GB955946A - N-polyhaloethylthio compounds and their use as fungicidal compositions - Google Patents
N-polyhaloethylthio compounds and their use as fungicidal compositionsInfo
- Publication number
- GB955946A GB955946A GB143062A GB143062A GB955946A GB 955946 A GB955946 A GB 955946A GB 143062 A GB143062 A GB 143062A GB 143062 A GB143062 A GB 143062A GB 955946 A GB955946 A GB 955946A
- Authority
- GB
- United Kingdom
- Prior art keywords
- tetrachloroethylthio
- sulphonamide
- methyl
- bromine
- chlorine
- 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
- 150000001875 compounds Chemical class 0.000 title abstract 9
- 230000000855 fungicidal effect Effects 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 6
- 125000003368 amide group Chemical group 0.000 abstract 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 6
- 229910052794 bromium Chemical group 0.000 abstract 6
- 239000000460 chlorine Substances 0.000 abstract 6
- 229910052801 chlorine Inorganic materials 0.000 abstract 6
- 229910052757 nitrogen Inorganic materials 0.000 abstract 6
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 6
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 abstract 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 4
- 125000002723 alicyclic group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 abstract 3
- 229940091173 hydantoin Drugs 0.000 abstract 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 abstract 3
- 239000000243 solution Substances 0.000 abstract 3
- -1 1-ethylamyl Chemical group 0.000 abstract 2
- PPAZYICXTAAUHN-UHFFFAOYSA-N 3,4-dibromo-1-(1,1,2,2-tetrachloroethylsulfanyl)pyrrolidine-2,5-dione Chemical compound ClC(C(Cl)Cl)(SN1C(C(C(C1=O)Br)Br)=O)Cl PPAZYICXTAAUHN-UHFFFAOYSA-N 0.000 abstract 2
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 abstract 2
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 abstract 2
- SOWBFZRMHSNYGE-UHFFFAOYSA-N Monoamide-Oxalic acid Natural products NC(=O)C(O)=O SOWBFZRMHSNYGE-UHFFFAOYSA-N 0.000 abstract 2
- DFPAKSUCGFBDDF-ZQBYOMGUSA-N [14c]-nicotinamide Chemical compound N[14C](=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-ZQBYOMGUSA-N 0.000 abstract 2
- YDQUCWMQMWNPLR-UHFFFAOYSA-N [ethyl(sulfamoyl)amino]ethane Chemical compound CCN(CC)S(N)(=O)=O YDQUCWMQMWNPLR-UHFFFAOYSA-N 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- DNSISZSEWVHGLH-UHFFFAOYSA-N butanamide Chemical compound CCCC(N)=O DNSISZSEWVHGLH-UHFFFAOYSA-N 0.000 abstract 2
- OVIZSQRQYWEGON-UHFFFAOYSA-N butane-1-sulfonamide Chemical compound CCCCS(N)(=O)=O OVIZSQRQYWEGON-UHFFFAOYSA-N 0.000 abstract 2
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 2
- 125000000068 chlorophenyl group Chemical group 0.000 abstract 2
- AEOCXXJPGCBFJA-UHFFFAOYSA-N ethionamide Chemical compound CCC1=CC(C(N)=S)=CC=N1 AEOCXXJPGCBFJA-UHFFFAOYSA-N 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 239000000417 fungicide Substances 0.000 abstract 2
- 125000002541 furyl group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 150000001469 hydantoins Chemical class 0.000 abstract 2
- HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical compound CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 abstract 2
- ZFIFHAKCBWOSRN-UHFFFAOYSA-N naphthalene-1-sulfonamide Chemical compound C1=CC=C2C(S(=O)(=O)N)=CC=CC2=C1 ZFIFHAKCBWOSRN-UHFFFAOYSA-N 0.000 abstract 2
- 125000001624 naphthyl group Chemical group 0.000 abstract 2
- COWNFYYYZFRNOY-UHFFFAOYSA-N oxazolidinedione Chemical compound O=C1COC(=O)N1 COWNFYYYZFRNOY-UHFFFAOYSA-N 0.000 abstract 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000004076 pyridyl group Chemical group 0.000 abstract 2
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 abstract 2
- 229940124530 sulfonamide Drugs 0.000 abstract 2
- 150000003456 sulfonamides Chemical class 0.000 abstract 2
- 125000003944 tolyl group Chemical group 0.000 abstract 2
- MGOKAUXOGPGIIT-UHFFFAOYSA-N 1,1,2,2-tetrachloroethanesulfonyl chloride Chemical compound ClC(Cl)C(Cl)(Cl)S(Cl)(=O)=O MGOKAUXOGPGIIT-UHFFFAOYSA-N 0.000 abstract 1
- LCVOCDOSGJHZFH-UHFFFAOYSA-N 1,1,2,2-tetrachloroethyl thiohypochlorite Chemical compound ClSC(Cl)(Cl)C(Cl)Cl LCVOCDOSGJHZFH-UHFFFAOYSA-N 0.000 abstract 1
- RUFAFKWLURMVKG-UHFFFAOYSA-N 1,2,2,2-tetrachloroethyl thiohypochlorite Chemical compound ClSC(Cl)C(Cl)(Cl)Cl RUFAFKWLURMVKG-UHFFFAOYSA-N 0.000 abstract 1
- BEFXMPAXARVEOT-UHFFFAOYSA-N 1-(1,1,2,2-tetrachloroethylsulfanyl)piperidine-2,6-dione Chemical compound ClC(C(Cl)Cl)(SN1C(CCCC1=O)=O)Cl BEFXMPAXARVEOT-UHFFFAOYSA-N 0.000 abstract 1
- DSYDAVMWVFVVRB-UHFFFAOYSA-N 1-(1,1,2,2-tetrachloroethylsulfanyl)pyrrole-2,5-dione Chemical compound ClC(C(Cl)Cl)(SN1C(C=CC1=O)=O)Cl DSYDAVMWVFVVRB-UHFFFAOYSA-N 0.000 abstract 1
- CIDXOAONKMRBSC-UHFFFAOYSA-N 1-(1,1,2,2-tetrachloroethylsulfanyl)pyrrolidine-2,5-dione Chemical compound ClC(C(Cl)Cl)(SN1C(CCC1=O)=O)Cl CIDXOAONKMRBSC-UHFFFAOYSA-N 0.000 abstract 1
- WGTCJLMILBECCY-UHFFFAOYSA-N 4-(1,1,2,2-tetrachloroethylsulfanyl)morpholine-3,5-dione Chemical compound ClC(C(Cl)Cl)(SN1C(COCC1=O)=O)Cl WGTCJLMILBECCY-UHFFFAOYSA-N 0.000 abstract 1
- CCPJJPHDSMAWFC-UHFFFAOYSA-N 4-chloro-N-(1,2-dibromo-1,2-dichloroethyl)sulfanyl-N-methylbenzenesulfonamide Chemical compound BrC(C(Cl)Br)(SN(S(=O)(=O)C1=CC=C(C=C1)Cl)C)Cl CCPJJPHDSMAWFC-UHFFFAOYSA-N 0.000 abstract 1
- NWHYMYHLLZUZDG-UHFFFAOYSA-N 4-chloro-N-methyl-N-(1,1,2,2,2-pentachloroethylsulfanyl)benzenesulfonamide Chemical compound CN(S(=O)(=O)C1=CC=C(C=C1)Cl)SC(C(Cl)(Cl)Cl)(Cl)Cl NWHYMYHLLZUZDG-UHFFFAOYSA-N 0.000 abstract 1
- SUDYATJYRZRXLQ-UHFFFAOYSA-N 4-chloro-N-methyl-N-(1,1,2,2-tetrachloroethylsulfanyl)benzenesulfonamide Chemical compound CN(S(=O)(=O)C1=CC=C(C=C1)Cl)SC(C(Cl)Cl)(Cl)Cl SUDYATJYRZRXLQ-UHFFFAOYSA-N 0.000 abstract 1
- YHGFEJKCEWPBFW-UHFFFAOYSA-N 4-chloro-N-methyl-N-(1,2,2,2-tetrachloroethylsulfanyl)benzenesulfonamide Chemical compound CN(S(=O)(=O)C1=CC=C(C=C1)Cl)SC(C(Cl)(Cl)Cl)Cl YHGFEJKCEWPBFW-UHFFFAOYSA-N 0.000 abstract 1
- SPOKUAMWNZZIGU-UHFFFAOYSA-N 4-chloro-N-methyl-N-(1,2,2-trichloroethenylsulfanyl)benzenesulfonamide Chemical compound CN(S(=O)(=O)C1=CC=C(C=C1)Cl)SC(=C(Cl)Cl)Cl SPOKUAMWNZZIGU-UHFFFAOYSA-N 0.000 abstract 1
- YIROYDNZEPTFOL-UHFFFAOYSA-N 5,5-Dimethylhydantoin Chemical compound CC1(C)NC(=O)NC1=O YIROYDNZEPTFOL-UHFFFAOYSA-N 0.000 abstract 1
- OJRAJPCIEMNDGA-UHFFFAOYSA-N 5,5-dimethyl-3-(1,2,2,2-tetrachloroethylsulfanyl)imidazolidine-2,4-dione Chemical compound ClC(C(Cl)(Cl)Cl)SN1C(NC(C1=O)(C)C)=O OJRAJPCIEMNDGA-UHFFFAOYSA-N 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 1
- XHFYRLJPYIXWGQ-UHFFFAOYSA-N N-(2-bromo-1,2,2-trichloroethyl)sulfanyl-4-chloro-N-methylbenzenesulfonamide Chemical compound BrC(C(SN(S(=O)(=O)C1=CC=C(C=C1)Cl)C)Cl)(Cl)Cl XHFYRLJPYIXWGQ-UHFFFAOYSA-N 0.000 abstract 1
- WINGIJKORPAJSI-UHFFFAOYSA-N N-(4-chlorophenyl)-N-(1,1,2,2-tetrachloroethylsulfanyl)ethanesulfonamide Chemical compound ClC1=CC=C(C=C1)N(S(=O)(=O)CC)SC(C(Cl)Cl)(Cl)Cl WINGIJKORPAJSI-UHFFFAOYSA-N 0.000 abstract 1
- MKSRUUPKMAVDMJ-UHFFFAOYSA-N N-(dimethylsulfamoyl)-N-(1,2,2,2-tetrachloroethylsulfanyl)aniline Chemical compound C1(=CC=CC=C1)N(S(=O)(=O)N(C)C)SC(C(Cl)(Cl)Cl)Cl MKSRUUPKMAVDMJ-UHFFFAOYSA-N 0.000 abstract 1
- VCHHGFBJVNWQCO-UHFFFAOYSA-N N-(dimethylsulfamoyl)-N-(1,2,2-trichloroethenylsulfanyl)aniline Chemical compound C1(=CC=CC=C1)N(S(=O)(=O)N(C)C)SC(=C(Cl)Cl)Cl VCHHGFBJVNWQCO-UHFFFAOYSA-N 0.000 abstract 1
- YDIGBLNJVMPRQL-UHFFFAOYSA-N N-ethyl-N-(1,2,2,2-tetrachloroethylsulfanyl)benzenesulfonamide Chemical compound C(C)N(S(=O)(=O)C1=CC=CC=C1)SC(C(Cl)(Cl)Cl)Cl YDIGBLNJVMPRQL-UHFFFAOYSA-N 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- 239000003995 emulsifying agent Substances 0.000 abstract 1
- 150000003949 imides Chemical class 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- YCVLNLXLOPCQCX-UHFFFAOYSA-N n-(4-chlorophenyl)ethanesulfonamide Chemical compound CCS(=O)(=O)NC1=CC=C(Cl)C=C1 YCVLNLXLOPCQCX-UHFFFAOYSA-N 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000002689 soil Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 229960002317 succinimide Drugs 0.000 abstract 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 231100000167 toxic agent Toxicity 0.000 abstract 1
- 239000003440 toxic substance Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
-
- 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom not containing sulfur-to-oxygen bonds, e.g. polysulfides
-
- 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/46—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with hetero atoms directly attached to the ring nitrogen atom
- C07D207/48—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/92—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
- C07D211/96—Sulfur atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
- C07D233/72—Two oxygen atoms, e.g. hydantoin
- C07D233/80—Two oxygen atoms, e.g. hydantoin with hetero atoms or acyl radicals directly attached to ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/34—Oxygen atoms
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 (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US8394661A | 1961-01-23 | 1961-01-23 | |
| US9547161A | 1961-03-14 | 1961-03-14 | |
| US12184661A | 1961-07-05 | 1961-07-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB955946A true GB955946A (en) | 1964-04-22 |
Family
ID=27374646
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB143062A Expired GB955946A (en) | 1961-01-23 | 1962-01-15 | N-polyhaloethylthio compounds and their use as fungicidal compositions |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE612712A (enrdf_load_stackoverflow) |
| GB (1) | GB955946A (enrdf_load_stackoverflow) |
| NL (3) | NL7011850A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0064657A1 (de) * | 1981-05-07 | 1982-11-17 | Bayer Ag | Ringförmige Sulfenamide, Verfahren zu ihrer Herstellung, sie enthaltende Arzneimittel und deren Herstellung |
-
0
- NL NL273827D patent/NL273827A/xx unknown
- BE BE612712D patent/BE612712A/xx unknown
-
1962
- 1962-01-15 GB GB143062A patent/GB955946A/en not_active Expired
-
1970
- 1970-08-11 NL NL7011850A patent/NL7011850A/xx unknown
- 1970-08-11 NL NL7011851A patent/NL7011851A/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0064657A1 (de) * | 1981-05-07 | 1982-11-17 | Bayer Ag | Ringförmige Sulfenamide, Verfahren zu ihrer Herstellung, sie enthaltende Arzneimittel und deren Herstellung |
Also Published As
| Publication number | Publication date |
|---|---|
| NL7011851A (enrdf_load_stackoverflow) | 1970-12-28 |
| NL273827A (enrdf_load_stackoverflow) | |
| NL7011850A (enrdf_load_stackoverflow) | 1970-12-28 |
| DE1542710A1 (de) | 1970-04-02 |
| BE612712A (enrdf_load_stackoverflow) |
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