 0.000 claims description 13
239000002253 acid Substances 0.000 claims description 11
229910052739 hydrogen Inorganic materials 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 10
229910052801 chlorine Inorganic materials 0.000 claims description 8
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 8
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 6
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
229910052794 bromium Chemical group 0.000 claims description 6
125000005843 halogen group Chemical group 0.000 claims description 5
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
239000000376 reactant Substances 0.000 claims description 5
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
239000011230 binding agent Substances 0.000 claims description 4
239000003795 chemical substances by application Substances 0.000 claims description 4
150000004820 halides Chemical class 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
125000001309 chloro group Chemical group Cl* 0.000 claims description 3
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210000001699 lower leg Anatomy 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
UUYSCNGPNOYZMC-UHFFFAOYSA-N methyl 2-(4-hydroxyphenoxy)propanoate Chemical compound COC(=O)C(C)OC1=CC=C(O)C=C1 UUYSCNGPNOYZMC-UHFFFAOYSA-N 0.000 description 1
JLEJCNOTNLZCHQ-UHFFFAOYSA-N methyl 2-chloropropanoate Chemical compound COC(=O)C(C)Cl JLEJCNOTNLZCHQ-UHFFFAOYSA-N 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000002808 molecular sieve Substances 0.000 description 1
LHMUZCNPQGLQPE-UHFFFAOYSA-N n-pyrrolidin-1-ylpyridin-4-amine Chemical compound C1CCCN1NC1=CC=NC=C1 LHMUZCNPQGLQPE-UHFFFAOYSA-N 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
239000006072 paste Substances 0.000 description 1
239000003415 peat Substances 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000002373 plant growth inhibitor Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
239000000047 product Substances 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
GKBJOVPKZMJZOQ-UHFFFAOYSA-N propanoic acid;propan-2-one Chemical compound CC(C)=O.CCC(O)=O GKBJOVPKZMJZOQ-UHFFFAOYSA-N 0.000 description 1
RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000005554 pyridyloxy group Chemical group 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000004576 sand Substances 0.000 description 1
230000007017 scission Effects 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
238000009331 sowing Methods 0.000 description 1
241000894007 species Species 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000003892 spreading Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
125000005207 tetraalkylammonium group Chemical group 0.000 description 1
229950011008 tetrachloroethylene Drugs 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
125000005270 trialkylamine group Chemical group 0.000 description 1
125000006387 trifluoromethyl pyridyl group Chemical group 0.000 description 1
238000009966 trimming Methods 0.000 description 1
YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
230000009105 vegetative growth Effects 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pyridine Compounds (AREA)

CS817540A 1980-10-15 1981-10-14 Herbicide or/and plant growth regulation preparation and method of its effective component production CS235090B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH769980		1980-10-15

Publications (1)

Publication Number	Publication Date
CS235090B2 true CS235090B2 (en)	1985-04-16

Family

ID=4329198

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS817540A CS235090B2 (en)	1980-10-15	1981-10-14	Herbicide or/and plant growth regulation preparation and method of its effective component production

Country Status (5)

Country	Link
JP (1)	JPS5798263A (ru)
KR (1)	KR830007558A (ru)
CS (1)	CS235090B2 (ru)
SU (1)	SU1114319A3 (ru)
ZA (1)	ZA817085B (ru)

1981
- 1981-10-14 ZA ZA817085A patent/ZA817085B/xx unknown
- 1981-10-14 SU SU813343053A patent/SU1114319A3/ru active
- 1981-10-14 CS CS817540A patent/CS235090B2/cs unknown
- 1981-10-14 KR KR1019810003882A patent/KR830007558A/ko not_active Ceased
- 1981-10-15 JP JP16491981A patent/JPS5798263A/ja active Pending

Also Published As

Publication number	Publication date
ZA817085B (en)	1982-09-29
JPS5798263A (en)	1982-06-18
KR830007558A (ko)	1983-10-21
SU1114319A3 (ru)	1984-09-15

Publication	Publication Date	Title
US4270948A (en)	1981-06-02	Herbicidal compound, herbicidal composition containing the same, and method of use thereof
CA1101867A (en)	1981-05-26	Phenoxy-alkanecarboxylic acid derivatives, their production, and their use
US4175947A (en)	1979-11-27	Phenoxy-phenoxypropionic acid esters
BG61516B2 (bg)	1997-10-31	Пропинилов естер на 2-/4-(5-хлоро-3-флуоропиридин-2-илокси) фенокси/-пропионовата киселина и приложението й
HU180704B (en)	1983-04-29	Herbicide compositions with activity for controlling groth of plants containing pyridyl-oxy-phenoxy-alkanecarboxylic acid derivatives and process for producing the active agents
WO1999045774A1 (fr)	1999-09-16	Agent regulant la croissance de vegetaux
JPH0655692B2 (ja)	1994-07-27	シクロヘキサンジオンカルボン酸誘導体、その製法及びそれを含有する組成物
US4224052A (en)	1980-09-23	Polysubstituted butanoic acids, esters and derivatives thereof utilizing the same as herbicides
KR860000321B1 (ko)	1986-04-09	퀴녹살리닐옥시 에테르의 제조방법
JPS6353176B2 (ru)	1988-10-21
EP0590045A1 (en)	1994-04-06	Substituted pyridine herbicides
DK163907B (da)	1992-04-21	Fremgangsmaade til bekaempelse af svampe og/eller bekaempelse eller regulering af plantevaekst ved hjaelp af i sidekaeden n-acylerede pyridyl-, pyrazinyl-, pyrimidinyl- eller pyridazinylderivater; i sidekaeden n-acylerede pyridyl-, pyrazinyl-, pyrimidin- og pyridazinylforbindelser til anvendelse ved fremgangsmaaden, fremgangsmaade til fremstilling af saadanne forbindelser samt fungicide og/eller plantevaekst
CN1138758C (zh)	2004-02-18	用作农药的四氢吡啶
FR2518547A1 (fr)	1983-06-24	Derives de l'acide propionique-2 phenoxy substitue et leur utilisation comme herbicides
JP2001342180A (ja)	2001-12-11	５−（１−フルオロエチル）−１−メチルピラゾール−４−カルボン酸アミド誘導体及び農園芸用の有害生物防除剤
CA1142180A (en)	1983-03-01	.alpha.-(PYRIDYL-2-OXY-PHENOXY)-PROPIONIC ACID DERIVATIVES, PROCESSES FOR PRODUCING THEM, AND THEIR USE AS HERBICIDES AND/OR AS REGULATORS OF PLANT GROWTH
JPS61229890A (ja)	1986-10-14	リン含有官能性酢酸誘導体、その製造方法およびそれらを含有する除草剤および植物生長調整剤
US4304791A (en)	1981-12-08	Benzenamines, formulations, and fungicidal method
JPH0416468B2 (ru)	1992-03-24
GB2101600A (en)	1983-01-19	2,4-Hexadienoic acid derivatives useful as weed-killers and phytogrowth regulators
CA1192555A (en)	1985-08-27	Substituted phenoxy or 2-pyridinyloxy-phenoxy- thioacetic acid derivatives
CS235090B2 (en)	1985-04-16	Herbicide or/and plant growth regulation preparation and method of its effective component production
US4280835A (en)	1981-07-28	Herbicidal N-phenyl-N-methylurea derivatives
JPH0655705B2 (ja)	1994-07-27	アシルアミノバレロニトリル誘導体、その製造法およびそれらを含有する除草剤および農園芸用殺菌剤
IL92461A (en)	1994-06-24	) S (- (1-Methoxycarbonylethyl and) S (1- Ethoxycarbonylethyl-2-chloro-5-) 2-chloro-4-trifluoromethylphenoxy (benzoates, their preparation and use as herbicides