NO119248B - - Google Patents
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- Publication number
- NO119248B NO119248B NO231068A NO231068A NO119248B NO 119248 B NO119248 B NO 119248B NO 231068 A NO231068 A NO 231068A NO 231068 A NO231068 A NO 231068A NO 119248 B NO119248 B NO 119248B
- Authority
- NO
- Norway
- Prior art keywords
- carbamylethyl
- carbamylalkyl
- ethyl
- carbon atoms
- halogenated
- Prior art date
Links
- -1 N-(2-carbamylethyl)-4-n-butoxybenzylamine Chemical compound 0.000 claims description 70
- 238000000034 method Methods 0.000 claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- FBCCMZVIWNDFMO-UHFFFAOYSA-N dichloroacetyl chloride Chemical compound ClC(Cl)C(Cl)=O FBCCMZVIWNDFMO-UHFFFAOYSA-N 0.000 claims description 8
- 150000004820 halides Chemical class 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- PVFOMCVHYWHZJE-UHFFFAOYSA-N trichloroacetyl chloride Chemical compound ClC(=O)C(Cl)(Cl)Cl PVFOMCVHYWHZJE-UHFFFAOYSA-N 0.000 claims description 3
- YMVFJGSXZNNUDW-UHFFFAOYSA-N (4-chlorophenyl)methanamine Chemical compound NCC1=CC=C(Cl)C=C1 YMVFJGSXZNNUDW-UHFFFAOYSA-N 0.000 claims description 2
- QVYUMWXPBVFSFT-UHFFFAOYSA-N 3-[(4-chlorophenyl)methylamino]propanamide Chemical compound NC(=O)CCNCC1=CC=C(Cl)C=C1 QVYUMWXPBVFSFT-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 235000010290 biphenyl Nutrition 0.000 claims description 2
- 239000004305 biphenyl Substances 0.000 claims description 2
- 125000002541 furyl group Chemical group 0.000 claims description 2
- 125000001624 naphthyl group Chemical group 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- 125000001589 carboacyl group Chemical group 0.000 claims 1
- 239000000470 constituent Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 description 23
- 239000000460 chlorine Substances 0.000 description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 14
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 13
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 238000004458 analytical method Methods 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 10
- WCGGWVOVFQNRRS-UHFFFAOYSA-N dichloroacetamide Chemical compound NC(=O)C(Cl)Cl WCGGWVOVFQNRRS-UHFFFAOYSA-N 0.000 description 10
- 238000003756 stirring Methods 0.000 description 9
- UPQQXPKAYZYUKO-UHFFFAOYSA-N 2,2,2-trichloroacetamide Chemical compound OC(=N)C(Cl)(Cl)Cl UPQQXPKAYZYUKO-UHFFFAOYSA-N 0.000 description 8
- 239000000543 intermediate Substances 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 150000003974 aralkylamines Chemical class 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- QDFVOZRHRGLKFZ-UHFFFAOYSA-N 3-[(2,4-dichlorophenyl)methylamino]propanamide Chemical compound NC(=O)CCNCC1=CC=C(Cl)C=C1Cl QDFVOZRHRGLKFZ-UHFFFAOYSA-N 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- FZOZVLOYQISHSC-UHFFFAOYSA-N methyl 3-[(4-propan-2-ylphenyl)methylamino]propanoate Chemical compound COC(=O)CCNCC1=CC=C(C(C)C)C=C1 FZOZVLOYQISHSC-UHFFFAOYSA-N 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- ORCCSQMJUGMAQU-UHFFFAOYSA-N 2,2,2-tribromoacetamide Chemical compound NC(=O)C(Br)(Br)Br ORCCSQMJUGMAQU-UHFFFAOYSA-N 0.000 description 2
- KFVJKKAUSPPANZ-UHFFFAOYSA-N 3-[(2,2-dichloroacetyl)-[(2,4-dichlorophenyl)methyl]amino]propanamide Chemical compound NC(=O)CCN(CC1=C(Cl)C=C(Cl)C=C1)C(=O)C(Cl)Cl KFVJKKAUSPPANZ-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 description 2
- 241000699800 Cricetinae Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000003973 alkyl amines Chemical class 0.000 description 2
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000037396 body weight Effects 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 125000001475 halogen functional group Chemical group 0.000 description 2
- 150000002431 hydrogen Chemical group 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 239000013067 intermediate product Substances 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- RQHMQURGSQBBJY-UHFFFAOYSA-N (2,2-dichloroacetyl) 2,2-dichloroacetate Chemical compound ClC(Cl)C(=O)OC(=O)C(Cl)Cl RQHMQURGSQBBJY-UHFFFAOYSA-N 0.000 description 1
- SJUKJZSTBBSGHF-UHFFFAOYSA-N (2,4-dichlorophenyl)methanamine Chemical compound NCC1=CC=C(Cl)C=C1Cl SJUKJZSTBBSGHF-UHFFFAOYSA-N 0.000 description 1
- YQSHYGCCYVPRDI-UHFFFAOYSA-N (4-propan-2-ylphenyl)methanamine Chemical compound CC(C)C1=CC=C(CN)C=C1 YQSHYGCCYVPRDI-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- YUIKPESWSMJSMP-UHFFFAOYSA-N 2,2-dibromoacetamide Chemical compound NC(=O)C(Br)Br YUIKPESWSMJSMP-UHFFFAOYSA-N 0.000 description 1
- IPKCHUGFUGHNRZ-UHFFFAOYSA-N 2,2-dichloropropanoyl chloride Chemical compound CC(Cl)(Cl)C(Cl)=O IPKCHUGFUGHNRZ-UHFFFAOYSA-N 0.000 description 1
- IOXOZOPLBFXYLM-UHFFFAOYSA-N 2-(4-nitrophenyl)ethanamine Chemical compound NCCC1=CC=C([N+]([O-])=O)C=C1 IOXOZOPLBFXYLM-UHFFFAOYSA-N 0.000 description 1
- FUFKQVOYFRHNKD-UHFFFAOYSA-N 2-[[2-(4-nitrophenyl)ethylamino]methyl]butanamide Chemical compound C(N)(=O)C(CNCCC1=CC=C(C=C1)[N+](=O)[O-])CC FUFKQVOYFRHNKD-UHFFFAOYSA-N 0.000 description 1
- GKRKWDWETUTQOT-UHFFFAOYSA-N 2-bromo-2-chloroacetamide Chemical compound NC(=O)C(Cl)Br GKRKWDWETUTQOT-UHFFFAOYSA-N 0.000 description 1
- AKSLRYGHJVUELA-UHFFFAOYSA-N 2-bromobutanamide Chemical compound CCC(Br)C(N)=O AKSLRYGHJVUELA-UHFFFAOYSA-N 0.000 description 1
- LPNSCOVIJFIXTJ-UHFFFAOYSA-N 2-methylidenebutanamide Chemical compound CCC(=C)C(N)=O LPNSCOVIJFIXTJ-UHFFFAOYSA-N 0.000 description 1
- WGTASENVNYJZBK-UHFFFAOYSA-N 3,4,5-trimethoxyamphetamine Chemical compound COC1=CC(CC(C)N)=CC(OC)=C1OC WGTASENVNYJZBK-UHFFFAOYSA-N 0.000 description 1
- GGJZFUWYCGSBCO-UHFFFAOYSA-N 3-(benzylamino)propanamide Chemical compound NC(=O)CCNCC1=CC=CC=C1 GGJZFUWYCGSBCO-UHFFFAOYSA-N 0.000 description 1
- LEEWFQPRAUBGBN-UHFFFAOYSA-N 3-(thiophen-2-ylmethylamino)propanamide Chemical compound NC(=O)CCNCC1=CC=CS1 LEEWFQPRAUBGBN-UHFFFAOYSA-N 0.000 description 1
- YPVUSIPJALAKDL-UHFFFAOYSA-N 3-[(4-chlorophenyl)methyl-(2,2,2-trichloroacetyl)amino]propanamide Chemical compound NC(=O)CCN(CC1=CC=C(Cl)C=C1)C(=O)C(Cl)(Cl)Cl YPVUSIPJALAKDL-UHFFFAOYSA-N 0.000 description 1
- PLCQPORWRCTOAJ-UHFFFAOYSA-N 3-[(4-nitrophenyl)methylamino]propanamide Chemical compound NC(=O)CCNCC1=CC=C([N+]([O-])=O)C=C1 PLCQPORWRCTOAJ-UHFFFAOYSA-N 0.000 description 1
- RRNUDDMPQIAHLB-UHFFFAOYSA-N 3-[(5-chloropyridin-2-yl)methylamino]-2-methylpropanamide Chemical compound C(N)(=O)C(CNCC1=NC=C(C=C1)Cl)C RRNUDDMPQIAHLB-UHFFFAOYSA-N 0.000 description 1
- UDRMZPXGLPXUCE-UHFFFAOYSA-N 3-[2-phenylethyl-(2,2,2-trichloroacetyl)amino]propanamide Chemical compound C1(=CC=CC=C1)CCN(C(C(Cl)(Cl)Cl)=O)CCC(N)=O UDRMZPXGLPXUCE-UHFFFAOYSA-N 0.000 description 1
- AETQPFGDQMISHC-UHFFFAOYSA-N 3-[benzyl-(2,2,2-trichloroacetyl)amino]propanamide Chemical compound NC(=O)CCN(CC1=CC=CC=C1)C(=O)C(Cl)(Cl)Cl AETQPFGDQMISHC-UHFFFAOYSA-N 0.000 description 1
- AMKPQMFZCBTTAT-UHFFFAOYSA-N 3-ethylaniline Chemical compound CCC1=CC=CC(N)=C1 AMKPQMFZCBTTAT-UHFFFAOYSA-N 0.000 description 1
- 241000224489 Amoeba Species 0.000 description 1
- RCHJMHPHQDHZTO-UHFFFAOYSA-N C(N)(=O)C(CNCC1=CC(=C(C(=C1)Br)Br)Br)C Chemical compound C(N)(=O)C(CNCC1=CC(=C(C(=C1)Br)Br)Br)C RCHJMHPHQDHZTO-UHFFFAOYSA-N 0.000 description 1
- 101100037762 Caenorhabditis elegans rnh-2 gene Proteins 0.000 description 1
- NWGZUWCSFIOZOL-UHFFFAOYSA-N Cl.C(N)(=O)CCNCC1=CC=C(C=C1)C(C)C Chemical compound Cl.C(N)(=O)CCNCC1=CC=C(C=C1)C(C)C NWGZUWCSFIOZOL-UHFFFAOYSA-N 0.000 description 1
- 102000006835 Lamins Human genes 0.000 description 1
- 108010047294 Lamins Proteins 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- XTUVJUMINZSXGF-UHFFFAOYSA-N N-methylcyclohexylamine Chemical compound CNC1CCCCC1 XTUVJUMINZSXGF-UHFFFAOYSA-N 0.000 description 1
- ZDGWGNDTQZGISB-UHFFFAOYSA-N acetic acid;perchloric acid Chemical compound CC(O)=O.OCl(=O)(=O)=O ZDGWGNDTQZGISB-UHFFFAOYSA-N 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
- 230000003569 amebicidal effect Effects 0.000 description 1
- CMWYOMQKNDVFMD-UHFFFAOYSA-N benzene;pentane Chemical compound CCCCC.C1=CC=CC=C1 CMWYOMQKNDVFMD-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 230000000973 chemotherapeutic effect Effects 0.000 description 1
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
- NISGSNTVMOOSJQ-UHFFFAOYSA-N cyclopentanamine Chemical compound NC1CCCC1 NISGSNTVMOOSJQ-UHFFFAOYSA-N 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- PGLTVOMIXTUURA-UHFFFAOYSA-N iodoacetamide Chemical compound NC(=O)CI PGLTVOMIXTUURA-UHFFFAOYSA-N 0.000 description 1
- 210000005053 lamin Anatomy 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- GFEBJXSHSRTVII-UHFFFAOYSA-N methyl 3-[(4-butoxyphenyl)methylamino]-2-methylpropanoate Chemical compound C(=O)(OC)C(CNCC1=CC=C(C=C1)OCCCC)C GFEBJXSHSRTVII-UHFFFAOYSA-N 0.000 description 1
- JMFMZDGVNSNHMC-UHFFFAOYSA-N methyl 3-[(4-hexylphenyl)methylamino]propanoate Chemical compound C(=O)(OC)CCNCC1=CC=C(C=C1)CCCCCC JMFMZDGVNSNHMC-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 125000003884 phenylalkyl group Chemical group 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24C—DOMESTIC STOVES OR RANGES ; DETAILS OF DOMESTIC STOVES OR RANGES, OF GENERAL APPLICATION
- F24C15/00—Details
- F24C15/22—Reflectors for radiation heaters
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24C—DOMESTIC STOVES OR RANGES ; DETAILS OF DOMESTIC STOVES OR RANGES, OF GENERAL APPLICATION
- F24C5/00—Stoves or ranges for liquid fuels
- F24C5/02—Stoves or ranges for liquid fuels with evaporation burners, e.g. dish type
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Air-Conditioning For Vehicles (AREA)
- Gas Burners (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Optical Elements Other Than Lenses (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE6041390 | 1967-06-15 | ||
| BE6041783 | 1968-06-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO119248B true NO119248B (de) | 1970-04-20 |
Family
ID=25662071
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO231068A NO119248B (de) | 1967-06-15 | 1968-06-13 |
Country Status (5)
| Country | Link |
|---|---|
| AT (1) | AT285111B (de) |
| CH (1) | CH518495A (de) |
| DK (1) | DK122910B (de) |
| ES (1) | ES355430A1 (de) |
| NO (1) | NO119248B (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ITBL20120012A1 (it) * | 2012-12-28 | 2014-06-29 | Zardini Kachelofen S N C Di Sabrin A Zardini & C | Stufa con alimentazione a biocarburante in camera di combustione chiusa |
-
1968
- 1968-06-11 CH CH869568A patent/CH518495A/fr not_active IP Right Cessation
- 1968-06-13 NO NO231068A patent/NO119248B/no unknown
- 1968-06-14 ES ES355430A patent/ES355430A1/es not_active Expired
- 1968-06-14 DK DK279868A patent/DK122910B/da unknown
- 1968-06-17 AT AT578668A patent/AT285111B/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DK122910B (da) | 1972-04-24 |
| AT285111B (de) | 1970-10-12 |
| CH518495A (fr) | 1972-01-31 |
| ES355430A1 (es) | 1970-03-01 |
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