DE1120802B - Schaedlingsbekaempfungsmittel - Google Patents
SchaedlingsbekaempfungsmittelInfo
- Publication number
- DE1120802B DE1120802B DEF28426A DEF0028426A DE1120802B DE 1120802 B DE1120802 B DE 1120802B DE F28426 A DEF28426 A DE F28426A DE F0028426 A DEF0028426 A DE F0028426A DE 1120802 B DE1120802 B DE 1120802B
- Authority
- DE
- Germany
- Prior art keywords
- dodecylamino
- crotonic acid
- acid
- radical
- optionally substituted
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 241000607479 Yersinia pestis Species 0.000 title description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 239000000575 pesticide Substances 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical class OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 2
- 150000002429 hydrazines Chemical class 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 2
- -1 β - dodecylamino - crotonic acid - (N - methyl anilide) Chemical compound 0.000 description 19
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 12
- 239000002253 acid Substances 0.000 description 11
- 239000004480 active ingredient Substances 0.000 description 11
- 206010061217 Infestation Diseases 0.000 description 10
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 8
- 150000003931 anilides Chemical class 0.000 description 4
- 230000000855 fungicidal effect Effects 0.000 description 4
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 description 3
- 230000000895 acaricidal effect Effects 0.000 description 3
- BZSYYMAHNJHZCB-QHHAFSJGSA-N (e)-n-phenylbut-2-enamide Chemical compound C\C=C\C(=O)NC1=CC=CC=C1 BZSYYMAHNJHZCB-QHHAFSJGSA-N 0.000 description 2
- 241000239290 Araneae Species 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- 241000227653 Lycopersicon Species 0.000 description 2
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
- 241000233622 Phytophthora infestans Species 0.000 description 2
- 241001454293 Tetranychus urticae Species 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 description 2
- ILRSCQWREDREME-UHFFFAOYSA-N dodecanamide Chemical compound CCCCCCCCCCCC(N)=O ILRSCQWREDREME-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- FLLFKFMTRYRALL-ARQDHWQXSA-N (2r,3s,4r,5r)-2,3,4,5,6-pentahydroxy-n-methylhexanamide Chemical compound CNC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FLLFKFMTRYRALL-ARQDHWQXSA-N 0.000 description 1
- CNLIGAJKYMPHAH-SNAWJCMRSA-N (E)-N-[4-(dimethylamino)phenyl]but-2-enamide Chemical compound C\C=C\C(=O)NC1=CC=C(N(C)C)C=C1 CNLIGAJKYMPHAH-SNAWJCMRSA-N 0.000 description 1
- ZNHWWCWGJIPOGH-LNKIKWGQSA-N (E)-N-dodecylbut-2-enamide Chemical compound C(CCCCCCCCCCC)NC(\C=C\C)=O ZNHWWCWGJIPOGH-LNKIKWGQSA-N 0.000 description 1
- QAVGKCMDOKZSBK-NSCUHMNNSA-N (e)-1-morpholin-4-ylbut-2-en-1-one Chemical compound C\C=C\C(=O)N1CCOCC1 QAVGKCMDOKZSBK-NSCUHMNNSA-N 0.000 description 1
- YFNVWPJYFXSPNZ-XNWCZRBMSA-N (e)-n,n-diphenylbut-2-enamide Chemical compound C=1C=CC=CC=1N(C(=O)/C=C/C)C1=CC=CC=C1 YFNVWPJYFXSPNZ-XNWCZRBMSA-N 0.000 description 1
- TXOLUMKJHRULMF-DUXPYHPUSA-N (e)-n-(3-cyanophenyl)but-2-enamide Chemical compound C\C=C\C(=O)NC1=CC=CC(C#N)=C1 TXOLUMKJHRULMF-DUXPYHPUSA-N 0.000 description 1
- AXOQYJNUYGHXKO-QHHAFSJGSA-N (e)-n-cyclohexylbut-2-enamide Chemical compound C\C=C\C(=O)NC1CCCCC1 AXOQYJNUYGHXKO-QHHAFSJGSA-N 0.000 description 1
- JMZRZEXRYJUHEB-UHFFFAOYSA-N 2-carbamothioylsulfanylethyl carbamodithioate;zinc Chemical compound [Zn].NC(=S)SCCSC(N)=S JMZRZEXRYJUHEB-UHFFFAOYSA-N 0.000 description 1
- OQEBBZSWEGYTPG-UHFFFAOYSA-N 3-aminobutanoic acid Chemical class CC(N)CC(O)=O OQEBBZSWEGYTPG-UHFFFAOYSA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- 241001388466 Bruchus rufimanus Species 0.000 description 1
- 241000122098 Ephestia kuehniella Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 241000233626 Plasmopara Species 0.000 description 1
- 150000004729 acetoacetic acid derivatives Chemical class 0.000 description 1
- QWCKQJZIFLGMSD-UHFFFAOYSA-N alpha-aminobutyric acid Chemical class CCC(N)C(O)=O QWCKQJZIFLGMSD-UHFFFAOYSA-N 0.000 description 1
- JPYQFYIEOUVJDU-UHFFFAOYSA-N beclamide Chemical compound ClCCC(=O)NCC1=CC=CC=C1 JPYQFYIEOUVJDU-UHFFFAOYSA-N 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 1
- 125000005594 diketone group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- KFFYUXCTXYMGPP-KTKRTIGZSA-N ethyl (Z)-3-benzamidobut-2-enoate Chemical compound CCOC(=O)\C=C(\C)NC(=O)C1=CC=CC=C1 KFFYUXCTXYMGPP-KTKRTIGZSA-N 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- UHANVDZCDNSILX-UHFFFAOYSA-N n-phenylbutanamide Chemical compound CCCC(=O)NC1=CC=CC=C1 UHANVDZCDNSILX-UHFFFAOYSA-N 0.000 description 1
- 230000003151 ovacidal effect Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/55—Acids; Esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE590804D BE590804A (en, 2012) | 1959-05-13 | ||
NL251479D NL251479A (en, 2012) | 1959-05-13 | ||
DEF28426A DE1120802B (de) | 1959-05-13 | 1959-05-13 | Schaedlingsbekaempfungsmittel |
DEF29826A DE1137896B (de) | 1959-05-13 | 1959-11-11 | Pilzbekaempfungsmittel |
CH504760A CH386170A (de) | 1959-05-13 | 1960-05-03 | Schädlingsbekämpfungsmittel |
US28215A US3096237A (en) | 1959-05-13 | 1960-05-11 | Methods of combating mites and fungi |
GB16676/60A GB914040A (en) | 1959-05-13 | 1960-05-11 | New pesticidally-active compounds and new pest control agents |
FR827157A FR1258523A (fr) | 1959-05-13 | 1960-05-13 | Agents antiparasitaires |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF28426A DE1120802B (de) | 1959-05-13 | 1959-05-13 | Schaedlingsbekaempfungsmittel |
DEF29826A DE1137896B (de) | 1959-05-13 | 1959-11-11 | Pilzbekaempfungsmittel |
Publications (1)
Publication Number | Publication Date |
---|---|
DE1120802B true DE1120802B (de) | 1961-12-28 |
Family
ID=25974309
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEF28426A Pending DE1120802B (de) | 1959-05-13 | 1959-05-13 | Schaedlingsbekaempfungsmittel |
DEF29826A Pending DE1137896B (de) | 1959-05-13 | 1959-11-11 | Pilzbekaempfungsmittel |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEF29826A Pending DE1137896B (de) | 1959-05-13 | 1959-11-11 | Pilzbekaempfungsmittel |
Country Status (6)
Country | Link |
---|---|
US (1) | US3096237A (en, 2012) |
BE (1) | BE590804A (en, 2012) |
CH (1) | CH386170A (en, 2012) |
DE (2) | DE1120802B (en, 2012) |
GB (1) | GB914040A (en, 2012) |
NL (1) | NL251479A (en, 2012) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1191629B (de) * | 1962-03-16 | 1965-04-22 | Basf Ag | Fungizide Mittel |
RU2141760C1 (ru) * | 1993-12-12 | 1999-11-27 | Агроджин, Лтд. | Способ защиты растений от грибковой инфекции (варианты) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE618643A (en, 2012) * | 1961-06-07 | 1900-01-01 | ||
US3330624A (en) * | 1964-06-05 | 1967-07-11 | Allied Chem | Preparation of pyrosulfuryl fluoride and by-products |
US3666810A (en) * | 1969-06-11 | 1972-05-30 | Lubrizol Corp | Novel n-3-aminoalkyl amides, polymers thereof, and method for their preparation |
IT8049659A0 (it) * | 1979-09-14 | 1980-09-12 | Amf Inc | Procedimento ed apparecchiatura per produrre una cucitura a macchina con cambiamento di direzione |
US5041545A (en) * | 1989-04-06 | 1991-08-20 | Atochem North America, Inc. | 2-hydroxybenzophenone hydrazides and derivatives thereof |
EP2488496A1 (en) * | 2009-10-16 | 2012-08-22 | Bayer CropScience AG | Aminopropenoates as fungicides |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2588969A (en) * | 1949-11-26 | 1952-03-11 | Eastman Kodak Co | Certain acylamino-acrylates and-crotonates as insecticides |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2273849A (en) * | 1940-04-01 | 1942-02-24 | Albert K Epstein | Parasiticidal material |
US2268206A (en) * | 1940-04-01 | 1941-12-30 | Albert K Epstein | Parasiticidal material |
US2323391A (en) * | 1940-06-29 | 1943-07-06 | Carbide & Carbon Chem Corp | Beta-amino acid amides and method of making same |
US2290174A (en) * | 1940-10-04 | 1942-07-21 | Albert K Epstein | Bactericidal, germicidal, and antiseptic materials |
US2368195A (en) * | 1941-09-15 | 1945-01-30 | Dow Chemical Co | Insecticidal compositions |
US2505681A (en) * | 1946-06-28 | 1950-04-25 | Geigy Ag J R | Pharmaceutical preparation for relieving itch and killing acaridae |
US2507110A (en) * | 1946-07-11 | 1950-05-09 | Du Pont | Color forming photographic development utilizing amino-nu-hydrocarbon substituted beta-amino-acrylamide couplers |
US2945883A (en) * | 1953-05-20 | 1960-07-19 | Farmaceutici Italia | Process for converting optically active aminodiols into racemic aminodiols by oxidation followed by racemization |
GB809286A (en) * | 1954-07-05 | 1959-02-18 | Hoechst Ag | Basically substituted butyric acid anilides and process for their manufacture |
US2938053A (en) * | 1955-12-29 | 1960-05-24 | Monsanto Chemicals | Amino acid analogues |
US2959518A (en) * | 1956-06-11 | 1960-11-08 | Philips Corp | Fungicides |
US2898373A (en) * | 1956-09-24 | 1959-08-04 | Hoffmann La Roche | Stabilization of panthenol |
US2941002A (en) * | 1956-11-06 | 1960-06-14 | Hoechst Ag | Beta-hydroxy carboxylic acid amides substituted at the nitrogen atom |
-
0
- BE BE590804D patent/BE590804A/xx unknown
- NL NL251479D patent/NL251479A/xx unknown
-
1959
- 1959-05-13 DE DEF28426A patent/DE1120802B/de active Pending
- 1959-11-11 DE DEF29826A patent/DE1137896B/de active Pending
-
1960
- 1960-05-03 CH CH504760A patent/CH386170A/de unknown
- 1960-05-11 US US28215A patent/US3096237A/en not_active Expired - Lifetime
- 1960-05-11 GB GB16676/60A patent/GB914040A/en not_active Expired
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2588969A (en) * | 1949-11-26 | 1952-03-11 | Eastman Kodak Co | Certain acylamino-acrylates and-crotonates as insecticides |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1191629B (de) * | 1962-03-16 | 1965-04-22 | Basf Ag | Fungizide Mittel |
RU2141760C1 (ru) * | 1993-12-12 | 1999-11-27 | Агроджин, Лтд. | Способ защиты растений от грибковой инфекции (варианты) |
US6075051A (en) * | 1993-12-12 | 2000-06-13 | Agrogene Ltd. | Method for protecting plants from fungal infection |
Also Published As
Publication number | Publication date |
---|---|
CH386170A (de) | 1964-12-31 |
DE1137896B (de) | 1962-10-11 |
GB914040A (en) | 1962-12-28 |
BE590804A (en, 2012) | |
US3096237A (en) | 1963-07-02 |
NL251479A (en, 2012) |
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