CH572308A5 - Pesticidal phosphorothiolates and-thiolothionates - O-(m)ethyl-5-propyl or butyl-O-substd phenyl-phosphorothiolates and-thiolothionates are insecticides, acaracides and fungicides - Google Patents

Pesticidal phosphorothiolates and-thiolothionates - O-(m)ethyl-5-propyl or butyl-O-substd phenyl-phosphorothiolates and-thiolothionates are insecticides, acaracides and fungicides

Info

Publication number: CH572308A5
Authority: CH; Switzerland
Prior art keywords: sep; alkyl; larvae; formula; test
Prior art date: 1972-11-03

Application number

CH1604372A

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.)

1972-11-03

Filing date

1972-11-03

Publication date

1976-02-13

1972-11-03 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1972-11-03 Priority to CH1604372A priority Critical patent/CH572308A5/de

1973-10-16 Priority to CA183,449A priority patent/CA1058192A/fr

1973-10-22 Priority to IL43458A priority patent/IL43458A/en

1973-10-23 Priority to AU61705/73A priority patent/AU480851B2/en

1973-10-23 Priority to NL7314564A priority patent/NL7314564A/xx

1973-10-23 Priority to US408874A priority patent/US3898305A/en

1973-10-30 Priority to OA55050A priority patent/OA04500A/fr

1973-10-31 Priority to BE137301A priority patent/BE806794A/fr

1973-10-31 Priority to FR7338840A priority patent/FR2205526B1/fr

1973-10-31 Priority to DE19732354653 priority patent/DE2354653A1/de

1973-11-01 Priority to EG414/73A priority patent/EG11386A/xx

1973-11-01 Priority to TR17851A priority patent/TR17851A/xx

1973-11-02 Priority to GB5107073A priority patent/GB1441639A/en

1973-11-02 Priority to JP48123910A priority patent/JPS4975732A/ja

1973-11-02 Priority to AT924773A priority patent/AT324772B/de

1973-11-02 Priority to ZA738449A priority patent/ZA738449B/xx

1974-12-20 Priority to US05/534,594 priority patent/US3943202A/en

1974-12-20 Priority to US05/534,933 priority patent/US3935233A/en

1974-12-20 Priority to US05/534,591 priority patent/US3991141A/en

1975-05-19 Priority to US05/578,960 priority patent/US4017612A/en

1976-02-13 Publication of CH572308A5 publication Critical patent/CH572308A5/de

1976-12-17 Priority to US05/751,918 priority patent/US4262012A/en

Links

239000002917 insecticide Substances 0.000 title description 2
239000000417 fungicide Substances 0.000 title 1
230000000361 pesticidal effect Effects 0.000 title 1
125000000217 alkyl group Chemical group 0.000 claims abstract description 7
229910052801 chlorine Inorganic materials 0.000 claims abstract description 7
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 7
229910052760 oxygen Inorganic materials 0.000 claims abstract description 6
229910052794 bromium Inorganic materials 0.000 claims abstract description 5
229910052717 sulfur Inorganic materials 0.000 claims abstract description 4
150000001875 compounds Chemical class 0.000 claims description 28
238000012360 testing method Methods 0.000 claims description 23
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 19
230000000694 effects Effects 0.000 claims description 16
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 14
239000000460 chlorine Substances 0.000 claims description 12
239000004480 active ingredient Substances 0.000 claims description 10
241000238876 Acari Species 0.000 claims description 8
241000426497 Chilo suppressalis Species 0.000 claims description 6
235000013601 eggs Nutrition 0.000 claims description 6
239000000839 emulsion Substances 0.000 claims description 6
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
150000002431 hydrogen Chemical class 0.000 claims description 6
230000000749 insecticidal effect Effects 0.000 claims description 6
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 6
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
239000003795 chemical substances by application Substances 0.000 claims description 5
239000008187 granular material Substances 0.000 claims description 5
239000000203 mixture Substances 0.000 claims description 5
239000001301 oxygen Substances 0.000 claims description 5
239000007921 spray Substances 0.000 claims description 5
241001425390 Aphis fabae Species 0.000 claims description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
241000196324 Embryophyta Species 0.000 claims description 4
244000046052 Phaseolus vulgaris Species 0.000 claims description 4
241000949016 Rhipicephalus bursa Species 0.000 claims description 4
241000238680 Rhipicephalus microplus Species 0.000 claims description 4
241001454295 Tetranychidae Species 0.000 claims description 4
241001454293 Tetranychus urticae Species 0.000 claims description 4
240000006677 Vicia faba Species 0.000 claims description 4
235000010749 Vicia faba Nutrition 0.000 claims description 4
230000000895 acaricidal effect Effects 0.000 claims description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
238000010790 dilution Methods 0.000 claims description 4
239000012895 dilution Substances 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
239000000126 substance Substances 0.000 claims description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
241001124076 Aphididae Species 0.000 claims description 3
241000238631 Hexapoda Species 0.000 claims description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
238000002474 experimental method Methods 0.000 claims description 3
150000002367 halogens Chemical class 0.000 claims description 3
239000000575 pesticide Substances 0.000 claims description 3
239000011593 sulfur Substances 0.000 claims description 3
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 2
229920000742 Cotton Polymers 0.000 claims description 2
235000009161 Espostoa lanata Nutrition 0.000 claims description 2
240000001624 Espostoa lanata Species 0.000 claims description 2
206010061217 Infestation Diseases 0.000 claims description 2
240000007594 Oryza sativa Species 0.000 claims description 2
235000010627 Phaseolus vulgaris Nutrition 0.000 claims description 2
241001674048 Phthiraptera Species 0.000 claims description 2
235000002098 Vicia faba var. major Nutrition 0.000 claims description 2
238000004587 chromatography analysis Methods 0.000 claims description 2
235000005489 dwarf bean Nutrition 0.000 claims description 2
238000011156 evaluation Methods 0.000 claims description 2
239000011521 glass Substances 0.000 claims description 2
239000004033 plastic Substances 0.000 claims description 2
238000002360 preparation method Methods 0.000 claims description 2
239000004563 wettable powder Substances 0.000 claims description 2
230000001419 dependent effect Effects 0.000 claims 4
-1 -CH2CH=CHCl Chemical group 0.000 abstract description 4
229910052783 alkali metal Inorganic materials 0.000 abstract description 2
150000001340 alkali metals Chemical class 0.000 abstract description 2
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 description 5
239000002904 solvent Substances 0.000 description 4
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000000969 carrier Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
241000256244 Heliothis virescens Species 0.000 description 2
244000061176 Nicotiana tabacum Species 0.000 description 2
235000002637 Nicotiana tabacum Nutrition 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
241000256250 Spodoptera littoralis Species 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
241000607479 Yersinia pestis Species 0.000 description 2
239000002253 acid Substances 0.000 description 2
239000000654 additive Substances 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical class OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 2
238000009472 formulation Methods 0.000 description 2
239000002574 poison Substances 0.000 description 2
231100000614 poison Toxicity 0.000 description 2
239000000243 solution Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
125000006729 (C2-C5) alkenyl group Chemical group 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 1
241000254032 Acrididae Species 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
241000238888 Argasidae Species 0.000 description 1
241000238660 Blattidae Species 0.000 description 1
241000257161 Calliphoridae Species 0.000 description 1
241001414835 Cimicidae Species 0.000 description 1
241000255749 Coccinellidae Species 0.000 description 1
241000256113 Culicidae Species 0.000 description 1
241001466044 Delphacidae Species 0.000 description 1
241001414830 Diaspididae Species 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
241000238816 Gryllidae Species 0.000 description 1
241001243087 Gryllotalpidae Species 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
241000238889 Ixodidae Species 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
241000257226 Muscidae Species 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
241001415279 Pseudococcidae Species 0.000 description 1
241000258921 Pulicidae Species 0.000 description 1
241000255893 Pyralidae Species 0.000 description 1
241001510071 Pyrrhocoridae Species 0.000 description 1
241001124072 Reduviidae Species 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
241000255588 Tephritidae Species 0.000 description 1
241000896028 Tettigoniidae Species 0.000 description 1
241000131339 Tipulidae Species 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
125000003302 alkenyloxy group Chemical group 0.000 description 1
125000005108 alkenylthio group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000005083 alkoxyalkoxy group Chemical group 0.000 description 1
125000005210 alkyl ammonium group Chemical group 0.000 description 1
125000005133 alkynyloxy group Chemical group 0.000 description 1
125000005336 allyloxy group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
150000003857 carboxamides Chemical class 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
230000002045 lasting effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000000199 molecular distillation Methods 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
238000012545 processing Methods 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000002002 slurry Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
235000017550 sodium carbonate Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
125000000446 sulfanediyl group Chemical group *S* 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
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
150000003580 thiophosphoric acid esters Chemical class 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 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
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/18—Esters of thiophosphoric acids with hydroxyaryl compounds

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)

CH1604372A 1972-11-03 1972-11-03 Pesticidal phosphorothiolates and-thiolothionates - O-(m)ethyl-5-propyl or butyl-O-substd phenyl-phosphorothiolates and-thiolothionates are insecticides, acaracides and fungicides CH572308A5 (en)

Priority Applications (21)

Application Number	Priority Date	Filing Date	Title
CH1604372A CH572308A5 (en)	1972-11-03	1972-11-03	Pesticidal phosphorothiolates and-thiolothionates - O-(m)ethyl-5-propyl or butyl-O-substd phenyl-phosphorothiolates and-thiolothionates are insecticides, acaracides and fungicides
CA183,449A CA1058192A (fr)	1972-11-03	1973-10-16	Ethers
IL43458A IL43458A (en)	1972-11-03	1973-10-22	Esters of thiophosphoric and dithiophosphoric acids their manufacture and insecticidal and acaricidal compositions containing them
AU61705/73A AU480851B2 (en)	1972-11-03	1973-10-23	Pesticidal mono-and di-thiophosphate
NL7314564A NL7314564A (fr)	1972-11-03	1973-10-23
US408874A US3898305A (en)	1972-11-03	1973-10-23	O-methyl/ethyl-S-propyl/butyl-O-chloroallylphenyl thiophosphates and dithiophosphates
OA55050A OA04500A (fr)	1972-11-03	1973-10-30	Esters d'acides du phosphore et produits pesticides qui en contiennent.
DE19732354653 DE2354653A1 (de)	1972-11-03	1973-10-31	Neue ester
FR7338840A FR2205526B1 (fr)	1972-11-03	1973-10-31
BE137301A BE806794A (fr)	1972-11-03	1973-10-31	Esters d'acides du phosphore et produits pesticides qui en contiennent
EG414/73A EG11386A (en)	1972-11-03	1973-11-01	Thiophosphoric and dithiophosphoric acid esters
TR17851A TR17851A (tr)	1972-11-03	1973-11-01	Yeni esterler
AT924773A AT324772B (de)	1972-11-03	1973-11-02	Insektizides und akarizides mittel
JP48123910A JPS4975732A (fr)	1972-11-03	1973-11-02
GB5107073A GB1441639A (en)	1972-11-03	1973-11-02	Pesticidal mono- and di-thiophosphates
ZA738449A ZA738449B (en)	1972-11-03	1973-11-02	New esters
US05/534,594 US3943202A (en)	1972-11-03	1974-12-20	O-methyl/ethyl-s-propyl/butyl-o-phenyl thiophosphates and dithiophosphates having an ether group or the phenyl ring
US05/534,933 US3935233A (en)	1972-11-03	1974-12-20	O-methyl/ethyl-s-propyl/butyl-o-phenyl thiophosphates and dithiophosphates having an o-heterocyclic group or the phenyl ring
US05/534,591 US3991141A (en)	1972-11-03	1974-12-20	O-methyl/ethyl-S-propyl/butyl-O-phenyl thiphosphates and dithiophosphates having a thioether group on the phenyl ring
US05/578,960 US4017612A (en)	1972-11-03	1975-05-19	Combatting insects and acarids with certain O-methyl/ethyl-S-propyl/butyl-O-phenyl-thiophosphates and -dithiophosphates
US05/751,918 US4262012A (en)	1972-11-03	1976-12-17	O-Methyl/ethyl-s-propyl/butyl-o-phenyl thiophosphates and dithiophosphates having an s-heterocyclic group on the phenyl ring

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1604372A CH572308A5 (en)	1972-11-03	1972-11-03	Pesticidal phosphorothiolates and-thiolothionates - O-(m)ethyl-5-propyl or butyl-O-substd phenyl-phosphorothiolates and-thiolothionates are insecticides, acaracides and fungicides

Publications (1)

Publication Number	Publication Date
CH572308A5 true CH572308A5 (en)	1976-02-13

Family

ID=4414021

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1604372A CH572308A5 (en)	1972-11-03	1972-11-03	Pesticidal phosphorothiolates and-thiolothionates - O-(m)ethyl-5-propyl or butyl-O-substd phenyl-phosphorothiolates and-thiolothionates are insecticides, acaracides and fungicides

Country Status (4)

Country	Link
BE (1)	BE806794A (fr)
CH (1)	CH572308A5 (fr)
TR (1)	TR17851A (fr)
ZA (1)	ZA738449B (fr)

1972
- 1972-11-03 CH CH1604372A patent/CH572308A5/de not_active IP Right Cessation
1973
- 1973-10-31 BE BE137301A patent/BE806794A/fr unknown
- 1973-11-01 TR TR17851A patent/TR17851A/xx unknown
- 1973-11-02 ZA ZA738449A patent/ZA738449B/xx unknown

Also Published As

Publication number	Publication date
TR17851A (tr)	1976-05-12
BE806794A (fr)	1974-04-30
ZA738449B (en)	1974-09-25

Legal Events

Date	Code	Title	Description
1982-07-30	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DE2303185C2 (de)	1986-01-09	Thiophosphorsäurephenylester, Verfahren zu ihrer Herstellung sowie diese enthaltende Schädlingsbekämpfungsmittel
DE2411809A1 (de)	1974-09-26	Thiolphosphorsaeureester, verfahren zu ihrer herstellung und ihre verwendung
CH572308A5 (en)	1976-02-13	Pesticidal phosphorothiolates and-thiolothionates - O-(m)ethyl-5-propyl or butyl-O-substd phenyl-phosphorothiolates and-thiolothionates are insecticides, acaracides and fungicides
DE2304128C2 (de)	1982-05-06	Thiolphosphorsäureester, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung
DE2422324C2 (de)	1984-05-03	Diphenyläther-phosphorverbindungen, Verfahren zu ihrer Herstellung und diese enthaltende Schädlingsbekämpfungsmittel
DE2332162A1 (de)	1974-01-17	Neue ester
DE2354586A1 (de)	1974-05-16	Neue ester
CH570765A5 (en)	1975-12-31	Pyridyl (di)thiophosphates prepn - with biocidal activity
CH574712A5 (en)	1976-04-30	O-alkyl-s-alkyl-o-nitrophenyl thiophosphates - with pesticidal activity
DE2439663A1 (de)	1975-03-06	Diphenylaetherphosphate, verfahren zu ihrer herstellung und ihre verwendung
CH575211A5 (en)	1976-05-14	(di)thiophosphoric acid esters - with biocidal activity
CH581435A5 (en)	1976-11-15	Pesticidal 1,2,3-Triazol-4-yl-(thiono)phosph(on)ates - prepd. by reacting 4-hydroxy-1,2,4-triazoles with (thiono)phosphor(on)yl halides
CH570764A5 (en)	1975-12-31	Phosphoramidothiolic acid esters - insecticides, acaricides, nematocides, viricides, bactericides, fungicides and herbicides
CH571817A5 (en)	1976-01-30	Pesticidal 1,2,4-triazol-3-yl phosph(on)ates - e.g. O,O-diethyl-O-(1-methyl-5-(alpha-carbethoxybenzyl)-1,2,4-triazol-- 3-yl)-phosphate
CH623992A5 (en)	1981-07-15	A pesticide
CH574215A5 (en)	1976-04-15	0-(2-Alkenylphenyl) O,S-dialkyl thiophosphates - with insecticidal, acaricidal, fungicidal and nematocidal 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
DE2356453A1 (de)	1974-05-16	Alkylendithiophosphorsaeureester, verfahren zu ihrer herstellung und ihre verwendung
CH575717A5 (en)	1976-05-31	S-Arylthioalkyl-O,S-dialkyl dithiophosphates - with insecticidal, acaricidal, fungicidal, nematocidal activity, etc.
CH575210A5 (en)	1976-05-14	O-(1-aryl-2-halovinyl) (di)thiophosphates - insecticides acaricides and nematocides
CH549942A (de)	1974-06-14	Schaedlingsbekaempfungsmittel.
CH590007A5 (en)	1977-07-29	1-(2-Cyanoethyl)-1,2,4-triazol-3-yl (thio)phosph(on)ates - prepd. by reacting 3-hydroxy cpds. with (thio)phosphor(on)yl halides
CH580387A5 (en)	1976-10-15	Diphenylether phosphates as pesticides - from hydroxy diphenyl ethers and substd. phosphoric acid chlorides
DE2430758A1 (de)	1975-01-23	Oxadiazolylverbindungen, verfahren zu ihrer herstellung und ihre verwendung zur schaedlingsbekaempfung
CH588807A5 (en)	1977-06-15	N-Phenyl-N'-phenylthio-formamidine derivs - prepd. by reacting N-phenyl-formamidines with phenylsulphenyl halides