BE565945A - - Google Patents
Info
- Publication number
- BE565945A BE565945A BE565945DA BE565945A BE 565945 A BE565945 A BE 565945A BE 565945D A BE565945D A BE 565945DA BE 565945 A BE565945 A BE 565945A
- Authority
- BE
- Belgium
- Prior art keywords
- emi
- active material
- compounds described
- cryptogams
- chlorine
- Prior art date
Links
- 239000000203 mixture Substances 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 7
- 239000011149 active material Substances 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- 239000008247 solid mixture Substances 0.000 claims description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 1
- 125000003963 dichloro group Chemical group Cl* 0.000 claims 1
- 230000035943 smell Effects 0.000 claims 1
- 230000000855 fungicidal effect Effects 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 239000000417 fungicide Substances 0.000 description 4
- 230000001274 anti-cryptogamic effect Effects 0.000 description 3
- -1 for example Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- QIMMUPPBPVKWKM-UHFFFAOYSA-N 2-methylnaphthalene Chemical compound C1=CC=CC2=CC(C)=CC=C21 QIMMUPPBPVKWKM-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- SKKUAUZTZZRYPW-UHFFFAOYSA-N 1-chloro-2,4-dinitronaphthalene Chemical compound C1=CC=CC2=C(Cl)C([N+](=O)[O-])=CC([N+]([O-])=O)=C21 SKKUAUZTZZRYPW-UHFFFAOYSA-N 0.000 description 1
- GKQHIYSTBXDYNQ-UHFFFAOYSA-M 1-dodecylpyridin-1-ium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+]1=CC=CC=C1 GKQHIYSTBXDYNQ-UHFFFAOYSA-M 0.000 description 1
- UAZLASMTBCLJKO-UHFFFAOYSA-N 2-decylbenzenesulfonic acid Chemical compound CCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O UAZLASMTBCLJKO-UHFFFAOYSA-N 0.000 description 1
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 1
- IXBUVPSMFSZIRK-UHFFFAOYSA-J C(N)([S-])=S.[Zn+2].[Zn+2].C=C.C(N)([S-])=S.C(N)([S-])=S.C(N)([S-])=S Chemical compound C(N)([S-])=S.[Zn+2].[Zn+2].C=C.C(N)([S-])=S.C(N)([S-])=S.C(N)([S-])=S IXBUVPSMFSZIRK-UHFFFAOYSA-J 0.000 description 1
- 239000005752 Copper oxychloride Substances 0.000 description 1
- YVGGHNCTFXOJCH-UHFFFAOYSA-N DDT Chemical compound C1=CC(Cl)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(Cl)C=C1 YVGGHNCTFXOJCH-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241000556984 Neonectria galligena Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- CSKNSYBAZOQPLR-UHFFFAOYSA-N benzenesulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC=C1 CSKNSYBAZOQPLR-UHFFFAOYSA-N 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 description 1
- DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 1
- 229950006824 dieldrin Drugs 0.000 description 1
- NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 description 1
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- JTEDVYBZBROSJT-UHFFFAOYSA-N indole-3-butyric acid Chemical compound C1=CC=C2C(CCCC(=O)O)=CNC2=C1 JTEDVYBZBROSJT-UHFFFAOYSA-N 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 229960002809 lindane Drugs 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000006396 nitration reaction Methods 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003513 tertiary aromatic amines Chemical class 0.000 description 1
- 238000009736 wetting Methods 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
- C07C205/07—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms
- C07C205/11—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to carbon atoms of six-membered aromatic rings
- C07C205/12—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to carbon atoms of six-membered aromatic rings the six-membered aromatic ring or a condensed ring system containing that ring being substituted by halogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR786142A FR74927E (fr) | 1959-02-09 | 1959-02-09 | Produit fongicide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE565945A true BE565945A (enrdf_load_stackoverflow) |
Family
ID=8711000
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE537420D BE537420A (enrdf_load_stackoverflow) | 1959-02-09 | ||
| BE565945D BE565945A (enrdf_load_stackoverflow) | 1959-02-09 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE537420D BE537420A (enrdf_load_stackoverflow) | 1959-02-09 |
Country Status (2)
| Country | Link |
|---|---|
| BE (2) | BE565945A (enrdf_load_stackoverflow) |
| FR (2) | FR1142278A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3177225A (en) * | 1962-06-26 | 1965-04-06 | Fundamental Res Company | 1, 2, 3, 4, 5, 6-hexachloro-7-nitronaphthalene and certain derivatives thereof |
-
0
- BE BE537420D patent/BE537420A/fr unknown
- BE BE565945D patent/BE565945A/fr unknown
-
1956
- 1956-03-03 FR FR1142278D patent/FR1142278A/fr not_active Expired
-
1959
- 1959-02-09 FR FR786142A patent/FR74927E/fr not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3177225A (en) * | 1962-06-26 | 1965-04-06 | Fundamental Res Company | 1, 2, 3, 4, 5, 6-hexachloro-7-nitronaphthalene and certain derivatives thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| BE537420A (enrdf_load_stackoverflow) | |
| FR74927E (fr) | 1961-03-03 |
| FR1142278A (fr) | 1957-09-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0087375B1 (fr) | Nouveaux dérivés du cyano-2 benzimidazole, leur préparation et leur utilisation comme fongicides et acaricides | |
| BE1006426A6 (fr) | Procede de preparation de la n-methyl-3-phenyl-3-[4-(trifluoromethyl)-phenoxy]-propylamine et de ses sels d'addition d'acide. | |
| CH627431A5 (fr) | Procede de preparation de nouveaux acides cyclopropane carboxyliques comportant un groupement polyhalogene. | |
| CH651030A5 (fr) | Polymethylene-4,5 isothiazoline-4 ones-3, le procede de preparation et compositions antibacteriennes, antifongiques ou anti-acne les contenant. | |
| FR2559150A1 (fr) | Nouveaux derives du cyano-2 benzimidazole, leur preparation et leur utilisation comme fongicides | |
| EP0069033B1 (fr) | Herbicides à fonction amide et ester dérivés de la pyridine ainsi que leur procédé de préparation et leur application | |
| BE565945A (enrdf_load_stackoverflow) | ||
| DD221456A5 (de) | Verfahren zur herstellung von neuen derivaten von hydroxylamine | |
| LU84091A1 (fr) | Derives n-carbamoyl d'isothiazolo-(5,4b)pyridine one-3,leur procede de preparation et leurs utilisations comme agents bactericides et fongicides | |
| EP0112262A1 (fr) | Nouveaux dérivés de la benzylcarbamoylpyridine | |
| LU85292A1 (fr) | Procede pour la preparation de 1,8-dihydroxy-10-acyl-9-anthrones,en particulier pour une utilisation dans le traitement du psoriasis | |
| Bloom et al. | Nitroacetamidation of styrenes | |
| EP0069001B1 (fr) | Procédé de préparation de dérivés de la tétrahydro-5,6,7,7a 4H-thiéno (3,2-C) pyridinone-2 | |
| US3394145A (en) | Nu-(3, 4-dichlorophenyl) maleimide | |
| EP0181826A1 (fr) | Nouveaux dérivés du cyano-2 benzimidazole, leur préparation et leur utilisation comme fongicides et acaricides | |
| EP0017602B1 (fr) | Dérivés de la phényl-2-pyrone-4, procédé pour leur préparation et leur utilisation comme fongicides | |
| US2861918A (en) | Amine salts | |
| EP0122206A2 (fr) | Nouveaux dérivés de cyano-2 imidazopyridine, leur préparation et leur utilisation comme fongicides | |
| FR2566769A1 (fr) | Agent de fluoration de composes organiques notamment de composes acetyleniques, leur procede de preparation et leur utilisation dans les reactions d'addition ou de substitution nucleophile | |
| CH660365A5 (fr) | Benzoate de tricyclohexyletain comme derive organique de l'etain. | |
| CH630601A5 (en) | Cyclopropanecarboxylic acids containing a polyhalogenated group | |
| FR2737085A1 (fr) | Associations insecticides d'un oxime carbamate avec un insecticide a groupe pyrazole ou phenylimidazole | |
| US2733268A (en) | L-chloro-z | |
| EP0249567A2 (fr) | Dérivés propargyloxybenzènes, leur préparation et compositions fongicides les contenant | |
| FR2558155A1 (fr) | Derives du phenoxy-benzaldehyde, procede pour leur preparation et composition fongicide les contenant |