DE2423683C2 - 0-Triazolyl(thiono)-phosphor(phosphon)säureester und -esteramide, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide, Akarizide und Nematizide - Google Patents
0-Triazolyl(thiono)-phosphor(phosphon)säureester und -esteramide, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide, Akarizide und NematizideInfo
- Publication number
- DE2423683C2 DE2423683C2 DE2423683A DE2423683A DE2423683C2 DE 2423683 C2 DE2423683 C2 DE 2423683C2 DE 2423683 A DE2423683 A DE 2423683A DE 2423683 A DE2423683 A DE 2423683A DE 2423683 C2 DE2423683 C2 DE 2423683C2
- Authority
- DE
- Germany
- Prior art keywords
- phosphonic
- acid esters
- phosphorus
- thiono
- triazolyl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
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- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical class ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 241000201423 Xiphinema Species 0.000 description 1
- 241001466337 Yponomeuta Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 244000000054 animal parasite Species 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 235000015241 bacon Nutrition 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 244000309466 calf Species 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 208000031513 cyst Diseases 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 244000078703 ectoparasite Species 0.000 description 1
- KYFDJVWOXDDUBT-UHFFFAOYSA-N ethoxy methyl hydrogen phosphate Chemical compound CCOOP(O)(=O)OC KYFDJVWOXDDUBT-UHFFFAOYSA-N 0.000 description 1
- YJCXKNNURGCXFQ-UHFFFAOYSA-N ethoxy(ethyl)phosphinic acid Chemical compound CCOP(O)(=O)CC YJCXKNNURGCXFQ-UHFFFAOYSA-N 0.000 description 1
- OJZGWRZUOHSWMB-UHFFFAOYSA-N ethoxy-dihydroxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(O)(O)=S OJZGWRZUOHSWMB-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 235000020044 madeira Nutrition 0.000 description 1
- 201000004792 malaria Diseases 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- SYBYTAAJFKOIEJ-UHFFFAOYSA-N methyl iso-propyl ketone Natural products CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 210000003205 muscle Anatomy 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical compound CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- UTVCBQCZOQNCAY-UHFFFAOYSA-N scleramide Natural products O=C1NCC(=O)NC(CC=2C=CC=CC=2)C(=O)N(C)C(CC=2C=CC=CC=2)C(=O)NCC(=O)NC(CCC(N)=O)C(=O)N(C)C1CC1=CC=CC=C1 UTVCBQCZOQNCAY-UHFFFAOYSA-N 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms
-
- 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
- C07F9/6518—Five-membered rings
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)
Priority Applications (23)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2423683A DE2423683C2 (de) | 1974-05-15 | 1974-05-15 | 0-Triazolyl(thiono)-phosphor(phosphon)säureester und -esteramide, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide, Akarizide und Nematizide |
AR258790A AR206145A1 (es) | 1974-05-15 | 1975-01-01 | Nuevos esteres de acidos o - triazol - (3) - il - (1, 2, 4) - fosforicos -tionofosforicos -fosfonicos y -tionofosfonicos y amidas de esteres de acidos fosforicos y -tionosfosforicos de propiedades insecticidas composiciones insecticidas acaricidas y nematocidas a base de los mismos y procedimiento para la produccion de dichos compuestos |
GB17288/75A GB1494663A (en) | 1974-05-15 | 1975-04-25 | O-triazolyl(thiono)-phosphoric(phosphonic)acid esters and ester-amides process for their preparation and their use as insecticides acaricides or nematocides |
US05/576,074 US3987168A (en) | 1974-05-15 | 1975-05-09 | O-Alkyl-O-[1-cyanoalkyl-5-substituted-mercapto-triazol(3)yl]-(thiono)-phosphoric(phosphonic) acid esters or ester-amides |
IL7547271A IL47271A (en) | 1974-05-15 | 1975-05-12 | O-triazolyl(thiono)-phosphoric(phosphonic)acid esters and esteramides their preparation and insecticidal acaricidal and nematicidal compositions containing them |
NL7505607A NL7505607A (nl) | 1974-05-15 | 1975-05-13 | Werkwijze voor het bereiden van o-triazolyl(thi- ono)-fosfor(fosfon)-zuuresters respectievelijk - -esteramiden, werkwijze voor het bereiden van preparaten met insecticide, acaricide en/of ne- maticide werking alsmede gevormde preparaten. |
RO7582228A RO66235A (ro) | 1974-05-15 | 1975-05-13 | Procedeu de obtinere a esterilor acizilor o-triazolil fosforic,(tionofosforic),fosfonic,(tionofosfonic) |
AT365575A AT331262B (de) | 1974-05-15 | 1975-05-13 | Verfahren zur herstellung von neuen o-triazolyl- (thiono) -phosphor (phosphon)-saureestern bzw. -esteramiden |
DD186004A DD118982A5 (en, 2012) | 1974-05-15 | 1975-05-13 | |
IT23287/75A IT1038085B (it) | 1974-05-15 | 1975-05-13 | Esteri oppure esteri amidi o tria zolil tion fosforici fosforinci procedimento per la loro prepara ziono e loro impiego come insetti cidi acaricidi e nematocidi |
CH615175A CH611313A5 (en, 2012) | 1974-05-15 | 1975-05-13 | |
JP50055547A JPS5811404B2 (ja) | 1974-05-15 | 1975-05-13 | 殺虫、殺ダニおよび殺線虫剤 |
JP5554675A JPS5735839B2 (en, 2012) | 1974-05-15 | 1975-05-13 | |
LU72463A LU72463A1 (en, 2012) | 1974-05-15 | 1975-05-13 | |
AU81162/75A AU8116275A (en) | 1974-05-15 | 1975-05-14 | D-triazolyl%thiono<-phosphoric%phosphonic<acid esters |
ES437694A ES437694A1 (es) | 1974-05-15 | 1975-05-14 | Procedimiento para preparar esteres y amidas de esteres de acidos o-triazolil(tiono)-fosforicos (fosfonicos). |
TR18170A TR18170A (tr) | 1974-05-15 | 1975-05-14 | O-triazolil (tiono)-fosforik (fosfonik) asit esterleri ve ester amidleri, bunlarin hazirlanisi icin usul ve bunlarin ensektisideler ve nematosidler olarak kullanilmalari |
BR2995/74D BR7502995A (pt) | 1974-05-15 | 1975-05-14 | Processo para a preparacao de esteres e amidas de aperfeicoamentos relativos a maquina de folhear maesteres o-triazolilicos de acido (tiono)-fosforicodeira (fosfonico) e composicoes inseticidas a base destes |
BE156331A BE829053A (fr) | 1974-05-15 | 1975-05-14 | Nouveaux esters et amides d'esters de 0-triazolyle d'acide (thiono) phosphorique (phosphonique), leur procede de preparation et leur application comme insecticides, acaricides et nematicides |
DK211675A DK136530C (da) | 1974-05-15 | 1975-05-14 | Insecticidt,acaricidt og nematodicidt virksomme 0-triazolyl(thiono)-phosphor(phosphon)-syreestere eller-esteramider |
ZA00753123A ZA753123B (en) | 1974-05-15 | 1975-05-14 | O - triazolyl (thiono) - phosphoric (phosphoric) acid esters and ester-amides, process for their preparation and their use as insecticides, acaricides or nematocides |
FR7515249A FR2271230B1 (en, 2012) | 1974-05-15 | 1975-05-15 | |
KE2846A KE2846A (en) | 1974-05-15 | 1978-06-13 | O-triazolyl (thino)-phosphoric(phosphonic) acid esters and ester-amides, process for their preparation and their use as insecticides, acaricides or nematocides |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2423683A DE2423683C2 (de) | 1974-05-15 | 1974-05-15 | 0-Triazolyl(thiono)-phosphor(phosphon)säureester und -esteramide, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide, Akarizide und Nematizide |
Publications (2)
Publication Number | Publication Date |
---|---|
DE2423683A1 DE2423683A1 (de) | 1975-11-27 |
DE2423683C2 true DE2423683C2 (de) | 1982-10-21 |
Family
ID=5915673
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE2423683A Expired DE2423683C2 (de) | 1974-05-15 | 1974-05-15 | 0-Triazolyl(thiono)-phosphor(phosphon)säureester und -esteramide, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide, Akarizide und Nematizide |
Country Status (22)
Country | Link |
---|---|
US (1) | US3987168A (en, 2012) |
JP (2) | JPS5735839B2 (en, 2012) |
AR (1) | AR206145A1 (en, 2012) |
AT (1) | AT331262B (en, 2012) |
AU (1) | AU8116275A (en, 2012) |
BE (1) | BE829053A (en, 2012) |
BR (1) | BR7502995A (en, 2012) |
CH (1) | CH611313A5 (en, 2012) |
DD (1) | DD118982A5 (en, 2012) |
DE (1) | DE2423683C2 (en, 2012) |
DK (1) | DK136530C (en, 2012) |
ES (1) | ES437694A1 (en, 2012) |
FR (1) | FR2271230B1 (en, 2012) |
GB (1) | GB1494663A (en, 2012) |
IL (1) | IL47271A (en, 2012) |
IT (1) | IT1038085B (en, 2012) |
KE (1) | KE2846A (en, 2012) |
LU (1) | LU72463A1 (en, 2012) |
NL (1) | NL7505607A (en, 2012) |
RO (1) | RO66235A (en, 2012) |
TR (1) | TR18170A (en, 2012) |
ZA (1) | ZA753123B (en, 2012) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2301400C2 (de) * | 1973-01-12 | 1984-12-13 | Bayer Ag, 5090 Leverkusen | 0-Triazolyl-thionophosphor(phosphon)-säureester und -esteramide, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Akarizide |
SE7513987L (sv) * | 1975-12-11 | 1977-06-12 | Paul Goran Sigvard Lindroos | Sett att behandla vetskor innehallande blodsubstanser |
JPS58174243A (ja) * | 1982-04-05 | 1983-10-13 | 株式会社大竹製作所 | 脱ぷ機の構造 |
JPS6067708U (ja) * | 1983-10-14 | 1985-05-14 | 九州日立マクセル株式会社 | ヘア−ドライヤ |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2301400C2 (de) * | 1973-01-12 | 1984-12-13 | Bayer Ag, 5090 Leverkusen | 0-Triazolyl-thionophosphor(phosphon)-säureester und -esteramide, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide und Akarizide |
US4172080A (en) * | 1973-12-06 | 1979-10-23 | Ciba-Geigy Corporation | Phosphorus esters of 1-cyanoethyl-1,2,4-triazol-3-ols |
-
1974
- 1974-05-15 DE DE2423683A patent/DE2423683C2/de not_active Expired
-
1975
- 1975-01-01 AR AR258790A patent/AR206145A1/es active
- 1975-04-25 GB GB17288/75A patent/GB1494663A/en not_active Expired
- 1975-05-09 US US05/576,074 patent/US3987168A/en not_active Expired - Lifetime
- 1975-05-12 IL IL7547271A patent/IL47271A/xx unknown
- 1975-05-13 LU LU72463A patent/LU72463A1/xx unknown
- 1975-05-13 AT AT365575A patent/AT331262B/de not_active IP Right Cessation
- 1975-05-13 IT IT23287/75A patent/IT1038085B/it active
- 1975-05-13 JP JP5554675A patent/JPS5735839B2/ja not_active Expired
- 1975-05-13 JP JP50055547A patent/JPS5811404B2/ja not_active Expired
- 1975-05-13 RO RO7582228A patent/RO66235A/ro unknown
- 1975-05-13 CH CH615175A patent/CH611313A5/xx not_active IP Right Cessation
- 1975-05-13 NL NL7505607A patent/NL7505607A/xx not_active Application Discontinuation
- 1975-05-13 DD DD186004A patent/DD118982A5/xx unknown
- 1975-05-14 BR BR2995/74D patent/BR7502995A/pt unknown
- 1975-05-14 DK DK211675A patent/DK136530C/da active
- 1975-05-14 TR TR18170A patent/TR18170A/xx unknown
- 1975-05-14 ZA ZA00753123A patent/ZA753123B/xx unknown
- 1975-05-14 ES ES437694A patent/ES437694A1/es not_active Expired
- 1975-05-14 AU AU81162/75A patent/AU8116275A/en not_active Expired
- 1975-05-14 BE BE156331A patent/BE829053A/xx unknown
- 1975-05-15 FR FR7515249A patent/FR2271230B1/fr not_active Expired
-
1978
- 1978-06-13 KE KE2846A patent/KE2846A/xx unknown
Non-Patent Citations (1)
Title |
---|
NICHTS-ERMITTELT |
Also Published As
Publication number | Publication date |
---|---|
US3987168A (en) | 1976-10-19 |
BE829053A (fr) | 1975-11-14 |
JPS5735839B2 (en, 2012) | 1982-07-31 |
IL47271A0 (en) | 1975-07-28 |
DK211675A (da) | 1975-11-16 |
FR2271230A1 (en, 2012) | 1975-12-12 |
KE2846A (en) | 1978-06-30 |
IL47271A (en) | 1977-07-31 |
AR206145A1 (es) | 1976-06-30 |
ES437694A1 (es) | 1977-01-16 |
FR2271230B1 (en, 2012) | 1979-04-13 |
DK136530C (da) | 1978-05-16 |
BR7502995A (pt) | 1976-03-23 |
DE2423683A1 (de) | 1975-11-27 |
JPS50155629A (en, 2012) | 1975-12-16 |
LU72463A1 (en, 2012) | 1976-03-17 |
ZA753123B (en) | 1976-04-28 |
DD118982A5 (en, 2012) | 1976-04-05 |
CH611313A5 (en, 2012) | 1979-05-31 |
TR18170A (tr) | 1976-11-01 |
IT1038085B (it) | 1979-11-20 |
AU8116275A (en) | 1976-11-18 |
RO66235A (ro) | 1981-06-26 |
JPS5811404B2 (ja) | 1983-03-02 |
JPS50154254A (en, 2012) | 1975-12-12 |
DK136530B (da) | 1977-10-24 |
AT331262B (de) | 1976-08-10 |
NL7505607A (nl) | 1975-11-18 |
ATA365575A (de) | 1975-11-15 |
GB1494663A (en) | 1977-12-07 |
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