DD233065A5 - Fungizide mittel und verfahren zur bekaempfung von phytotoxischen pilzen - Google Patents

Fungizide mittel und verfahren zur bekaempfung von phytotoxischen pilzen Download PDF

Info

Publication number: DD233065A5
Authority: DD; German Democratic Republic
Prior art keywords: trifluoromethyl; nitro; weight; phenoxy; benzaldehyde
Prior art date: 1984-01-17

Application number

DD23306585A

Other languages

German (de)

English (en)

Inventor

Jozsef Bakos

Balint Heil

Laszlo Kollar

Szilard Toeroes

Gyula Eifert

Ferenc Bihari

Janos Sulagyi

Anna Durko

Istvan Kueronya

Istvan Magyari

Katalin Tromfos

Peter Bohus

Laszlo Wohl

Original Assignee

Budapesti Vegyimuevek

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.)

1984-01-17

Filing date

1985-01-17

Publication date

1986-02-19

1985-01-17 Application filed by Budapesti Vegyimuevek filed Critical Budapesti Vegyimuevek

1986-02-19 Publication of DD233065A5 publication Critical patent/DD233065A5/de

Links

239000000417 fungicide Substances 0.000 title claims abstract description 6
238000000034 method Methods 0.000 title claims description 5
231100000208 phytotoxic Toxicity 0.000 title claims description 4
230000000885 phytotoxic effect Effects 0.000 title claims description 4
239000004480 active ingredient Substances 0.000 claims abstract description 14
239000001257 hydrogen Substances 0.000 claims abstract description 9
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 9
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 8
IMPIIVKYTNMBCD-UHFFFAOYSA-N 2-phenoxybenzaldehyde Chemical class O=CC1=CC=CC=C1OC1=CC=CC=C1 IMPIIVKYTNMBCD-UHFFFAOYSA-N 0.000 claims abstract description 5
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 3
239000000460 chlorine Chemical group 0.000 claims abstract description 3
229910052801 chlorine Chemical group 0.000 claims abstract description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 4
-1 5-chloro-4-trifluoromethyl-2-nitro-phenoxy Chemical group 0.000 claims description 20
241000233866 Fungi Species 0.000 claims description 9
239000003795 chemical substances by application Substances 0.000 claims description 7
239000000546 pharmaceutical excipient Substances 0.000 claims description 4
NXAJMYURNVZHLB-UHFFFAOYSA-N 3-[2,6-dinitro-4-(trifluoromethyl)phenoxy]benzaldehyde Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=CC([N+]([O-])=O)=C1OC1=CC=CC(C=O)=C1 NXAJMYURNVZHLB-UHFFFAOYSA-N 0.000 claims description 3
UCDTUCPKRHTAAQ-UHFFFAOYSA-N 3-[3-(3-formylphenoxy)-2,4-dinitro-6-(trifluoromethyl)phenoxy]benzaldehyde Chemical compound C(=O)C=1C=C(OC2=C(C=C(C(=C2[N+](=O)[O-])OC2=CC(=CC=C2)C=O)[N+](=O)[O-])C(F)(F)F)C=CC=1 UCDTUCPKRHTAAQ-UHFFFAOYSA-N 0.000 claims 1
NXGAWPRHTYNHPD-UHFFFAOYSA-N 5-[2,6-dinitro-4-(trifluoromethyl)phenoxy]-2-nitrobenzaldehyde Chemical compound C1=C(C=O)C([N+](=O)[O-])=CC=C1OC1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O NXGAWPRHTYNHPD-UHFFFAOYSA-N 0.000 claims 1
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239000010440 gypsum Substances 0.000 description 1
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238000010438 heat treatment Methods 0.000 description 1
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239000004009 herbicide Substances 0.000 description 1
239000012456 homogeneous solution Substances 0.000 description 1
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150000002576 ketones Chemical class 0.000 description 1
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YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
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125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
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ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
150000002889 oleic acids Chemical class 0.000 description 1
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239000011368 organic material Substances 0.000 description 1
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230000000361 pesticidal effect Effects 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
150000008094 phenoxybenzenes Chemical class 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
239000000049 pigment Substances 0.000 description 1
230000010152 pollination Effects 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000010802 sludge Substances 0.000 description 1
229920005552 sodium lignosulfonate Polymers 0.000 description 1
229940048842 sodium xylenesulfonate Drugs 0.000 description 1
DGSDBJMBHCQYGN-UHFFFAOYSA-M sodium;2-ethylhexyl sulfate Chemical compound [Na+].CCCCC(CC)COS([O-])(=O)=O DGSDBJMBHCQYGN-UHFFFAOYSA-M 0.000 description 1
QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 1
RVULBHWZFCBODE-UHFFFAOYSA-M sodium;5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate Chemical compound [Na+].C1=C([N+]([O-])=O)C(C(=O)[O-])=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 RVULBHWZFCBODE-UHFFFAOYSA-M 0.000 description 1
HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
238000010186 staining Methods 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008107 starch Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
239000002600 sunflower oil Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
229950011008 tetrachloroethylene Drugs 0.000 description 1
230000008719 thickening Effects 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
229940078499 tricalcium phosphate Drugs 0.000 description 1
229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
235000019731 tricalcium phosphate Nutrition 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical group OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
NQPDZGIKBAWPEJ-UHFFFAOYSA-M valerate Chemical compound CCCCC([O-])=O NQPDZGIKBAWPEJ-UHFFFAOYSA-M 0.000 description 1
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/27—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
- C07C205/35—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C205/36—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system
- C07C205/38—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system the oxygen atom of at least one of the etherified hydroxy groups being further bound to a carbon atom of a six-membered aromatic ring, e.g. nitrodiphenyl ethers
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing aliphatically bound aldehyde or keto groups, or thio analogues thereof; Derivatives thereof, e.g. acetals
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/44—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by —CHO groups

Landscapes

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

DD23306585A 1984-01-17 1985-01-17 Fungizide mittel und verfahren zur bekaempfung von phytotoxischen pilzen DD233065A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
HU15884A HU193194B (en)	1984-01-17	1984-01-17	Fungicide compositions containing phenoxy-benzaldehyde derivatives as active substances and process for preparing the active substances

Publications (1)

Publication Number	Publication Date
DD233065A5 true DD233065A5 (de)	1986-02-19

Family

ID=10948239

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
DD23306585A DD233065A5 (de)	1984-01-17	1985-01-17	Fungizide mittel und verfahren zur bekaempfung von phytotoxischen pilzen
DD27262485A DD231345A5 (de)	1984-01-17	1985-01-17	Phenoxybenzaldehid-derivate

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
DD27262485A DD231345A5 (de)	1984-01-17	1985-01-17	Phenoxybenzaldehid-derivate

Country Status (9)

Country	Link
JP (1)	JPS60237038A (cs)
CH (1)	CH663409A5 (cs)
CS (1)	CS249535B2 (cs)
DD (2)	DD233065A5 (cs)
DE (1)	DE3501428A1 (cs)
FR (1)	FR2558155B1 (cs)
GB (1)	GB2154235B (cs)
HU (1)	HU193194B (cs)
YU (1)	YU6185A (cs)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
HU193467B (en) *	1984-11-12	1987-10-28	Budapesti Vegyimuevek	Fungicidal composition comprising substituted benzoic acid derivative as active substance and process for preparing the active substance
US6028219A (en) *	1995-09-13	2000-02-22	Zeneca Limited	Process for the nitration of diphenylethers
MX2007004400A (es) *	2004-10-13	2007-06-19	Glenmark Pharmaceuticals Sa	Procedimiento para la preparacion de n-(3,5-dicloropirid-a-il)-4- ifluorometoxi-8-metanosulfonamido-dibenzo [b,d] difuran-1-carboxamida.

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB2050168B (en) *	1979-04-04	1982-11-10	Shell Int Research	Ethynyl compounds as herbicides

1984
- 1984-01-17 HU HU15884A patent/HU193194B/hu unknown
1985
- 1985-01-15 CH CH17985A patent/CH663409A5/de not_active IP Right Cessation
- 1985-01-16 GB GB08501038A patent/GB2154235B/en not_active Expired
- 1985-01-17 DD DD23306585A patent/DD233065A5/de not_active IP Right Cessation
- 1985-01-17 FR FR8500641A patent/FR2558155B1/fr not_active Expired
- 1985-01-17 CS CS33785A patent/CS249535B2/cs unknown
- 1985-01-17 DD DD27262485A patent/DD231345A5/de not_active IP Right Cessation
- 1985-01-17 DE DE19853501428 patent/DE3501428A1/de not_active Withdrawn
- 1985-01-17 JP JP513185A patent/JPS60237038A/ja active Pending
- 1985-01-17 YU YU6185A patent/YU6185A/xx unknown

Also Published As

Publication number	Publication date
DE3501428A1 (de)	1985-07-18
FR2558155B1 (fr)	1987-04-24
CH663409A5 (de)	1987-12-15
HUT37907A (en)	1986-03-28
FR2558155A1 (fr)	1985-07-19
YU6185A (en)	1988-02-29
GB2154235B (en)	1987-07-08
HU193194B (en)	1987-08-28
GB8501038D0 (en)	1985-02-20
CS249535B2 (en)	1987-03-12
JPS60237038A (ja)	1985-11-25
DD231345A5 (de)	1985-12-24
GB2154235A (en)	1985-09-04

Legal Events

Date	Code	Title	Description
1994-01-27	PJ	Ceased due to non-payment of renewal fee (addendum to changes before extension act)

Publication	Publication Date	Title
DD232184A5 (de)	1986-01-22	Pestizide zusammensetzung
DE2509416A1 (de)	1975-09-25	Dinitrobenzotrifluoride
DE2130030A1 (de)	1972-12-21	Fungizide und bakterizide Mittel
DE1955750A1 (de)	1971-05-13	Ureidophenylguanidine,Verfahren zu ihrer Herstellung und ihre fungizide Verwendung
EP0110829B1 (de)	1990-12-27	Schädlingsbekämpfungsmittel
DE2213081A1 (de)	1972-09-28	Diphenylamine, deren Herstellung und deren Verwendung als Pesticide
DE2136923A1 (de)	1973-02-01	Substituierte benzthiazole, verfahren zu ihrer herstellung und ihre verwendung als fungizide und bakterizide
DE2243626A1 (de)	1974-03-14	N-sulfenylierte carbamidoxime, verfahren zu ihrer herstellung und ihre fungizide und bakterizide verwendung
DD233065A5 (de)	1986-02-19	Fungizide mittel und verfahren zur bekaempfung von phytotoxischen pilzen
DD229013A5 (de)	1985-10-30	Fungizide mittel
EP0001623B1 (de)	1980-09-03	Aryl-thiocarbonsäure-thiocyanmethylester, ihre Herstellung und ihre Verwendung als Pestizide, sowie sie enthaltende Mittel
DE2609704A1 (de)	1976-09-23	Thioamidverbindungen, verfahren zu ihrer herstellung und ihre verwendung zur schaedlingsbekaempfung
EP0077300B1 (de)	1985-02-13	Triorganozinnhydantoin-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung
DE2331183A1 (de)	1975-01-16	1-alkoxycarbonyl-2-(n-alkoxycarbonyln-acyl-amino)-benzimidazole, verfahren zu ihrer herstellung, sowie ihre verwendung als fungizide
DD259125A5 (de)	1988-08-17	Pestizide mittel
DE2242785A1 (de)	1974-03-14	1-alkylsulfonyl-2-trifluormethylbenzimidazole, verfahren zu ihrer herstellung sowie ihre verwendung als ektoparasitenmittel
DD239711A5 (de)	1986-10-08	Fungizide zusammensetzung
EP0053096A1 (de)	1982-06-02	Unsymmetrische Bis-Carbamate, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung
AT324045B (de)	1975-08-11	Insektizide und akarizide zusammensetzungen
AT275966B (de)	1969-11-10	Fungitoxisches Mittel für den Pflanzenschutz
EP0056217A1 (de)	1982-07-21	2-Methyl-4-N,N-dimethylcarbamoyloxy-6-amino-pyrimidine und deren Salze, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung
DE2548450A1 (de)	1976-05-13	Schaedlingsbekaempfungsmittel
EP0041920A2 (de)	1981-12-16	Neue Organophosphate
EP0080435A2 (de)	1983-06-01	4-N,N-Dimethylcarbamoyloxy-6-aminopyrimidine und ihre Salze, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung
EP0164308A1 (de)	1985-12-11	N-Formyl-dithiophosphonsäureamide