IE43527B1 - Nitroaryloxyalkanecarboxylic acid derivatives and their use as herbicides - Google Patents
Nitroaryloxyalkanecarboxylic acid derivatives and their use as herbicidesInfo
- Publication number
- IE43527B1 IE43527B1 IE1857/76A IE185776A IE43527B1 IE 43527 B1 IE43527 B1 IE 43527B1 IE 1857/76 A IE1857/76 A IE 1857/76A IE 185776 A IE185776 A IE 185776A IE 43527 B1 IE43527 B1 IE 43527B1
- Authority
- IE
- Ireland
- Prior art keywords
- carbon atoms
- acid
- compound
- process according
- reaction
- Prior art date
Links
- 239000002253 acid Substances 0.000 title abstract description 52
- 239000004009 herbicide Substances 0.000 title abstract description 6
- 150000001875 compounds Chemical class 0.000 abstract description 67
- 150000003839 salts Chemical class 0.000 abstract description 32
- 239000003085 diluting agent Substances 0.000 abstract description 19
- 239000000203 mixture Substances 0.000 abstract description 17
- 150000007513 acids Chemical class 0.000 abstract description 16
- 125000000217 alkyl group Chemical group 0.000 abstract description 15
- 150000002148 esters Chemical class 0.000 abstract description 14
- 125000003118 aryl group Chemical group 0.000 abstract description 9
- 229910052801 chlorine Inorganic materials 0.000 abstract description 9
- 239000007788 liquid Substances 0.000 abstract description 8
- 229910052751 metal Inorganic materials 0.000 abstract description 8
- 239000002184 metal Substances 0.000 abstract description 8
- 150000001768 cations Chemical class 0.000 abstract description 7
- 239000003795 chemical substances by application Substances 0.000 abstract description 7
- 239000003995 emulsifying agent Substances 0.000 abstract description 6
- 230000002363 herbicidal effect Effects 0.000 abstract description 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract description 5
- 239000002270 dispersing agent Substances 0.000 abstract description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract description 4
- 239000007787 solid Substances 0.000 abstract description 4
- 239000004094 surface-active agent Substances 0.000 abstract description 4
- 239000004480 active ingredient Substances 0.000 abstract description 3
- 125000003710 aryl alkyl group Chemical group 0.000 abstract description 3
- 125000000129 anionic group Chemical group 0.000 abstract description 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract description 2
- 229920005610 lignin Polymers 0.000 abstract description 2
- 229920000609 methyl cellulose Polymers 0.000 abstract description 2
- 239000001923 methylcellulose Substances 0.000 abstract description 2
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- 239000002699 waste material Substances 0.000 abstract description 2
- 235000013877 carbamide Nutrition 0.000 abstract 1
- 150000005181 nitrobenzenes Chemical class 0.000 abstract 1
- 150000003918 triazines Chemical class 0.000 abstract 1
- 150000003672 ureas Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 description 53
- 125000004432 carbon atom Chemical group C* 0.000 description 44
- -1 alkyl radical Chemical class 0.000 description 31
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- 238000006243 chemical reaction Methods 0.000 description 27
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- 239000007795 chemical reaction product Substances 0.000 description 6
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- 239000000706 filtrate Substances 0.000 description 6
- 238000009472 formulation Methods 0.000 description 6
- 229910052736 halogen Inorganic materials 0.000 description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 6
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- 150000001412 amines Chemical class 0.000 description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
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- 239000000194 fatty acid Substances 0.000 description 1
- RAQDACVRFCEPDA-UHFFFAOYSA-L ferrous carbonate Chemical compound [Fe+2].[O-]C([O-])=O RAQDACVRFCEPDA-UHFFFAOYSA-L 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229910003439 heavy metal oxide Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229960004705 kojic acid Drugs 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 229940112735 lead carbonate Drugs 0.000 description 1
- ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- JILPJDVXYVTZDQ-UHFFFAOYSA-N lithium methoxide Chemical compound [Li+].[O-]C JILPJDVXYVTZDQ-UHFFFAOYSA-N 0.000 description 1
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 1
- 229910001947 lithium oxide Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- QWDJLDTYWNBUKE-UHFFFAOYSA-L magnesium bicarbonate Chemical compound [Mg+2].OC([O-])=O.OC([O-])=O QWDJLDTYWNBUKE-UHFFFAOYSA-L 0.000 description 1
- 239000002370 magnesium bicarbonate Substances 0.000 description 1
- 229910000022 magnesium bicarbonate Inorganic materials 0.000 description 1
- 235000014824 magnesium bicarbonate Nutrition 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011656 manganese carbonate Substances 0.000 description 1
- 229940093474 manganese carbonate Drugs 0.000 description 1
- 235000006748 manganese carbonate Nutrition 0.000 description 1
- 229910000016 manganese(II) carbonate Inorganic materials 0.000 description 1
- XMWCXZJXESXBBY-UHFFFAOYSA-L manganese(ii) carbonate Chemical compound [Mn+2].[O-]C([O-])=O XMWCXZJXESXBBY-UHFFFAOYSA-L 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- VBWFYEFYHJRJER-UHFFFAOYSA-N methyl 4-(hydroxymethyl)benzoate Chemical compound COC(=O)C1=CC=C(CO)C=C1 VBWFYEFYHJRJER-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 235000019713 millet Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- MNZMMCVIXORAQL-UHFFFAOYSA-N naphthalene-2,6-diol Chemical compound C1=C(O)C=CC2=CC(O)=CC=C21 MNZMMCVIXORAQL-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910000008 nickel(II) carbonate Inorganic materials 0.000 description 1
- ZULUUIKRFGGGTL-UHFFFAOYSA-L nickel(ii) carbonate Chemical compound [Ni+2].[O-]C([O-])=O ZULUUIKRFGGGTL-UHFFFAOYSA-L 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- KLAKIAVEMQMVBT-UHFFFAOYSA-N p-hydroxy-phenacyl alcohol Natural products OCC(=O)C1=CC=C(O)C=C1 KLAKIAVEMQMVBT-UHFFFAOYSA-N 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- BOKVSRHWZPCJRN-UHFFFAOYSA-N propan-2-yl 2-chloropropanoate Chemical compound CC(C)OC(=O)C(C)Cl BOKVSRHWZPCJRN-UHFFFAOYSA-N 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 235000009736 ragweed Nutrition 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004291 sulphur dioxide Substances 0.000 description 1
- 235000010269 sulphur dioxide Nutrition 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- ZPHGMBGIFODUMF-UHFFFAOYSA-N thiophen-2-ylmethanol Chemical compound OCC1=CC=CS1 ZPHGMBGIFODUMF-UHFFFAOYSA-N 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- CVNKFOIOZXAFBO-UHFFFAOYSA-J tin(4+);tetrahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[Sn+4] CVNKFOIOZXAFBO-UHFFFAOYSA-J 0.000 description 1
- WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/27—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
- C07C205/35—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C205/36—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system
- C07C205/37—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/39—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by esterified hydroxy groups
- C07C205/42—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by esterified hydroxy groups having nitro groups or esterified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C205/43—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by esterified hydroxy groups having nitro groups or esterified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyrrole Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19752537201 DE2537201A1 (de) | 1975-08-21 | 1975-08-21 | Nitroaryloxy-alkan-carbonsaeure- derivate, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE43527L IE43527L (en) | 1977-02-21 |
| IE43527B1 true IE43527B1 (en) | 1981-03-25 |
Family
ID=5954482
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE1857/76A IE43527B1 (en) | 1975-08-21 | 1976-08-20 | Nitroaryloxyalkanecarboxylic acid derivatives and their use as herbicides |
Country Status (23)
| Country | Link |
|---|---|
| JP (1) | JPS5321128A (forum.php) |
| AR (1) | AR216905A1 (forum.php) |
| AT (1) | AT348823B (forum.php) |
| AU (1) | AU504239B2 (forum.php) |
| BE (1) | BE845382A (forum.php) |
| BR (1) | BR7605397A (forum.php) |
| CA (1) | CA1079746A (forum.php) |
| CS (1) | CS189023B2 (forum.php) |
| DD (1) | DD127556A5 (forum.php) |
| DE (1) | DE2537201A1 (forum.php) |
| DK (1) | DK376676A (forum.php) |
| ES (1) | ES450853A1 (forum.php) |
| FR (1) | FR2321478A1 (forum.php) |
| GB (1) | GB1501528A (forum.php) |
| IE (1) | IE43527B1 (forum.php) |
| IL (1) | IL50297A0 (forum.php) |
| LU (1) | LU75633A1 (forum.php) |
| NL (1) | NL7609308A (forum.php) |
| PL (1) | PL105489B1 (forum.php) |
| SE (1) | SE7609228L (forum.php) |
| SU (1) | SU604458A3 (forum.php) |
| TR (1) | TR19460A (forum.php) |
| ZA (1) | ZA765006B (forum.php) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5310682A (en) * | 1992-06-17 | 1994-05-10 | Indiana University Foundation | Fluorogenic reagents for detection of glycoconjugates, α-ketoacids and diketones |
| MX2009008934A (es) * | 2007-02-26 | 2009-08-28 | Dow Agrosciences Llc | Proceso para la preparacion de algunas sulfiliminas sustituidas. |
-
1975
- 1975-08-21 DE DE19752537201 patent/DE2537201A1/de active Pending
-
1976
- 1976-08-18 BR BR7605397A patent/BR7605397A/pt unknown
- 1976-08-18 IL IL50297A patent/IL50297A0/xx unknown
- 1976-08-19 SU SU762387321A patent/SU604458A3/ru active
- 1976-08-19 TR TR19460A patent/TR19460A/xx unknown
- 1976-08-19 DD DD194399A patent/DD127556A5/xx unknown
- 1976-08-19 SE SE7609228A patent/SE7609228L/xx unknown
- 1976-08-19 PL PL1976191899A patent/PL105489B1/pl unknown
- 1976-08-19 CS CS765400A patent/CS189023B2/cs unknown
- 1976-08-19 GB GB34608/76A patent/GB1501528A/en not_active Expired
- 1976-08-20 CA CA259,538A patent/CA1079746A/en not_active Expired
- 1976-08-20 DK DK376676A patent/DK376676A/da unknown
- 1976-08-20 FR FR7625277A patent/FR2321478A1/fr not_active Withdrawn
- 1976-08-20 NL NL7609308A patent/NL7609308A/xx not_active Application Discontinuation
- 1976-08-20 ZA ZA765006A patent/ZA765006B/xx unknown
- 1976-08-20 AT AT619476A patent/AT348823B/de not_active IP Right Cessation
- 1976-08-20 AR AR264400A patent/AR216905A1/es active
- 1976-08-20 BE BE169963A patent/BE845382A/xx unknown
- 1976-08-20 ES ES450853A patent/ES450853A1/es not_active Expired
- 1976-08-20 LU LU75633A patent/LU75633A1/xx unknown
- 1976-08-20 IE IE1857/76A patent/IE43527B1/en unknown
- 1976-08-21 JP JP9923576A patent/JPS5321128A/ja active Pending
- 1976-08-23 AU AU17046/76A patent/AU504239B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| AU1704676A (en) | 1978-03-02 |
| DK376676A (da) | 1977-02-22 |
| ES450853A1 (es) | 1977-12-01 |
| FR2321478A1 (fr) | 1977-03-18 |
| BE845382A (fr) | 1977-02-21 |
| IE43527L (en) | 1977-02-21 |
| CA1079746A (en) | 1980-06-17 |
| BR7605397A (pt) | 1977-08-16 |
| LU75633A1 (forum.php) | 1977-04-22 |
| AR216905A1 (es) | 1980-02-15 |
| CS189023B2 (en) | 1979-03-30 |
| ZA765006B (en) | 1977-07-27 |
| SU604458A3 (ru) | 1978-04-25 |
| SE7609228L (sv) | 1977-02-22 |
| AT348823B (de) | 1979-03-12 |
| PL105489B1 (pl) | 1979-10-31 |
| JPS5321128A (en) | 1978-02-27 |
| ATA619476A (de) | 1978-07-15 |
| AU504239B2 (en) | 1979-10-04 |
| TR19460A (tr) | 1979-05-01 |
| GB1501528A (en) | 1978-02-15 |
| IL50297A0 (en) | 1976-10-31 |
| DE2537201A1 (de) | 1977-03-03 |
| NL7609308A (nl) | 1977-02-23 |
| DD127556A5 (forum.php) | 1977-09-28 |
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