DE2430353C2 - 1H-(Pyrido-[3.2-e]-2.1.3-thiadiazin-(4)-on-2.2-dioxide) - Google Patents
1H-(Pyrido-[3.2-e]-2.1.3-thiadiazin-(4)-on-2.2-dioxide)Info
- Publication number
- DE2430353C2 DE2430353C2 DE2430353A DE2430353A DE2430353C2 DE 2430353 C2 DE2430353 C2 DE 2430353C2 DE 2430353 A DE2430353 A DE 2430353A DE 2430353 A DE2430353 A DE 2430353A DE 2430353 C2 DE2430353 C2 DE 2430353C2
- Authority
- DE
- Germany
- Prior art keywords
- dioxide
- parts
- pyrido
- thiadiazin
- weight
- 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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- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- WPUJEWVVTKLMQI-UHFFFAOYSA-N benzene;ethoxyethane Chemical compound CCOCC.C1=CC=CC=C1 WPUJEWVVTKLMQI-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 125000005521 carbonamide group Chemical group 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-O diethylammonium Chemical compound CC[NH2+]CC HPNMFZURTQLUMO-UHFFFAOYSA-O 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- HPYNZHMRTTWQTB-UHFFFAOYSA-N dimethylpyridine Natural products CC1=CC=CN=C1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 1
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-O ethylaminium Chemical compound CC[NH3+] QUSNBJAOOMFDIB-UHFFFAOYSA-O 0.000 description 1
- 241001233957 eudicotyledons Species 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000001605 fetal effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N heptadecan-1-ol Chemical class CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical class CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
- LRDFRRGEGBBSRN-UHFFFAOYSA-N isobutyronitrile Chemical compound CC(C)C#N LRDFRRGEGBBSRN-UHFFFAOYSA-N 0.000 description 1
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N isopropyl alcohol Natural products CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 description 1
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- NZZDEODTCXHCRS-UHFFFAOYSA-N methyl 2-aminopyridine-3-carboxylate Chemical compound COC(=O)C1=CC=CN=C1N NZZDEODTCXHCRS-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 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
- 235000010755 mineral Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- DLMICMXXVVMDNV-UHFFFAOYSA-N n,n-di(propan-2-yl)propan-1-amine Chemical compound CCCN(C(C)C)C(C)C DLMICMXXVVMDNV-UHFFFAOYSA-N 0.000 description 1
- VOVZXURTCKPRDQ-CQSZACIVSA-N n-[4-[chloro(difluoro)methoxy]phenyl]-6-[(3r)-3-hydroxypyrrolidin-1-yl]-5-(1h-pyrazol-5-yl)pyridine-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=NC=C(C(=O)NC=2C=CC(OC(F)(F)Cl)=CC=2)C=C1C1=CC=NN1 VOVZXURTCKPRDQ-CQSZACIVSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000001069 nematicidal effect Effects 0.000 description 1
- 239000005645 nematicide Substances 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
- 150000007530 organic bases Chemical group 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000004476 plant protection product Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 125000005624 silicic acid group Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 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
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Priority Applications (22)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2430353A DE2430353C2 (de) | 1974-06-25 | 1974-06-25 | 1H-(Pyrido-[3.2-e]-2.1.3-thiadiazin-(4)-on-2.2-dioxide) |
JP50055515A JPS5830281B2 (ja) | 1974-06-25 | 1975-05-13 | ジヨソウザイ |
GB22565/75A GB1504919A (en) | 1974-06-25 | 1975-05-23 | Substituted pyridino - 2,1,3 - thiadiazin - (4) - one- 2,2 - dioxides and their use as herbicides |
IL47379A IL47379A (en) | 1974-06-25 | 1975-05-28 | 1h-pyridino (3,2-e)-2,1,3-thiadiazin-(4)-one 2,2-dioxide derivatives their production and herbicidal compositions containing them |
CA228,109A CA1050977A (en) | 1974-06-25 | 1975-05-30 | 1h-(pyridino-(3,2-e)-2,1,3-thiadiazin-(4)-one-2,2-dioxides) |
AU81720/75A AU491423B2 (en) | 1974-06-25 | 1975-05-30 | Ih-(pyridino-[3,2-e] 2,1,3-thiadiazin-(4)-one-2, 2-dioxides |
YU01395/75A YU139575A (en) | 1974-06-25 | 1975-05-30 | Process for the synthesis of substituted 1h-(pyridino-3,2-e)-2,1,3-thiadiazine-(4)-one-2,2-dioxide |
IT49916/75A IT1036913B (it) | 1974-06-25 | 1975-06-04 | Ih(pilidino (3.2. e)2.1.3. tiadia zin 4 one 2.2 biossidi) |
BE157567A BE830505A (fr) | 1974-06-25 | 1975-06-20 | Nouveaux 2,2-dioxydes de pyridino-'(3,2-e)-2,1,3-thiadiazine -(4)-one substitues a activite herbicide |
NL7507406A NL7507406A (nl) | 1974-06-25 | 1975-06-20 | Werkwijze voor de bereiding van gesubstitueerde 2.1.3-thiadiazine-(4)-on-2.2-dioxyden met een herbicide werking. |
PL1975181480A PL96586B1 (pl) | 1974-06-25 | 1975-06-23 | Srodek chwastobojczy |
CH813975A CH610182A5 (en) | 1974-06-25 | 1975-06-23 | Method of controlling undesired vegetation, and herbicidal composition for carrying out the process |
SE7507176A SE423099B (sv) | 1974-06-25 | 1975-06-23 | For anvendning som herbicid avsedd substituerad 1h-(pyridino(3,2-e)-2,1,3-tiadiazin-4-on-2,2-dioxid |
SU752146730A SU655277A3 (ru) | 1974-06-25 | 1975-06-23 | Гербицидное средство |
DD186831A DD118508A5 (en:Method) | 1974-06-25 | 1975-06-23 | |
CS7500004439A CS185693B2 (en) | 1974-06-25 | 1975-06-23 | Herbicidal agent |
BR5076/75D BR7503946A (pt) | 1974-06-25 | 1975-06-24 | 1h-(piridino-(3.2-e)-2.1.3-tiadiazin-(4)-on-2.2-dioxidos) |
ZA00754013A ZA754013B (en) | 1974-06-25 | 1975-06-24 | 1h-<pyridino-(3,2-e)-2,1,3-thiadiazin-(4)-one-2,2-dioxides> |
ES438848A ES438848A1 (es) | 1974-06-25 | 1975-06-24 | Procedimiento para la obtencion de 2,2-dioxidos de 1h-(pi- ridino-(3, 2-e)-2, 1, 3-tiadiazin-(4)-ona). |
HU75BA00003289A HU172325B (hu) | 1974-06-25 | 1975-06-24 | Gerbicidy soderzhahhie zamehhennye piridino-skobka-2,3-e-skobka zakryta-2,1,3-tiadiazin-4-on-2,4,-dioksidy, i sposob poluchenija aktivnykh agentov |
AT482975A AT342916B (de) | 1974-06-25 | 1975-06-24 | Herbizid |
FR7519894A FR2276309A1 (fr) | 1974-06-25 | 1975-06-25 | 2,2-dioxydes de 1h-(pyridino-(3,2-e)-2,1,3-thiadiazine-(4)-one utilisables comme herbicides |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2430353A DE2430353C2 (de) | 1974-06-25 | 1974-06-25 | 1H-(Pyrido-[3.2-e]-2.1.3-thiadiazin-(4)-on-2.2-dioxide) |
Publications (2)
Publication Number | Publication Date |
---|---|
DE2430353A1 DE2430353A1 (de) | 1976-01-15 |
DE2430353C2 true DE2430353C2 (de) | 1984-02-09 |
Family
ID=5918861
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE2430353A Expired DE2430353C2 (de) | 1974-06-25 | 1974-06-25 | 1H-(Pyrido-[3.2-e]-2.1.3-thiadiazin-(4)-on-2.2-dioxide) |
Country Status (21)
Country | Link |
---|---|
JP (1) | JPS5830281B2 (en:Method) |
AT (1) | AT342916B (en:Method) |
BE (1) | BE830505A (en:Method) |
BR (1) | BR7503946A (en:Method) |
CA (1) | CA1050977A (en:Method) |
CH (1) | CH610182A5 (en:Method) |
CS (1) | CS185693B2 (en:Method) |
DD (1) | DD118508A5 (en:Method) |
DE (1) | DE2430353C2 (en:Method) |
ES (1) | ES438848A1 (en:Method) |
FR (1) | FR2276309A1 (en:Method) |
GB (1) | GB1504919A (en:Method) |
HU (1) | HU172325B (en:Method) |
IL (1) | IL47379A (en:Method) |
IT (1) | IT1036913B (en:Method) |
NL (1) | NL7507406A (en:Method) |
PL (1) | PL96586B1 (en:Method) |
SE (1) | SE423099B (en:Method) |
SU (1) | SU655277A3 (en:Method) |
YU (1) | YU139575A (en:Method) |
ZA (1) | ZA754013B (en:Method) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3103066A1 (de) | 1981-01-30 | 1982-08-26 | Basf Ag, 6700 Ludwigshafen | "verfahren zur herstellung von butadiendinitrilen" |
-
1974
- 1974-06-25 DE DE2430353A patent/DE2430353C2/de not_active Expired
-
1975
- 1975-05-13 JP JP50055515A patent/JPS5830281B2/ja not_active Expired
- 1975-05-23 GB GB22565/75A patent/GB1504919A/en not_active Expired
- 1975-05-28 IL IL47379A patent/IL47379A/xx unknown
- 1975-05-30 CA CA228,109A patent/CA1050977A/en not_active Expired
- 1975-05-30 YU YU01395/75A patent/YU139575A/xx unknown
- 1975-06-04 IT IT49916/75A patent/IT1036913B/it active
- 1975-06-20 BE BE157567A patent/BE830505A/xx not_active IP Right Cessation
- 1975-06-20 NL NL7507406A patent/NL7507406A/xx not_active Application Discontinuation
- 1975-06-23 SU SU752146730A patent/SU655277A3/ru active
- 1975-06-23 PL PL1975181480A patent/PL96586B1/pl unknown
- 1975-06-23 CH CH813975A patent/CH610182A5/xx not_active IP Right Cessation
- 1975-06-23 DD DD186831A patent/DD118508A5/xx unknown
- 1975-06-23 SE SE7507176A patent/SE423099B/xx not_active IP Right Cessation
- 1975-06-23 CS CS7500004439A patent/CS185693B2/cs unknown
- 1975-06-24 AT AT482975A patent/AT342916B/de not_active IP Right Cessation
- 1975-06-24 ZA ZA00754013A patent/ZA754013B/xx unknown
- 1975-06-24 BR BR5076/75D patent/BR7503946A/pt unknown
- 1975-06-24 HU HU75BA00003289A patent/HU172325B/hu not_active IP Right Cessation
- 1975-06-24 ES ES438848A patent/ES438848A1/es not_active Expired
- 1975-06-25 FR FR7519894A patent/FR2276309A1/fr active Granted
Also Published As
Publication number | Publication date |
---|---|
IL47379A (en) | 1978-01-31 |
BE830505A (fr) | 1975-12-22 |
HU172325B (hu) | 1978-08-28 |
PL96586B1 (pl) | 1978-01-31 |
SE7507176L (sv) | 1975-12-29 |
SU655277A3 (ru) | 1979-03-30 |
FR2276309A1 (fr) | 1976-01-23 |
CS185693B2 (en) | 1978-10-31 |
ZA754013B (en) | 1976-06-30 |
ES438848A1 (es) | 1977-01-16 |
SE423099B (sv) | 1982-04-13 |
AT342916B (de) | 1978-04-25 |
YU139575A (en) | 1982-02-28 |
JPS511642A (en:Method) | 1976-01-08 |
GB1504919A (en) | 1978-03-22 |
CA1050977A (en) | 1979-03-20 |
IT1036913B (it) | 1979-10-30 |
AU8172075A (en) | 1976-12-02 |
JPS5830281B2 (ja) | 1983-06-28 |
NL7507406A (nl) | 1975-12-30 |
FR2276309B1 (en:Method) | 1978-09-08 |
CH610182A5 (en) | 1979-04-12 |
DE2430353A1 (de) | 1976-01-15 |
DD118508A5 (en:Method) | 1976-03-12 |
IL47379A0 (en) | 1975-07-28 |
BR7503946A (pt) | 1976-07-06 |
ATA482975A (de) | 1977-08-15 |
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