BE624760A - - Google Patents
Info
- Publication number
- BE624760A BE624760A BE624760DA BE624760A BE 624760 A BE624760 A BE 624760A BE 624760D A BE624760D A BE 624760DA BE 624760 A BE624760 A BE 624760A
- Authority
- BE
- Belgium
- Prior art keywords
- halogen
- compounds
- alkyl
- hydrogen
- radicals
- Prior art date
Links
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 241000233866 Fungi Species 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 150000001450 anions Chemical class 0.000 claims description 3
- 239000000417 fungicide Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 150000002825 nitriles Chemical class 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
- -1 nitro, hydroxyl Chemical group 0.000 claims 2
- 125000002252 acyl group Chemical group 0.000 claims 1
- 125000004442 acylamino group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 239000013543 active substance Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 8
- 235000010582 Pisum sativum Nutrition 0.000 description 4
- 240000004713 Pisum sativum Species 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 241000228245 Aspergillus niger Species 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241000118205 Ovicides Species 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002361 compost Substances 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE624760A true BE624760A (enrdf_load_stackoverflow) |
Family
ID=196303
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE624760D BE624760A (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE624760A (enrdf_load_stackoverflow) |
-
0
- BE BE624760D patent/BE624760A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0070219B1 (fr) | Compositions herbicides à base de dérivés d'amino-4 chloro-6 alkylthio-5 pyrimidine et de dérivés de la dinitro-2,6 aniline et procédé de traitement des cultures à l'aide desdites compositions | |
| FR2521141A1 (fr) | Nouveaux derives du cyano-2 benzimidazole, leur preparation et leur utilisation comme fongicides | |
| FR2559150A1 (fr) | Nouveaux derives du cyano-2 benzimidazole, leur preparation et leur utilisation comme fongicides | |
| BE624760A (enrdf_load_stackoverflow) | ||
| FR2572401A1 (fr) | Nouveaux derives du cyano-2 benzimidazole, leur preparation et leur utilisation comme fongicides et acaricides | |
| CH643825A5 (fr) | Procede de preparation d'un sel d'acide mineral de cysteamine. | |
| BE636245A (enrdf_load_stackoverflow) | ||
| BE818849A (fr) | Derives de cyclohexane | |
| BE675278A (enrdf_load_stackoverflow) | ||
| US3639604A (en) | Compositions containing an organic thiocyanate and 2-hydroxy alkyl esters of organic thiosulfonic acids and processes of utilizing th same | |
| FR2502615A2 (fr) | Agents de chelation et leurs chelates | |
| BE875594A (fr) | Procede de preparation de cetazines, et produits ainsi obtenus | |
| BE823198A (fr) | Derives organosulfures du tetrachlorobenzonitrile | |
| BE563583A (enrdf_load_stackoverflow) | ||
| BE565945A (enrdf_load_stackoverflow) | ||
| FR2617844A1 (fr) | Compositions fongicides a base de derives nicotiniques. nouveaux derives nicotiniques et leur preparation | |
| FR2544587A1 (fr) | Compositions fongicides contenant des 5-tertio-butyl-1,3,4-thiadiazole-2-yl-urees substituees | |
| FR2537839A1 (fr) | Application comme facteurs de croissance des vegetaux de l'o-phenyl hydroxylamine et de certains de ses derives | |
| BE458858A (enrdf_load_stackoverflow) | ||
| BE475273A (enrdf_load_stackoverflow) | ||
| BE634998A (enrdf_load_stackoverflow) | ||
| BE470133A (enrdf_load_stackoverflow) | ||
| BE564238A (enrdf_load_stackoverflow) | ||
| CH417851A (fr) | Procédé de préparation d'un sel d'addition de la blasticidine-S | |
| FR2516748A1 (fr) | Compositions herbicides a base de derives d'amino-4 chloro-6 alkylthio-5 pyrimidine et de pyridate, et procede de traitement des cultures a l'aide desdites compositions |