BE455970A - - Google Patents
Info
- Publication number
- BE455970A BE455970A BE455970DA BE455970A BE 455970 A BE455970 A BE 455970A BE 455970D A BE455970D A BE 455970DA BE 455970 A BE455970 A BE 455970A
- Authority
- BE
- Belgium
- Prior art keywords
- products
- compounds
- addition
- process according
- inorganic
- Prior art date
Links
- 238000000034 method Methods 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- BZWKPZBXAMTXNQ-UHFFFAOYSA-N sulfurocyanidic acid Chemical compound OS(=O)(=O)C#N BZWKPZBXAMTXNQ-UHFFFAOYSA-N 0.000 claims description 5
- 230000001274 anti-cryptogamic effect Effects 0.000 claims description 4
- 230000000749 insecticidal effect Effects 0.000 claims description 3
- 239000002917 insecticide Substances 0.000 claims description 3
- 239000005995 Aluminium silicate Substances 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000000853 adhesive Substances 0.000 claims description 2
- 230000001070 adhesive effect Effects 0.000 claims description 2
- 235000012211 aluminium silicate Nutrition 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 238000009835 boiling Methods 0.000 claims description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 239000000454 talc Substances 0.000 claims description 2
- 229910052623 talc Inorganic materials 0.000 claims description 2
- 238000009736 wetting Methods 0.000 claims description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001923 cyclic compounds Chemical class 0.000 description 2
- 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 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229960002809 lindane Drugs 0.000 description 2
- 241000288904 Lemur Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 description 1
- 230000002238 attenuated effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- ZNNZYHKDIALBAK-UHFFFAOYSA-M potassium thiocyanate Chemical compound [K+].[S-]C#N ZNNZYHKDIALBAK-UHFFFAOYSA-M 0.000 description 1
- 230000036515 potency Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 101150017423 sctL gene Proteins 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C331/00—Derivatives of thiocyanic acid or of isothiocyanic acid
- C07C331/02—Thiocyanates
- C07C331/06—Thiocyanates having sulfur atoms of thiocyanate groups bound to carbon atoms of rings other than six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE455970A true BE455970A (cs) |
Family
ID=109760
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE455970D BE455970A (cs) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE455970A (cs) |
-
0
- BE BE455970D patent/BE455970A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CH652385A5 (fr) | 5-(2-facultativement substitue-4-trifluoromethyl-6-facultativement substitue-phenoxy)-2-nitro, -halo ou -cyano-phenylcarbonyle alpha substitues-oximes et derives carbonyles correspondants. | |
| BE662268A (cs) | ||
| CH631444A5 (fr) | Composes 5-trifluoromethylpyridine 2-substitues et procede pour la preparation de ceux-ci. | |
| FR2961205A1 (fr) | Procede de preparation de composes esteramides | |
| CA1121832A (fr) | Procede de preparation stereoselectif de pheromones sexuelles | |
| BE455970A (cs) | ||
| CH642614A5 (fr) | Procede de preparation d'acides trichlorophenoxyalcanoiques et de leurs derives exempts de dibenzo-p-dioxines chlorees. | |
| LU85292A1 (fr) | Procede pour la preparation de 1,8-dihydroxy-10-acyl-9-anthrones,en particulier pour une utilisation dans le traitement du psoriasis | |
| BE574921A (cs) | ||
| EP3844144B1 (fr) | Nouveaux composes tetrazenes fonctionnalises | |
| BE633027A (cs) | ||
| RU2711963C1 (ru) | Способ получения регулятора роста растений N,N-ди(2-гидроксиэтил)-N,N-диметиламмония диметилфосфата | |
| FR2602766A1 (fr) | Composes dichlorotrifluoromethylnitrotoluenes et procede de preparation d'aminotrifluoromethyltoluenes a partir de ces composes | |
| JPS608285A (ja) | 芳香剤として有用なジヒドロフラン誘導体を含有する香料組成物 | |
| BE629779A (cs) | ||
| EP2580185A1 (fr) | Procede de preparation de composes estaramides | |
| EP0012390A2 (fr) | Procédé pour la préparation de la muscone et composés pyranniques intermédiaires | |
| EP0216659A1 (fr) | Nouveaux halogénoformiates de dihalogéno-2,2 vinyle, leur procédé de préparation et leurs applications | |
| EP0135444A1 (fr) | Dérivés pyroglutamiques, procédé de préparation, intermédiaires de synthèse de préparation de ceux-ci et compositions antibactérien ou antifongiques, cosmetiques ou pharmaceutiques | |
| EP0325072B1 (fr) | Perfectionnement à la préparation d'alcools tertiaires et secondaires par l'action d'un composé organo-manganeux sur un composé porteur de groupe carbonyle | |
| BE649569A (cs) | ||
| BE883210A (fr) | Acides et esters de 5-(4-trifluoromethyl-6-phenoxy-2-nitro (ou -halo ou -cyano)-phenyl-carbonyles, -oximes et-carboxy-oximes a activite herbicide | |
| EP0070995A1 (fr) | Procédé pour la préparation de cétones cycloaliphatiques polyinsaturées | |
| CH314008A (fr) | Procédé de préparation de thréo-1-p-nitrophényl-2-acylamidopropane-1,3-diols | |
| BE625731A (cs) |