SE410184B - Forening till anvendning vid bekempning av insekter och arter av ordningen akarina - Google Patents
Forening till anvendning vid bekempning av insekter och arter av ordningen akarinaInfo
- Publication number
- SE410184B SE410184B SE7301031A SE7301031A SE410184B SE 410184 B SE410184 B SE 410184B SE 7301031 A SE7301031 A SE 7301031A SE 7301031 A SE7301031 A SE 7301031A SE 410184 B SE410184 B SE 410184B
- Authority
- SE
- Sweden
- Prior art keywords
- methyl
- phenoxy
- benzene
- oxy
- dimethyl
- Prior art date
Links
- 241000238631 Hexapoda Species 0.000 title claims description 7
- 241000894007 species Species 0.000 title claims description 4
- -1 methoxy ethoxy, vinyl Chemical group 0.000 claims description 63
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 60
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 23
- 239000000460 chlorine Substances 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 229910052801 chlorine Inorganic materials 0.000 claims description 11
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 10
- 239000004593 Epoxy Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 150000002431 hydrogen Chemical class 0.000 claims description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 150000001721 carbon Chemical group 0.000 claims description 2
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims 1
- 239000013543 active substance Substances 0.000 description 44
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 38
- 239000000243 solution Substances 0.000 description 34
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 30
- 239000002904 solvent Substances 0.000 description 25
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 19
- 239000000203 mixture Substances 0.000 description 18
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- ZSBDGXGICLIJGD-UHFFFAOYSA-N 4-phenoxyphenol Chemical compound C1=CC(O)=CC=C1OC1=CC=CC=C1 ZSBDGXGICLIJGD-UHFFFAOYSA-N 0.000 description 12
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
- 239000003513 alkali Substances 0.000 description 12
- 239000000843 powder Substances 0.000 description 12
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- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 9
- 241001465754 Metazoa Species 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 9
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- 150000004820 halides Chemical class 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 8
- 229910019142 PO4 Inorganic materials 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 8
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- 238000002360 preparation method Methods 0.000 description 8
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- 239000000654 additive Substances 0.000 description 7
- 239000000969 carrier Substances 0.000 description 7
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
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- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000012433 hydrogen halide Substances 0.000 description 6
- 229910000039 hydrogen halide Inorganic materials 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 description 6
- 239000000741 silica gel Substances 0.000 description 6
- 229910002027 silica gel Inorganic materials 0.000 description 6
- 229910052938 sodium sulfate Inorganic materials 0.000 description 6
- 235000011152 sodium sulphate Nutrition 0.000 description 6
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 5
- 239000005995 Aluminium silicate Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
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- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 5
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- 239000010695 polyglycol Substances 0.000 description 5
- 238000012958 reprocessing Methods 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 4
- 241001127120 Dysdercus fasciatus Species 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 235000011941 Tilia x europaea Nutrition 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
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- 239000006185 dispersion Substances 0.000 description 4
- 239000003480 eluent Substances 0.000 description 4
- ZKQFHRVKCYFVCN-UHFFFAOYSA-N ethoxyethane;hexane Chemical compound CCOCC.CCCCCC ZKQFHRVKCYFVCN-UHFFFAOYSA-N 0.000 description 4
- 150000002191 fatty alcohols Chemical class 0.000 description 4
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 4
- 239000004571 lime Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 4
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- 238000003756 stirring Methods 0.000 description 4
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- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
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- 150000001298 alcohols Chemical class 0.000 description 3
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- 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 2
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- 125000000913 palmityl 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])[H] 0.000 description 2
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- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 2
- SCWKRWCUMCMVPW-UHFFFAOYSA-N phenyl n-methylcarbamate Chemical compound CNC(=O)OC1=CC=CC=C1 SCWKRWCUMCMVPW-UHFFFAOYSA-N 0.000 description 2
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- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
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- OPASCBHCTNRLRM-UHFFFAOYSA-N thiometon Chemical compound CCSCCSP(=S)(OC)OC OPASCBHCTNRLRM-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 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
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
- C07D303/20—Ethers with hydroxy compounds containing no oxirane rings
- C07D303/24—Ethers with hydroxy compounds containing no oxirane rings with polyhydroxy compounds
-
- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
- A01N31/16—Oxygen or sulfur directly attached to an aromatic ring system with two or more oxygen or sulfur atoms directly attached to the same aromatic ring system
-
- 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
- A01N39/00—Biocides, pest repellants or attractants, or plant growth regulators containing aryloxy- or arylthio-aliphatic or cycloaliphatic compounds, containing the group or, e.g. phenoxyethylamine, phenylthio-acetonitrile, phenoxyacetone
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/257—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings
- C07C43/263—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings the aromatic rings being non-condensed
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Epoxy Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH169572A CH568714A5 (en) | 1972-02-04 | 1972-02-04 | Pesticidal subst hydrocarbyl ethers - with effects on insects and acarina |
| CH224072A CH582473A5 (en) | 1972-02-16 | 1972-02-16 | Pesticidal subst hydrocarbyl ethers - with effects on insects and acarina |
| CH4873A CH584511A5 (en) | 1973-01-03 | 1973-01-03 | Pesticidal subst hydrocarbyl ethers - with effects on insects and acarina |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SE410184B true SE410184B (sv) | 1979-10-01 |
Family
ID=27171733
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE7301031A SE410184B (sv) | 1972-02-04 | 1973-01-25 | Forening till anvendning vid bekempning av insekter och arter av ordningen akarina |
| SE7801241A SE7801241L (sv) | 1972-02-04 | 1978-02-02 | Etrar |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE7801241A SE7801241L (sv) | 1972-02-04 | 1978-02-02 | Etrar |
Country Status (16)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1984004298A1 (en) * | 1983-04-25 | 1984-11-08 | Cheminova As | Arylcycloalkyl ether derivatives, their use and preparation |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3998972A (en) * | 1974-10-14 | 1976-12-21 | Ciba-Geigy Corporation | Diphenyl derivatives |
| GB1570982A (en) * | 1976-03-05 | 1980-07-09 | Shell Int Research | Substituted benzyl ethers and thioethers |
| CH624087A5 (en) * | 1976-08-25 | 1981-07-15 | Hoechst Ag | Process for the preparation of phenoxyphenoxypropionic acid derivatives |
| FR2434133B1 (fr) * | 1978-06-21 | 1988-04-29 | Montedison Spa | Nouveaux diethers hydroquinoniques dotes d'une activite hormonale juvenile et acaricide |
| CH643223A5 (it) * | 1978-06-21 | 1984-05-30 | Montedison Spa | Dieteri idrochinonici aventi attivita ormonica giovanile e acaricida. |
| US4408076A (en) * | 1981-06-05 | 1983-10-04 | Zoecon Corporation | Phenoxy unsaturated carboxylic acid esters and derivatives |
| US4525205A (en) * | 1982-01-22 | 1985-06-25 | Zoecon Corporation | Herbicidal compositions comprising compounds containing a phenylaminophenoxy moiety |
| US4429167A (en) | 1981-09-04 | 1984-01-31 | Zoecon Corporation | 3-Alkoxy-4-substituted-phenoxy-2,3-unsaturated acids, esters and derivatives |
| US4529438A (en) * | 1982-03-23 | 1985-07-16 | Zoecon Corp. | Pyridyloxy-phenoxy-alkanoic acid esters and derivatives |
| ES2054081T3 (es) * | 1988-09-15 | 1994-08-01 | Ciba Geigy Ag | Nuevos eteres. |
| TW306864B (enrdf_load_stackoverflow) * | 1993-10-19 | 1997-06-01 | Sumitomo Chemical Co | |
| US5398115A (en) * | 1994-02-24 | 1995-03-14 | Lin; Iyh-Han | Facsimile communication for locating and transmitting information from a document to selective call receivers |
| DE69505490T2 (de) * | 1994-08-04 | 1999-06-24 | Sumitomo Chemical Co., Ltd., Osaka | Dihalopropenverbindungen, sie enthaltende insektizide/akarizide mittel, und zwischenprodukte |
| TW307746B (enrdf_load_stackoverflow) * | 1994-10-14 | 1997-06-11 | Sumitomo Chemical Co | |
| WO1996015093A1 (fr) * | 1994-11-14 | 1996-05-23 | Sumitomo Chemical Company, Limited | Composes dihalopropene, leur utilisation et intermediaires utilises pour leur production |
| DE69610204T2 (de) * | 1995-04-18 | 2001-05-03 | Sumitomo Chemical Co., Ltd. | Dihalopropen-verbindungen, diese enthaltende insektizide und intermediate zu ihrer herstellung |
| US5869506A (en) * | 1996-01-31 | 1999-02-09 | Sumitomo Chemical Company, Limited | Fluoropropene compound, an insecticide containing the same and an intermediate for production thereof |
| JP4982950B2 (ja) * | 2004-02-05 | 2012-07-25 | 住友化学株式会社 | ピラゾール化合物とその製造中間体、ならびにその有害節足動物防除用途 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3155733A (en) * | 1962-06-27 | 1964-11-03 | Dow Chemical Co | Aryloxyarylthioalkenyl ethers |
| CH526258A (de) * | 1970-03-25 | 1972-08-15 | Hoffmann La Roche | Schädlingsbekämpfungsmittel |
| ZA712229B (en) * | 1970-04-17 | 1971-12-29 | Hoffmann La Roche | Phenyloxy derivatives |
-
0
- BE BE794894D patent/BE794894A/xx unknown
-
1973
- 1973-01-23 FI FI173/73A patent/FI59389C/fi active
- 1973-01-25 SE SE7301031A patent/SE410184B/sv unknown
- 1973-01-29 IL IL41419A patent/IL41419A/xx unknown
- 1973-01-31 SU SU731880508A patent/SU719479A3/ru active
- 1973-01-31 CA CA162,523A patent/CA1045144A/en not_active Expired
- 1973-01-31 NL NL7301400A patent/NL7301400A/xx not_active Application Discontinuation
- 1973-02-01 DE DE2304962A patent/DE2304962C2/de not_active Expired
- 1973-02-02 GB GB538573A patent/GB1424211A/en not_active Expired
- 1973-02-02 FR FR7303688A patent/FR2168115B1/fr not_active Expired
- 1973-02-02 IT IT19996/73A patent/IT986958B/it active
- 1973-02-02 DD DD168632A patent/DD107383A5/xx unknown
- 1973-02-02 HU HUCI1335A patent/HU165797B/hu not_active IP Right Cessation
- 1973-02-02 AT AT94573A patent/AT322279B/de not_active IP Right Cessation
- 1973-02-03 JP JP48014204A patent/JPS5844649B2/ja not_active Expired
- 1973-02-03 EG EG43/73A patent/EG10996A/xx active
-
1978
- 1978-02-02 SE SE7801241A patent/SE7801241L/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1984004298A1 (en) * | 1983-04-25 | 1984-11-08 | Cheminova As | Arylcycloalkyl ether derivatives, their use and preparation |
Also Published As
| Publication number | Publication date |
|---|---|
| EG10996A (en) | 1976-09-30 |
| SE7801241L (sv) | 1978-02-02 |
| FR2168115A1 (enrdf_load_stackoverflow) | 1973-08-24 |
| IL41419A (en) | 1978-08-31 |
| FI59389C (fi) | 1981-08-10 |
| DE2304962C2 (de) | 1984-12-13 |
| AT322279B (de) | 1975-05-12 |
| BE794894A (fr) | 1973-08-02 |
| JPS4886835A (enrdf_load_stackoverflow) | 1973-11-15 |
| FR2168115B1 (enrdf_load_stackoverflow) | 1978-04-21 |
| JPS5844649B2 (ja) | 1983-10-04 |
| CA1045144A (en) | 1978-12-26 |
| HU165797B (enrdf_load_stackoverflow) | 1974-11-28 |
| DE2304962A1 (de) | 1973-08-09 |
| SU719479A3 (ru) | 1980-02-29 |
| IL41419A0 (en) | 1973-03-30 |
| DD107383A5 (enrdf_load_stackoverflow) | 1974-08-05 |
| IT986958B (it) | 1975-01-30 |
| GB1424211A (en) | 1976-02-11 |
| NL7301400A (enrdf_load_stackoverflow) | 1973-08-07 |
| FI59389B (fi) | 1981-04-30 |
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