CS199651B2 - Fungicide - Google Patents
Fungicide Download PDFInfo
- Publication number
- CS199651B2 CS199651B2 CS76580A CS58076A CS199651B2 CS 199651 B2 CS199651 B2 CS 199651B2 CS 76580 A CS76580 A CS 76580A CS 58076 A CS58076 A CS 58076A CS 199651 B2 CS199651 B2 CS 199651B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- dimethyl
- methylsulfate
- iodide
- diphenylpyrazolium
- methyl
- Prior art date
Links
- 230000000855 fungicidal effect Effects 0.000 title claims description 3
- 239000000417 fungicide Substances 0.000 title abstract description 4
- -1 ethyl carboxymethyl Chemical group 0.000 claims abstract description 48
- 150000001875 compounds Chemical class 0.000 claims abstract description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
- 239000001257 hydrogen Substances 0.000 claims abstract description 6
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- XQEMNBNCQVQXMO-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 XQEMNBNCQVQXMO-UHFFFAOYSA-M 0.000 claims abstract description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims abstract description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 4
- 150000002367 halogens Chemical class 0.000 claims abstract description 4
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 3
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 claims abstract description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 21
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 16
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims description 14
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 9
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 9
- JEOVEEPACZXTPL-UHFFFAOYSA-N 1h-pyrazol-1-ium;perchlorate Chemical compound C1=CN[NH+]=C1.[O-]Cl(=O)(=O)=O JEOVEEPACZXTPL-UHFFFAOYSA-N 0.000 claims description 8
- JIJBWYXJIKAYLT-UHFFFAOYSA-N 1h-pyrazol-1-ium;iodide Chemical compound [I-].C1=CN[NH+]=C1 JIJBWYXJIKAYLT-UHFFFAOYSA-N 0.000 claims description 7
- 239000004480 active ingredient Substances 0.000 claims description 7
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 5
- ICIHDUSPYJNBRL-UHFFFAOYSA-N methyl sulfate;1h-pyrazol-1-ium Chemical compound [NH2+]1C=CC=N1.COS([O-])(=O)=O ICIHDUSPYJNBRL-UHFFFAOYSA-N 0.000 claims description 5
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 5
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims description 4
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
- LLIOTGIXSUTUJW-UHFFFAOYSA-K 1,2-dimethyl-3,5-diphenylpyrazol-1-ium phosphate Chemical compound P(=O)([O-])([O-])[O-].C[N+]=1N(C(=CC1C1=CC=CC=C1)C1=CC=CC=C1)C.C[N+]=1N(C(=CC1C1=CC=CC=C1)C1=CC=CC=C1)C.C[N+]=1N(C(=CC1C1=CC=CC=C1)C1=CC=CC=C1)C LLIOTGIXSUTUJW-UHFFFAOYSA-K 0.000 claims description 3
- MTCQFVYEKGHUGI-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;4-methylbenzenesulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 MTCQFVYEKGHUGI-UHFFFAOYSA-M 0.000 claims description 3
- VTWNZNWFJUMAOD-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 VTWNZNWFJUMAOD-UHFFFAOYSA-M 0.000 claims description 3
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- 229910002651 NO3 Inorganic materials 0.000 claims description 3
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 claims description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 2
- QPHPWHYLXYFPHZ-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;bromide Chemical compound [Br-].C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 QPHPWHYLXYFPHZ-UHFFFAOYSA-M 0.000 claims description 2
- QTVMXZDRWOUJRU-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;chloride Chemical compound [Cl-].C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 QTVMXZDRWOUJRU-UHFFFAOYSA-M 0.000 claims description 2
- BGCSXGXXLDPSHB-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;hydroxide Chemical compound [OH-].C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 BGCSXGXXLDPSHB-UHFFFAOYSA-M 0.000 claims description 2
- TWUBOZYAXNVYGS-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;iodide Chemical compound [I-].C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 TWUBOZYAXNVYGS-UHFFFAOYSA-M 0.000 claims description 2
- KJBWGQAKZBGIID-UHFFFAOYSA-M 1,2-dimethyl-3-(3-methylphenyl)-5-phenylpyrazol-2-ium iodide Chemical compound [I-].C[N+]=1N(C(=CC1C=1C=C(C=CC1)C)C1=CC=CC=C1)C KJBWGQAKZBGIID-UHFFFAOYSA-M 0.000 claims description 2
- UEUKEEVVFFCMTQ-UHFFFAOYSA-M 3,5-bis(3-chlorophenyl)-1,2-dimethylpyrazol-1-ium methyl sulfate Chemical compound COS([O-])(=O)=O.CN1[C+](C=C(N1C)C1=CC(Cl)=CC=C1)C1=CC(Cl)=CC=C1 UEUKEEVVFFCMTQ-UHFFFAOYSA-M 0.000 claims description 2
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 2
- JCKSULMEQCDNCW-UHFFFAOYSA-M Cl(=O)(=O)(=O)[O-].C[N+]=1N(C(=CC1C1=C(C=CC=C1)C)C1=CC=C(C=C1)C)C Chemical compound Cl(=O)(=O)(=O)[O-].C[N+]=1N(C(=CC1C1=C(C=CC=C1)C)C1=CC=C(C=C1)C)C JCKSULMEQCDNCW-UHFFFAOYSA-M 0.000 claims description 2
- XXLXQZYEZVWCMV-UHFFFAOYSA-M Cl(=O)(=O)(=O)[O-].ClC1=CC=C(C=C1)C=1N([N+](=C(C1)C1=CC=C(C=C1)Cl)C)C Chemical compound Cl(=O)(=O)(=O)[O-].ClC1=CC=C(C=C1)C=1N([N+](=C(C1)C1=CC=C(C=C1)Cl)C)C XXLXQZYEZVWCMV-UHFFFAOYSA-M 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- NGMPDONLQCPUOU-UHFFFAOYSA-M S(=O)(=O)(OC)[O-].C[N+]=1N(C(=CC1C1=CC=C(C=C1)C)C1=CC=C(C=C1)C)C Chemical compound S(=O)(=O)(OC)[O-].C[N+]=1N(C(=CC1C1=CC=C(C=C1)C)C1=CC=C(C=C1)C)C NGMPDONLQCPUOU-UHFFFAOYSA-M 0.000 claims description 2
- GZGOLPHEPJRRGJ-UHFFFAOYSA-M S(=O)(=O)(OC)[O-].ClC1=C(C=C(C=C1)Cl)C=1C=C(N([N+]1C)C)C1=CC=CC=C1 Chemical compound S(=O)(=O)(OC)[O-].ClC1=C(C=C(C=C1)Cl)C=1C=C(N([N+]1C)C)C1=CC=CC=C1 GZGOLPHEPJRRGJ-UHFFFAOYSA-M 0.000 claims description 2
- 239000013543 active substance Substances 0.000 claims description 2
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 claims description 2
- 229940077388 benzenesulfonate Drugs 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- 230000008018 melting Effects 0.000 claims 3
- 238000002844 melting Methods 0.000 claims 3
- MGSJXXVDLDJDBE-UHFFFAOYSA-M 1,2-dimethyl-3,5-bis(4-methylphenyl)pyrazol-1-ium 4-methylbenzenesulfonate Chemical compound C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C[N+]=1N(C(=CC1C1=CC=C(C=C1)C)C1=CC=C(C=C1)C)C MGSJXXVDLDJDBE-UHFFFAOYSA-M 0.000 claims 1
- LSPWBCMNEQSDEI-UHFFFAOYSA-N 1,2-dimethyl-3,5-diphenylpyrazol-1-ium nitrate Chemical compound [N+](=O)([O-])[O-].C[N+]=1N(C(=CC1C1=CC=CC=C1)C1=CC=CC=C1)C LSPWBCMNEQSDEI-UHFFFAOYSA-N 0.000 claims 1
- KPKVEKQHMRDJSA-UHFFFAOYSA-M 1,2-dimethyl-3-(2-methylphenyl)-5-(4-methylphenyl)pyrazol-1-ium iodide Chemical compound [I-].C[N+]=1N(C(=CC1C1=C(C=CC=C1)C)C1=CC=C(C=C1)C)C KPKVEKQHMRDJSA-UHFFFAOYSA-M 0.000 claims 1
- JADMQIUABBVKBV-UHFFFAOYSA-N 1,2-dimethyl-3-(3-methylphenyl)-5-(4-methylphenyl)pyrazol-2-ium Chemical compound C[N+]=1N(C(=CC1C1=CC=C(C=C1)C)C=1C=C(C=CC1)C)C JADMQIUABBVKBV-UHFFFAOYSA-N 0.000 claims 1
- ASLUVPLUYLXSPY-UHFFFAOYSA-M 1,2-dimethyl-3-(3-methylphenyl)-5-(4-methylphenyl)pyrazol-2-ium methyl sulfate Chemical compound S(=O)(=O)(OC)[O-].C[N+]=1N(C(=CC1C1=CC=C(C=C1)C)C=1C=C(C=CC1)C)C ASLUVPLUYLXSPY-UHFFFAOYSA-M 0.000 claims 1
- UAQGHXOBZKZFHU-UHFFFAOYSA-M 3,5-bis(3-fluorophenyl)-1,2-dimethylpyrazol-1-ium methyl sulfate Chemical compound S(=O)(=O)(OC)[O-].FC=1C=C(C=CC1)C=1N([N+](=C(C1)C1=CC(=CC=C1)F)C)C UAQGHXOBZKZFHU-UHFFFAOYSA-M 0.000 claims 1
- ZIQUOBUWCBBSTH-UHFFFAOYSA-M 3-(2,5-dimethylphenyl)-1,2-dimethyl-5-phenylpyrazol-1-ium perchlorate Chemical compound Cl(=O)(=O)(=O)[O-].C[N+]=1N(C(=CC1C1=C(C=CC(=C1)C)C)C1=CC=CC=C1)C ZIQUOBUWCBBSTH-UHFFFAOYSA-M 0.000 claims 1
- MCGVAQMAZQRCGY-UHFFFAOYSA-M 3-(2-fluorophenyl)-1,2-dimethyl-5-phenylpyrazol-1-ium methyl sulfate Chemical compound S(=O)(=O)(OC)[O-].FC1=C(C=CC=C1)C=1N([N+](=C(C1)C1=CC=CC=C1)C)C MCGVAQMAZQRCGY-UHFFFAOYSA-M 0.000 claims 1
- WRDCSPNUSXMKGF-UHFFFAOYSA-M 3-(3-iodophenyl)-1,2-dimethyl-5-phenylpyrazol-2-ium iodide Chemical compound [I-].IC=1C=C(C=CC1)C=1C=C(N([N+]1C)C)C1=CC=CC=C1 WRDCSPNUSXMKGF-UHFFFAOYSA-M 0.000 claims 1
- MGZLGERQMWHVOV-UHFFFAOYSA-M 3-(4-fluorophenyl)-1,2-dimethyl-5-phenylpyrazol-1-ium iodide Chemical compound [I-].FC1=CC=C(C=C1)C=1N([N+](=C(C1)C1=CC=CC=C1)C)C MGZLGERQMWHVOV-UHFFFAOYSA-M 0.000 claims 1
- VXMYHJHFRMICKB-UHFFFAOYSA-L 3-(4-tert-butylphenyl)-1,2-dimethyl-5-phenylpyrazol-1-ium sulfate Chemical compound S(=O)(=O)([O-])[O-].C(C)(C)(C)C1=CC=C(C=C1)C=1C=C(N([N+]1C)C)C1=CC=CC=C1.C(C)(C)(C)C1=CC=C(C=C1)C=1C=C(N([N+]1C)C)C1=CC=CC=C1 VXMYHJHFRMICKB-UHFFFAOYSA-L 0.000 claims 1
- RVIFYLGFRPWUKH-UHFFFAOYSA-M Cl(=O)(=O)(=O)[O-].ClC1=C(C=CC(=C1)Cl)C=1N([N+](=C(C1)C1=C(C=C(C=C1)Cl)Cl)C)C Chemical compound Cl(=O)(=O)(=O)[O-].ClC1=C(C=CC(=C1)Cl)C=1N([N+](=C(C1)C1=C(C=C(C=C1)Cl)Cl)C)C RVIFYLGFRPWUKH-UHFFFAOYSA-M 0.000 claims 1
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- WTKZEGDFNFYCGP-UHFFFAOYSA-O Pyrazolium Chemical compound C1=CN[NH+]=C1 WTKZEGDFNFYCGP-UHFFFAOYSA-O 0.000 claims 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US546654A US3930011A (en) | 1975-02-03 | 1975-02-03 | Pyrazolium fungicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS199651B2 true CS199651B2 (en) | 1980-07-31 |
Family
ID=24181410
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS76580A CS199651B2 (en) | 1975-02-03 | 1976-01-29 | Fungicide |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US3930011A (de) |
| JP (1) | JPS51104031A (de) |
| AR (1) | AR217624A1 (de) |
| AT (1) | AT347178B (de) |
| AU (1) | AU500653B2 (de) |
| BE (1) | BE838171R (de) |
| BR (1) | BR7600646A (de) |
| CA (1) | CA1058517A (de) |
| CH (1) | CH594354A5 (de) |
| CS (1) | CS199651B2 (de) |
| DD (1) | DD124703A6 (de) |
| DE (1) | DE2602964A1 (de) |
| DK (1) | DK139833B (de) |
| FI (1) | FI59194C (de) |
| FR (1) | FR2298949A2 (de) |
| GB (1) | GB1534866A (de) |
| IE (1) | IE42949B1 (de) |
| IL (1) | IL48708A (de) |
| IT (1) | IT1053334B (de) |
| NL (1) | NL7600700A (de) |
| NO (1) | NO145039C (de) |
| SE (1) | SE420888B (de) |
| SU (1) | SU644359A3 (de) |
| TR (1) | TR18706A (de) |
| ZA (1) | ZA757951B (de) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4207326A (en) * | 1979-05-21 | 1980-06-10 | Cilag-Chemie A.G. | Antimicrobial quaternary pyrazole derivatives |
| US5470869A (en) * | 1994-01-31 | 1995-11-28 | American Cyanamid Company | Pyrazolium fungicidal compositions |
| GB2294640A (en) * | 1994-11-07 | 1996-05-08 | American Cyanamid Co | Synergistic fungicidal difenzoquat compositions |
| EP4173485A1 (de) * | 2021-10-27 | 2023-05-03 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Proteinaggregation-hemmende verbindungen zur bekämpfung von pflanzenkrankheiten |
-
1975
- 1975-02-03 US US546654A patent/US3930011A/en not_active Expired - Lifetime
- 1975-12-22 ZA ZA00757951A patent/ZA757951B/xx unknown
- 1975-12-23 IL IL48708A patent/IL48708A/xx unknown
- 1975-12-24 AU AU87903/75A patent/AU500653B2/en not_active Expired
- 1975-12-30 GB GB53214/75A patent/GB1534866A/en not_active Expired
-
1976
- 1976-01-09 CA CA243,287A patent/CA1058517A/en not_active Expired
- 1976-01-13 AR AR261918A patent/AR217624A1/es active
- 1976-01-19 IT IT47683/76A patent/IT1053334B/it active
- 1976-01-23 NL NL7600700A patent/NL7600700A/xx not_active Application Discontinuation
- 1976-01-26 DK DK29676AA patent/DK139833B/da not_active IP Right Cessation
- 1976-01-26 FI FI760174A patent/FI59194C/fi not_active IP Right Cessation
- 1976-01-27 DE DE19762602964 patent/DE2602964A1/de not_active Withdrawn
- 1976-01-27 TR TR18706A patent/TR18706A/xx unknown
- 1976-01-29 CS CS76580A patent/CS199651B2/cs unknown
- 1976-02-02 BR BR7600646A patent/BR7600646A/pt unknown
- 1976-02-02 AT AT69776A patent/AT347178B/de not_active IP Right Cessation
- 1976-02-02 BE BE164007A patent/BE838171R/xx not_active IP Right Cessation
- 1976-02-02 SU SU762319208A patent/SU644359A3/ru active
- 1976-02-02 SE SE7601095A patent/SE420888B/xx unknown
- 1976-02-02 NO NO760343A patent/NO145039C/no unknown
- 1976-02-02 CH CH124376A patent/CH594354A5/xx not_active IP Right Cessation
- 1976-02-03 JP JP51010777A patent/JPS51104031A/ja active Pending
- 1976-02-03 DD DD191070A patent/DD124703A6/xx unknown
- 1976-02-03 FR FR7602975A patent/FR2298949A2/fr active Granted
- 1976-02-03 IE IE218/76A patent/IE42949B1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JPS51104031A (de) | 1976-09-14 |
| IL48708A0 (en) | 1976-02-29 |
| NO145039B (no) | 1981-09-21 |
| SU644359A3 (ru) | 1979-01-25 |
| FR2298949B2 (de) | 1979-03-30 |
| FI59194C (fi) | 1981-07-10 |
| FI59194B (fi) | 1981-03-31 |
| IL48708A (en) | 1978-07-31 |
| US3930011A (en) | 1975-12-30 |
| FI760174A (de) | 1976-08-04 |
| IE42949B1 (en) | 1980-11-19 |
| SE7601095L (sv) | 1976-08-03 |
| TR18706A (tr) | 1977-08-10 |
| FR2298949A2 (fr) | 1976-08-27 |
| AR217624A1 (es) | 1980-04-15 |
| CH594354A5 (de) | 1978-01-13 |
| NO145039C (no) | 1982-01-04 |
| DK139833B (da) | 1979-04-30 |
| IT1053334B (it) | 1981-08-31 |
| CA1058517A (en) | 1979-07-17 |
| DK29676A (de) | 1976-08-04 |
| SE420888B (sv) | 1981-11-09 |
| AT347178B (de) | 1978-12-11 |
| DE2602964A1 (de) | 1976-08-05 |
| BR7600646A (pt) | 1976-08-31 |
| IE42949L (en) | 1976-08-03 |
| NL7600700A (nl) | 1976-08-05 |
| DD124703A6 (de) | 1977-03-09 |
| NO760343L (de) | 1976-08-04 |
| ZA757951B (en) | 1976-12-29 |
| BE838171R (fr) | 1976-08-02 |
| AU500653B2 (en) | 1979-05-31 |
| AU8790375A (en) | 1977-06-30 |
| GB1534866A (en) | 1978-12-06 |
| ATA69776A (de) | 1978-04-15 |
| DK139833C (de) | 1979-10-01 |
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