BE734818A - - Google Patents
Info
- Publication number
- BE734818A BE734818A BE734818DA BE734818A BE 734818 A BE734818 A BE 734818A BE 734818D A BE734818D A BE 734818DA BE 734818 A BE734818 A BE 734818A
- Authority
- BE
- Belgium
- Prior art keywords
- sep
- group
- carbon atoms
- desc
- clms page
- Prior art date
Links
- 125000004432 carbon atom Chemical group C* 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 18
- 125000004429 atom Chemical group 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 11
- 238000002360 preparation method Methods 0.000 claims description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 239000013543 active substance Substances 0.000 claims description 6
- 239000000460 chlorine Substances 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000000853 cresyl group Chemical group C1(=CC=C(C=C1)C)* 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 238000006873 Coates reaction Methods 0.000 claims 1
- 241000490229 Eucephalus Species 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 150000005690 diesters Chemical class 0.000 claims 1
- 238000004821 distillation Methods 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 150000002391 heterocyclic compounds Chemical class 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- OCYSGIYOVXAGKQ-UHFFFAOYSA-N hydron;3-[1-hydroxy-2-(methylamino)ethyl]phenol;chloride Chemical compound Cl.CNCC(O)C1=CC=CC(O)=C1 OCYSGIYOVXAGKQ-UHFFFAOYSA-N 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 239000002304 perfume Substances 0.000 claims 1
- 101150069548 ppan gene Proteins 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- 150000004072 triols Chemical class 0.000 claims 1
- 239000000243 solution Substances 0.000 description 17
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 10
- 150000002148 esters Chemical class 0.000 description 8
- 239000000470 constituent Substances 0.000 description 7
- 238000001704 evaporation Methods 0.000 description 7
- 230000007062 hydrolysis Effects 0.000 description 7
- 238000006460 hydrolysis reaction Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 6
- 230000008020 evaporation Effects 0.000 description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 6
- 229920002554 vinyl polymer Polymers 0.000 description 6
- 230000002209 hydrophobic effect Effects 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 101100178984 Caenorhabditis elegans hyl-2 gene Proteins 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 239000002917 insecticide Substances 0.000 description 4
- 241000283014 Dama Species 0.000 description 3
- 101150110390 Slc10a6 gene Proteins 0.000 description 3
- 239000011149 active material Substances 0.000 description 3
- JNSGIVNNHKGGRU-JYRVWZFOSA-N diethoxyphosphinothioyl (2z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetate Chemical compound CCOP(=S)(OCC)OC(=O)C(=N/OC)\C1=CSC(N)=N1 JNSGIVNNHKGGRU-JYRVWZFOSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N ethyl acetate Substances CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- -1 hydroxyl compound Chemical class 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 241000132092 Aster Species 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003570 air Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000749 insecticidal effect Effects 0.000 description 2
- UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 2
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- 235000013616 tea Nutrition 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 2
- 239000012808 vapor phase Substances 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- NFLGAXVYCFJBMK-RKDXNWHRSA-N (+)-isomenthone Natural products CC(C)[C@H]1CC[C@@H](C)CC1=O NFLGAXVYCFJBMK-RKDXNWHRSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- ZCLZVWYFTIREFE-UHFFFAOYSA-N 4-benzyl-1-methyl-3,6-dihydro-2h-pyridine;hydrochloride Chemical compound Cl.C1N(C)CCC(CC=2C=CC=CC=2)=C1 ZCLZVWYFTIREFE-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 101100272279 Beauveria bassiana Beas gene Proteins 0.000 description 1
- 241001674044 Blattodea Species 0.000 description 1
- 101100377790 Caenorhabditis elegans aat-6 gene Proteins 0.000 description 1
- 101100495270 Caenorhabditis elegans cdc-26 gene Proteins 0.000 description 1
- 101100508416 Caenorhabditis elegans ifd-1 gene Proteins 0.000 description 1
- 101100521097 Caenorhabditis elegans pri-1 gene Proteins 0.000 description 1
- 101100227198 Campylobacter jejuni flaA gene Proteins 0.000 description 1
- 241000631130 Chrysophyllum argenteum Species 0.000 description 1
- 241000543381 Cliftonia monophylla Species 0.000 description 1
- 102100029411 Cytochrome c oxidase assembly factor 8 Human genes 0.000 description 1
- 101710113468 Cytochrome c oxidase assembly factor 8 Proteins 0.000 description 1
- 241000723298 Dicentrarchus labrax Species 0.000 description 1
- 101100536354 Drosophila melanogaster tant gene Proteins 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 241000861223 Issus Species 0.000 description 1
- NFLGAXVYCFJBMK-UHFFFAOYSA-N Menthone Chemical compound CC(C)C1CCC(C)CC1=O NFLGAXVYCFJBMK-UHFFFAOYSA-N 0.000 description 1
- 101150034459 Parpbp gene Proteins 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- VRDIULHPQTYCLN-UHFFFAOYSA-N Prothionamide Chemical compound CCCC1=CC(C(N)=S)=CC=N1 VRDIULHPQTYCLN-UHFFFAOYSA-N 0.000 description 1
- OVZITGHGWBXFEA-UHFFFAOYSA-N Pyridinitril Chemical compound ClC1=NC(Cl)=C(C#N)C(C=2C=CC=CC=2)=C1C#N OVZITGHGWBXFEA-UHFFFAOYSA-N 0.000 description 1
- 235000014443 Pyrus communis Nutrition 0.000 description 1
- 101150098533 SOST gene Proteins 0.000 description 1
- 101100210375 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) WWM1 gene Proteins 0.000 description 1
- 101100297821 Schizosaccharomyces pombe (strain 972 / ATCC 24843) pli1 gene Proteins 0.000 description 1
- 241000383403 Solen Species 0.000 description 1
- 241000708948 Solva Species 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 241000613130 Tima Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- IPBVNPXQWQGGJP-UHFFFAOYSA-N acetic acid phenyl ester Natural products CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 description 1
- BILVKKQEHOFANR-UHFFFAOYSA-N acetic acid;octyl acetate Chemical compound CC(O)=O.CCCCCCCCOC(C)=O BILVKKQEHOFANR-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 235000001053 badasse Nutrition 0.000 description 1
- 210000000481 breast Anatomy 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- WOAFDHWYKSOANX-UHFFFAOYSA-N diisopropyl methylphosphonate Chemical compound CC(C)OP(C)(=O)OC(C)C WOAFDHWYKSOANX-UHFFFAOYSA-N 0.000 description 1
- 239000012636 effector Substances 0.000 description 1
- OYFJQPXVCSSHAI-QFPUQLAESA-N enalapril maleate Chemical compound OC(=O)\C=C/C(O)=O.C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](CCC1)C(O)=O)CC1=CC=CC=C1 OYFJQPXVCSSHAI-QFPUQLAESA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 235000009606 lavandin Nutrition 0.000 description 1
- 244000056931 lavandin Species 0.000 description 1
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 1
- 229930007503 menthone Natural products 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 201000002266 mite infestation Diseases 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229940023569 palmate Drugs 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 229940049953 phenylacetate Drugs 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- 101150103950 priS gene Proteins 0.000 description 1
- ZMRUPTIKESYGQW-UHFFFAOYSA-N propranolol hydrochloride Chemical compound [H+].[Cl-].C1=CC=C2C(OCC(O)CNC(C)C)=CC=CC2=C1 ZMRUPTIKESYGQW-UHFFFAOYSA-N 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 101150042187 trmJ gene Proteins 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/18—Vapour or smoke emitting compositions with delayed or sustained release
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/113—Esters of phosphoric acids with unsaturated acyclic alcohols
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Pest Control & Pesticides (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Toxicology (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR156025 | 1968-06-21 | ||
| FR6903313A FR2031909A6 (en) | 1969-02-12 | 1969-02-12 | Insecticidal (thio)phosphoric ester compsns. |
| BE734818 | 1969-06-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE734818A true BE734818A (enrdf_load_html_response) | 1969-12-19 |
Family
ID=27159308
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE734818D BE734818A (enrdf_load_html_response) | 1968-06-21 | 1969-06-19 |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE734818A (enrdf_load_html_response) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2091953A1 (enrdf_load_html_response) * | 1970-01-09 | 1971-01-21 | Ciba Geigy |
-
1969
- 1969-06-19 BE BE734818D patent/BE734818A/fr unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2091953A1 (enrdf_load_html_response) * | 1970-01-09 | 1971-01-21 | Ciba Geigy |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5670159A (en) | Fragrance-containing cosmetic gelatin capsule | |
| Muallem et al. | Electrolyte transport across the basolateral membrane of the parietal cells. | |
| CH667993A5 (de) | Pharmazeutische formulierungen zur behandlung von gedaechtnisstoerungen. | |
| Hökfelt et al. | Histochemical support for a dopaminergic mechanism in the dendrites of certain periglomerular cells in the rat olfactory bulb | |
| Devarakonda et al. | Effect of polyamidoamine (PAMAM) dendrimers on the in vitro release of water-insoluble nifedipine from aqueous gels | |
| FR2775898A1 (fr) | Eau structuree dans des compositions cosmetiques | |
| Astrachan et al. | Spinal modulation of the acoustic startle response: The role of norepinephrine, serotonin, and dopamine. | |
| BR112021011509A2 (pt) | Composições e métodos relativos a moléculas de canabinoide aniônicas | |
| Zierler | Increased muscle permeability to aldolase produced by depolarization and by metabolic inhibitors | |
| US3875301A (en) | Useful tetraalkyl diamides in the treatment of poison ivy | |
| BE734818A (enrdf_load_html_response) | ||
| CN101541324A (zh) | 医药组合物 | |
| Nabeshima et al. | Effects of 5-HT2 receptor antagonist on cycloheximide-induced amnesia in mice | |
| Dethier et al. | The electron microscopy of chemosensory hairs | |
| Diamond et al. | High affinity transport of 2-deoxyglucose in isolated synaptic nerve endings | |
| Toshitaka et al. | Protection with phencyclidine against inactivation of 5-HT2 receptors by sulfhydryl-modifying reagents | |
| Sander et al. | Inhibitory effect of terbinafine on reactive oxygen species (ROS) generation by Candida albicans: Hemmender Einfluss von Terbinafin auf die Bildung reaktiver Sauerstoffspezies von Candida albicans | |
| EP0029790B1 (fr) | Nouveau médicament à base d'aspirine et d'heptaminol | |
| Christensen et al. | Mathematical model for in vitro drug release from controlled release dosage forms applied to propoxyphene hydrochloride pellets | |
| Meller et al. | Differential dose-and time-dependent effects of molindone on dopamine neurons of rat brain: mediation by irreversible inhibition of monoamine oxidase. | |
| Aizawa et al. | Effects of thapsigahgin, an intracellular CA2+ pump inhibitor, on insulin release by rat pancreatic B-cell | |
| JPH02196718A (ja) | 外用液剤 | |
| Ballantyne | Eye irritancy potential of diethylene glycol monobutyl ether | |
| JPH06502873A (ja) | 発香組成物 | |
| Montanari | Parole et stratégies de communication aux limites de l’humain |