IL29306A - Substituted diphenyl ethers and pesticidal preparations containing them - Google Patents

Substituted diphenyl ethers and pesticidal preparations containing them

Info

Publication number: IL29306A
Authority: IL; Israel
Prior art keywords: parts; active substance; active; preparations containing; diphenyl ethers
Prior art date: 1967-01-20

Application number

IL29306A

Other languages

English (en)

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.)

1967-01-20

Filing date

1968-01-12

Publication date

1971-12-29

1968-01-12 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1971-12-29 Publication of IL29306A publication Critical patent/IL29306A/en

Links

238000002360 preparation method Methods 0.000 title claims description 10
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 title 1
230000000361 pesticidal effect Effects 0.000 title 1
150000001875 compounds Chemical class 0.000 claims description 6
241000607479 Yersinia pestis Species 0.000 claims description 3
239000013543 active substance Substances 0.000 description 27
239000000203 mixture Substances 0.000 description 10
230000001069 nematicidal effect Effects 0.000 description 9
239000000126 substance Substances 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
239000000839 emulsion Substances 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
239000007787 solid Substances 0.000 description 4
239000000243 solution Substances 0.000 description 4
241000244206 Nematoda Species 0.000 description 3
238000005266 casting Methods 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000000047 product Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000000725 suspension Substances 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
239000011575 calcium Substances 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
238000010410 dusting Methods 0.000 description 2
HTAATVDZOHXHBE-UHFFFAOYSA-N methyl 10-formyl-3,9-dihydroxy-1,4,7-trimethyl-6-oxobenzo[b][1,4]benzodioxepine-2-carboxylate Chemical compound O1C2=C(C=O)C(O)=CC(C)=C2C(=O)OC2=C1C(C)=C(C(=O)OC)C(O)=C2C HTAATVDZOHXHBE-UHFFFAOYSA-N 0.000 description 2
239000004576 sand Substances 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
239000002689 soil Substances 0.000 description 2
UAZUEJTXWAXSMA-UHFFFAOYSA-N 1,1-dichlorobut-1-ene Chemical compound CCC=C(Cl)Cl UAZUEJTXWAXSMA-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
239000004254 Ammonium phosphate Substances 0.000 description 1
KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
241000195493 Cryptophyta Species 0.000 description 1
241000399934 Ditylenchus Species 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
241000233866 Fungi Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
239000005864 Sulphur Substances 0.000 description 1
BREXUOXCEDKPCA-UHFFFAOYSA-N [Ca].OB(O)O Chemical compound [Ca].OB(O)O BREXUOXCEDKPCA-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
ZRIUUUJAJJNDSS-UHFFFAOYSA-N ammonium phosphates Chemical class [NH4+].[NH4+].[NH4+].[O-]P([O-])([O-])=O ZRIUUUJAJJNDSS-UHFFFAOYSA-N 0.000 description 1
235000019289 ammonium phosphates Nutrition 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
235000011010 calcium phosphates Nutrition 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
235000011009 potassium phosphates Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical class [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
239000002699 waste material Substances 0.000 description 1
235000020681 well water Nutrition 0.000 description 1
239000002349 well water Substances 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/54—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and etherified hydroxy groups bound to the carbon skeleton

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

IL29306A 1967-01-20 1968-01-12 Substituted diphenyl ethers and pesticidal preparations containing them IL29306A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH88667A CH481571A (de)	1967-01-20	1967-01-20	Schädlingsbekämpfungsmittel

Publications (1)

Publication Number	Publication Date
IL29306A true IL29306A (en)	1971-12-29

Family

ID=4197461

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL29306A IL29306A (en)	1967-01-20	1968-01-12	Substituted diphenyl ethers and pesticidal preparations containing them

Country Status (7)

Country	Link
US (1)	US3766238A (de)
CH (1)	CH481571A (de)
DE (1)	DE1693192A1 (de)
FR (1)	FR1573898A (de)
GB (1)	GB1189594A (de)
IL (1)	IL29306A (de)
NL (1)	NL6800885A (de)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3966453A (en) *	1972-01-27	1976-06-29	Ishihara Sangyo Kaisha Ltd.	Herbicidal 2-halo-4-trifluoromethyl-4'-cyanophenyl-ethers
US4046798A (en) *	1973-02-12	1977-09-06	Rohm And Haas Company	Herbicidal 4-trifluoromethyl-4'nitrodiphenyl ethers
US4091109A (en) *	1976-06-18	1978-05-23	Nippon Kayaku Kabushiki Kaisha	Diphenylether derivatives and use thereof as an acaricide
US4350522A (en) *	1977-06-20	1982-09-21	Rohm And Haas Company	Herbicidal 4-trifluoromethyl-4'-nitrodiphenyl ethers
US4332820A (en) *	1980-01-25	1982-06-01	The Dow Chemical Company	Substituted benzonitriles having antiviral activity
US4254144A (en) *	1980-01-25	1981-03-03	The Dow Chemical Company	Substituted benzonitriles having antiviral activity
US4505929A (en) *	1980-06-12	1985-03-19	The Dow Chemical Company	Sulfur-substituted diphenyl ethers having antiviral activity
US4349568A (en) *	1980-06-12	1982-09-14	The Dow Chemical Company	Sulfur-substituted diphenyl ethers having antiviral activity
JPS6341451A (ja) *	1986-08-06	1988-02-22	Nippon Kayaku Co Ltd	エ−テル誘導体およびそれを有効成分とする殺ダニ、殺虫組成物

1967
- 1967-01-20 CH CH88667A patent/CH481571A/de not_active IP Right Cessation
1968
- 1968-01-11 DE DE19681693192 patent/DE1693192A1/de active Pending
- 1968-01-12 IL IL29306A patent/IL29306A/en unknown
- 1968-01-16 FR FR1573898D patent/FR1573898A/fr not_active Expired
- 1968-01-19 NL NL6800885A patent/NL6800885A/xx unknown
- 1968-01-22 GB GB3193/68A patent/GB1189594A/en not_active Expired
1970
- 1970-11-19 US US00091172A patent/US3766238A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
FR1573898A (de)	1969-07-11
DE1693192A1 (de)	1971-06-03
CH481571A (de)	1969-11-30
NL6800885A (de)	1968-07-22
US3766238A (en)	1973-10-16
GB1189594A (en)	1970-04-29

Publication	Publication Date	Title
JPS6045508A (ja)	1985-03-12	菌類病害に対するブドウ保護用殺菌剤組成物
DE1048737B (de)	1959-01-15
US3189428A (en)	1965-06-15	Method for inhibiting plant growth
US3766238A (en)	1973-10-16	3-nitro-4-phenoxy benzonitriles
IL29305A (en)	1971-07-28	Pesticidal preparations containing diaralkyl amines
DE1147796B (de)	1963-04-25	Mittel zur Bekaempfung von pflanzenparasitaeren Nematoden
US3642989A (en)	1972-02-15	Nematocidal preparations containing phosphonium compounds as the ingredient
US2954318A (en)	1960-09-27	Miticide composition
US3008869A (en)	1961-11-14	Nematocide compositions
US2934420A (en)	1960-04-26	Pesticidal and herbicidal compositions of matter
CS241143B2 (en)	1986-03-13	Fungicide
DE1445824B1 (de)	1969-11-13	1,3,4-Thiadiazolderivate und ihre Verwendung als nematozide Mittel
US2745729A (en)	1956-05-15	Herbicidal composition
US2940896A (en)	1960-06-14	Quaternary ammonium and phosphoramide ester attractants and insect control therewith
US5073647A (en)	1991-12-17	Reduction and inhibition of etu content in alkylenebisdithiocarbamates
DE1301819B (de)	1969-08-28	Substituierte 2, 4-Diamino-6-chlor-s-triazine
DE2141227A1 (de)	1972-02-24	Carbamoyloximverbindungen sowie deren Verwendung
US3700778A (en)	1972-10-24	Insecticidal composition containing trifluoromethyl substituted benzanilides and method of using the same
DE2425237A1 (de)	1974-12-12	Organophosphorverbindungen
SU537611A3 (ru)	1976-11-30	Гербицидный состав
DE944404C (de)	1956-08-16	Insektenbekaempfungsmittel
DE1445824C (de)
US3129136A (en)	1964-04-14	Controlling nematodes with 2-chloro-3-hydroxy-4-nitro-benzaldehyde
US3810982A (en)	1974-05-14	Insecticidal phosphonyl cyanodithioimido carbonates
SU628818A3 (ru)	1978-10-15	Инсектицидное средство