CH563120A5 - Benztriazinonylmethyl organophosphorus esters - insecticides acaricides, fungicides, bactericides and nematocides - Google Patents

Benztriazinonylmethyl organophosphorus esters - insecticides acaricides, fungicides, bactericides and nematocides

Info

Publication number: CH563120A5
Authority: CH; Switzerland
Prior art keywords: parts; formula; compounds; active ingredient; sep
Prior art date: 1971-12-23

Application number

CH1882771A

Other languages

German (de)

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.)

1971-12-23

Filing date

1971-12-23

Publication date

1975-06-30

Priority to BE793208D priority Critical patent/BE793208A/xx

1971-12-23 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1971-12-23 Priority to CH1882771A priority patent/CH563120A5/de

1972-11-21 Priority to TR1711072A priority patent/TR17110A/tr

1972-12-12 Priority to IL41066A priority patent/IL41066A/en

1972-12-14 Priority to NL7217028A priority patent/NL7217028A/xx

1972-12-14 Priority to AU50097/72A priority patent/AU5009772A/en

1972-12-20 Priority to DE2262517A priority patent/DE2262517A1/de

1972-12-20 Priority to EG526/72A priority patent/EG10794A/xx

1972-12-21 Priority to BG022186A priority patent/BG20529A3/xx

1972-12-22 Priority to FR7245940A priority patent/FR2164884B1/fr

1972-12-22 Priority to ES409945A priority patent/ES409945A1/es

1972-12-22 Priority to GB5951272A priority patent/GB1394890A/en

1972-12-22 Priority to OA54789A priority patent/OA04300A/xx

1972-12-22 Priority to IT33545/72A priority patent/IT988579B/it

1972-12-22 Priority to CA159,827A priority patent/CA997348A/en

1972-12-22 Priority to AT1097672A priority patent/AT316927B/de

1972-12-22 Priority to HUCI001324 priority patent/HU166051B/hu

1972-12-22 Priority to DD167833A priority patent/DD103797A5/xx

1972-12-23 Priority to JP48004210A priority patent/JPS4868746A/ja

1975-01-29 Priority to US05/544,982 priority patent/US3969517A/en

1975-06-30 Publication of CH563120A5 publication Critical patent/CH563120A5/de

Links

-1 Benztriazinonylmethyl Chemical group 0.000 title abstract description 13
230000000895 acaricidal effect Effects 0.000 title description 6
239000000642 acaricide Substances 0.000 title description 3
150000002148 esters Chemical class 0.000 title description 3
239000002917 insecticide Substances 0.000 title description 3
230000000844 anti-bacterial effect Effects 0.000 title description 2
239000000417 fungicide Substances 0.000 title description 2
230000001069 nematicidal effect Effects 0.000 title description 2
239000003899 bactericide agent Substances 0.000 title 1
239000005645 nematicide Substances 0.000 title 1
150000001875 compounds Chemical group 0.000 claims description 27
239000003795 chemical substances by application Substances 0.000 claims description 9
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
241000238631 Hexapoda Species 0.000 claims description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
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230000001419 dependent effect Effects 0.000 claims 3
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150000003839 salts Chemical class 0.000 abstract description 6
125000000217 alkyl group Chemical group 0.000 abstract description 2
XZRYWLBAUQTTMJ-UHFFFAOYSA-N 5-(chloromethyl)-3H-1,2,3-benzotriazin-4-one Chemical compound ClCC1=CC=CC2=C1C(NN=N2)=O XZRYWLBAUQTTMJ-UHFFFAOYSA-N 0.000 abstract 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 1
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OWQPOVKKUWUEKE-UHFFFAOYSA-N 1,2,3-benzotriazine Chemical compound N1=NN=CC2=CC=CC=C21 OWQPOVKKUWUEKE-UHFFFAOYSA-N 0.000 description 1
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IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
230000002464 fungitoxic effect Effects 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000005469 granulation Methods 0.000 description 1
230000003179 granulation Effects 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N heptadecan-1-ol Chemical class CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical class CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
150000004678 hydrides Chemical class 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
239000005457 ice water Substances 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
230000001418 larval effect Effects 0.000 description 1
230000002045 lasting effect Effects 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000004571 lime Substances 0.000 description 1
239000006028 limestone Substances 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
235000012245 magnesium oxide Nutrition 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
231100001184 nonphytotoxic Toxicity 0.000 description 1
230000009965 odorless effect Effects 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
239000003791 organic solvent mixture Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
230000003071 parasitic effect Effects 0.000 description 1
239000002245 particle Substances 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
235000019422 polyvinyl alcohol Nutrition 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
229940072033 potash Drugs 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
235000015320 potassium carbonate Nutrition 0.000 description 1
238000012545 processing Methods 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
239000002002 slurry Substances 0.000 description 1
235000017550 sodium carbonate Nutrition 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
SRAWNDFHGTVUNZ-UHFFFAOYSA-M sodium;3,6-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(CCCC)=CC2=CC(CCCC)=CC=C21 SRAWNDFHGTVUNZ-UHFFFAOYSA-M 0.000 description 1
238000002336 sorption--desorption measurement Methods 0.000 description 1
241000894007 species Species 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
229910052682 stishovite Inorganic materials 0.000 description 1
239000000725 suspension Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
125000005270 trialkylamine group Chemical group 0.000 description 1
229910052905 tridymite Inorganic materials 0.000 description 1
PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
239000002023 wood Substances 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having three nitrogen atoms as the only ring hetero atoms
- C07F9/6521—Six-membered rings
- C07F9/65218—Six-membered rings condensed with carbocyclic rings or carbocyclic ring systems

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

CH1882771A 1971-12-23 1971-12-23 Benztriazinonylmethyl organophosphorus esters - insecticides acaricides, fungicides, bactericides and nematocides CH563120A5 (en)

Priority Applications (20)

Application Number	Priority Date	Filing Date	Title
BE793208D BE793208A (fr)	1971-12-23		Esters d'acides thiophosphoriques et produits pesticides qui encontiennent
CH1882771A CH563120A5 (en)	1971-12-23	1971-12-23	Benztriazinonylmethyl organophosphorus esters - insecticides acaricides, fungicides, bactericides and nematocides
TR1711072A TR17110A (tr)	1971-12-23	1972-11-21	Yeni esterler
IL41066A IL41066A (en)	1971-12-23	1972-12-12	Benzotriazinonylmethyl dithiophosphoric esters their manufacture and their use as pesticides
NL7217028A NL7217028A (tr)	1971-12-23	1972-12-14
AU50097/72A AU5009772A (en)	1971-12-23	1972-12-14	Benztriazinonylmethyl-organophosphoric esters
DE2262517A DE2262517A1 (de)	1971-12-23	1972-12-20	Neue ester
EG526/72A EG10794A (en)	1971-12-23	1972-12-20	Benztriazinonylmethyl organophosphoric esters,their use as insecticides
BG022186A BG20529A3 (bg)	1971-12-23	1972-12-21	Инсектицидно и акарицидно средство
FR7245940A FR2164884B1 (tr)	1971-12-23	1972-12-22
ES409945A ES409945A1 (es)	1971-12-23	1972-12-22	Procedimiento para la preparacion de esteres de benzotira- cinonil-metil-organofosforo.
GB5951272A GB1394890A (en)	1971-12-23	1972-12-22	Pesticidal dithiophosphoric acid esters
OA54789A OA04300A (fr)	1971-12-23	1972-12-22	Esters d'acides thiophosphoriques et produits pesticides qui en contiennent.
IT33545/72A IT988579B (it)	1971-12-23	1972-12-22	Esteri benzotriarononil metil organo fosforici ad azione insetticida
CA159,827A CA997348A (en)	1971-12-23	1972-12-22	Benzotriazonylmethyl-organophosphoric esters
AT1097672A AT316927B (de)	1971-12-23	1972-12-22	Insektizide und akarizide Mittel
HUCI001324 HU166051B (tr)	1971-12-23	1972-12-22
DD167833A DD103797A5 (tr)	1971-12-23	1972-12-22
JP48004210A JPS4868746A (tr)	1971-12-23	1972-12-23
US05/544,982 US3969517A (en)	1971-12-23	1975-01-29	Asymmetric O,S-dialkyl dithiophosphoric acid esters of 1,2,3-benzotriazin-4-ones

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1882771A CH563120A5 (en)	1971-12-23	1971-12-23	Benztriazinonylmethyl organophosphorus esters - insecticides acaricides, fungicides, bactericides and nematocides

Publications (1)

Publication Number	Publication Date
CH563120A5 true CH563120A5 (en)	1975-06-30

Family

ID=4435502

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1882771A CH563120A5 (en)	1971-12-23	1971-12-23	Benztriazinonylmethyl organophosphorus esters - insecticides acaricides, fungicides, bactericides and nematocides

Country Status (4)

Country	Link
AU (1)	AU5009772A (tr)
CH (1)	CH563120A5 (tr)
HU (1)	HU166051B (tr)
TR (1)	TR17110A (tr)

1971
- 1971-12-23 CH CH1882771A patent/CH563120A5/de not_active IP Right Cessation
1972
- 1972-11-21 TR TR1711072A patent/TR17110A/tr unknown
- 1972-12-14 AU AU50097/72A patent/AU5009772A/en not_active Expired
- 1972-12-22 HU HUCI001324 patent/HU166051B/hu unknown

Also Published As

Publication number	Publication date
TR17110A (tr)	1974-04-25
HU166051B (tr)	1974-12-28
AU5009772A (en)	1974-06-20

Legal Events

Date	Code	Title	Description
1981-08-31	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DE2259960C2 (de)	1983-03-03	1.2.4-Triazolyl-(thiono)-phosphor(phosphon)-säureester, Verfahren zu ihrer Herstellung und diese enthaltende Schädlingsbekämpfungsmittel
CH574214A5 (tr)	1976-04-15
DE2330089C2 (de)	1983-03-24	1.2.4-Triazolyl-(thiono)-phosphor(phosphon)-säurederivate, Verfahren zu ihrer Herstellung sowie diese enthaltende Schädlingsbekämpfungsmittel
DE2422324C2 (de)	1984-05-03	Diphenyläther-phosphorverbindungen, Verfahren zu ihrer Herstellung und diese enthaltende Schädlingsbekämpfungsmittel
CH580910A5 (tr)	1976-10-29
CH604522A5 (en)	1978-09-15	(4,5)-Benzospiro-(2,4)-heptane-(1)-carboxylate esters
CH643563A5 (en)	1984-06-15	1,3-Diaza-2-phosphacyclohexane derivatives
CH576226A5 (en)	1976-06-15	Aralkyl phenyl ethers and thioethers - with acaricidal and insecticidal activity
CH569415A5 (en)	1975-11-28	Thiophosphate esters - insecticides,acaricides,fungistats and bacteriostats
CH563119A5 (en)	1975-06-30	S-benzyl dithiophosphoric esters - insecticides and acaricides
CH570112A5 (en)	1975-12-15	Organophosphorus pesticides - contg. O-(2-phenoxy-phenyl) dithiophosphates
CH590612A5 (en)	1977-08-15	Pesticidal compsns. contg. organophosphorus amidines - useful for control of insect and acarid parasites on plants and animals
CH576232A5 (en)	1976-06-15	Thiophosphate esters - insecticides,acaricides,fungistats and bacteriostats
CH581434A5 (en)	1976-11-15	Cyanophenyl-thiolphosphates - insecticides and acaricides
CH582993A5 (en)	1976-12-31	S'-(midomethylene)s-alkyl s-alkyldithiophosphoric esters - - insecticides, acaricides, nematocides and fungicides
CH564307A5 (en)	1975-07-31	Subst phenyl (di) thiophosphates - wi h pesticidal activity
CH571304A5 (en)	1976-01-15	Subst. formamidine derivs prepn - with biocidal activity
CH573206A5 (en)	1976-03-15	Pesticidal 5-halo-1,2,4-triazol-3-yl carbamates - e.g. 1-isopropyl-5-chloro-1,2,4-triazol-3-yl dimethylcarbamate
CH575717A5 (en)	1976-05-31	S-Arylthioalkyl-O,S-dialkyl dithiophosphates - with insecticidal, acaricidal, fungicidal, nematocidal activity, etc.
CH570763A5 (en)	1975-12-31	Azobenzene organophosphorus esters - useful as insecticides and acaricides
CH574713A5 (en)	1976-04-30	s-Picolyl phosphoridithioates - useful as insecticides, acaricides and plant-growth regulators
CH561018A5 (en)	1975-04-30	S-carbamoylalkyl o-ethyl s-n-propyldithio-phosphoric acid - esters - in insecticides, acaricides, fungicides, bactericides plant
CH571809A5 (en)	1976-01-30	Subst. formamidine derivs prepn - with biocidal activity
DE2418270A1 (de)	1974-10-24	Thiolphosphorsaeureester, verfahren zu ihrer herstellung und ihre verwendung
CH581429A5 (en)	1976-11-15	Pesticidal subst. benzyl (thio)ethers - prepd. by reacting subst. benzyl halides or sulphonates with (thio)phenols