GB894614A - Chemotherapeutic compositions for controlling plant rusts - Google Patents
Chemotherapeutic compositions for controlling plant rustsInfo
- Publication number
- GB894614A GB894614A GB4362359A GB4362359A GB894614A GB 894614 A GB894614 A GB 894614A GB 4362359 A GB4362359 A GB 4362359A GB 4362359 A GB4362359 A GB 4362359A GB 894614 A GB894614 A GB 894614A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- carbazate
- ethyl
- phenyl
- chlorophenyl
- 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.)
- Expired
Links
- 230000000973 chemotherapeutic effect Effects 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- 241000221535 Pucciniales Species 0.000 title 1
- -1 hydroxy- Chemical class 0.000 abstract 12
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- 125000002950 monocyclic group Chemical group 0.000 abstract 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 abstract 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 abstract 2
- 125000002723 alicyclic group Chemical group 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- JPUCYDHPJLXDSO-UHFFFAOYSA-N ethyl n-(3-chloroanilino)carbamate Chemical compound CCOC(=O)NNC1=CC=CC(Cl)=C1 JPUCYDHPJLXDSO-UHFFFAOYSA-N 0.000 abstract 2
- JPXNCCJPSUCIRB-UHFFFAOYSA-N ethyl n-(n-ethylanilino)carbamate Chemical compound CCOC(=O)NN(CC)C1=CC=CC=C1 JPXNCCJPSUCIRB-UHFFFAOYSA-N 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- LWPSWQRLDLUTJR-UHFFFAOYSA-N phenyl N-(N-ethylanilino)carbamate Chemical compound C(C)N(NC(=O)OC1=CC=CC=C1)C1=CC=CC=C1 LWPSWQRLDLUTJR-UHFFFAOYSA-N 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000005544 phthalimido group Chemical group 0.000 abstract 2
- 125000003367 polycyclic group Chemical group 0.000 abstract 2
- XXMJLNVCUYMLPE-UHFFFAOYSA-N propan-2-yl n-(3-chloroanilino)carbamate Chemical compound CC(C)OC(=O)NNC1=CC=CC(Cl)=C1 XXMJLNVCUYMLPE-UHFFFAOYSA-N 0.000 abstract 2
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 abstract 2
- XDIRYDXFENKDQO-UHFFFAOYSA-N (4-chlorophenyl) N-(4-bromoanilino)carbamate Chemical compound BrC1=CC=C(C=C1)NNC(=O)OC1=CC=C(C=C1)Cl XDIRYDXFENKDQO-UHFFFAOYSA-N 0.000 abstract 1
- CPTQOIBHYXAUCX-UHFFFAOYSA-N 2-chloroethyl n-(2-chloroanilino)carbamate Chemical compound ClCCOC(=O)NNC1=CC=CC=C1Cl CPTQOIBHYXAUCX-UHFFFAOYSA-N 0.000 abstract 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- ZZLCFHIKESPLTH-UHFFFAOYSA-N 4-Methylbiphenyl Chemical compound C1=CC(C)=CC=C1C1=CC=CC=C1 ZZLCFHIKESPLTH-UHFFFAOYSA-N 0.000 abstract 1
- ZMKZXBSLXSSREJ-UHFFFAOYSA-N 4-chlorobut-2-ynyl n-anilinocarbamate Chemical compound ClCC#CCOC(=O)NNC1=CC=CC=C1 ZMKZXBSLXSSREJ-UHFFFAOYSA-N 0.000 abstract 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 abstract 1
- 239000005909 Kieselgur Substances 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000013543 active substance Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000005036 alkoxyphenyl group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract 1
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical compound OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 abstract 1
- 125000000068 chlorophenyl group Chemical group 0.000 abstract 1
- 239000004927 clay Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 1
- 239000003995 emulsifying agent Substances 0.000 abstract 1
- 230000001804 emulsifying effect Effects 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- KVYKYLSBMZUJQM-UHFFFAOYSA-N ethyl n-(3-nitroanilino)carbamate Chemical compound CCOC(=O)NNC1=CC=CC([N+]([O-])=O)=C1 KVYKYLSBMZUJQM-UHFFFAOYSA-N 0.000 abstract 1
- NLKPMUCEBRRUOK-UHFFFAOYSA-N ethyl n-anilinocarbamate Chemical compound CCOC(=O)NNC1=CC=CC=C1 NLKPMUCEBRRUOK-UHFFFAOYSA-N 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- 125000005059 halophenyl group Chemical group 0.000 abstract 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 abstract 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 239000003350 kerosene Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- WFJRIDQGVSJLLH-UHFFFAOYSA-N methyl n-aminocarbamate Chemical compound COC(=O)NN WFJRIDQGVSJLLH-UHFFFAOYSA-N 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 abstract 1
- DCCAZPDNTKRXLQ-UHFFFAOYSA-N phenyl N-(2,4-dichloroanilino)carbamate Chemical compound ClC1=C(C=CC(=C1)Cl)NNC(=O)OC1=CC=CC=C1 DCCAZPDNTKRXLQ-UHFFFAOYSA-N 0.000 abstract 1
- WSDQIHATCCOMLH-UHFFFAOYSA-N phenyl n-(3,5-dichlorophenyl)carbamate Chemical compound ClC1=CC(Cl)=CC(NC(=O)OC=2C=CC=CC=2)=C1 WSDQIHATCCOMLH-UHFFFAOYSA-N 0.000 abstract 1
- 125000004344 phenylpropyl group Chemical group 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 1
- 239000000454 talc Substances 0.000 abstract 1
- 229910052623 talc Inorganic materials 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000000080 wetting agent Substances 0.000 abstract 1
Classifications
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US678520A US2920994A (en) | 1957-08-16 | 1957-08-16 | Compositions and methods for controlling plant rust |
| DE1959S0066362 DE1114056B (de) | 1959-12-23 | 1959-12-21 | Mittel zur Bekaempfung von Pflanzenrost |
| GB4362359A GB894614A (en) | 1959-12-23 | 1959-12-23 | Chemotherapeutic compositions for controlling plant rusts |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB4362359A GB894614A (en) | 1959-12-23 | 1959-12-23 | Chemotherapeutic compositions for controlling plant rusts |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB894614A true GB894614A (en) | 1962-04-26 |
Family
ID=10429593
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4362359A Expired GB894614A (en) | 1957-08-16 | 1959-12-23 | Chemotherapeutic compositions for controlling plant rusts |
Country Status (2)
| Country | Link |
|---|---|
| DE (1) | DE1114056B (enrdf_load_stackoverflow) |
| GB (1) | GB894614A (enrdf_load_stackoverflow) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT180765B (de) * | 1952-01-08 | 1955-01-10 | Bataafsche Petroleum | Mittel zur Bekämpfung von Schädlingen |
| USRE24960E (en) * | 1954-09-24 | 1961-04-04 | Co-nhxnh- |
-
1959
- 1959-12-21 DE DE1959S0066362 patent/DE1114056B/de active Granted
- 1959-12-23 GB GB4362359A patent/GB894614A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE1114056B (de) | 1961-09-21 |
| DE1114056C2 (enrdf_load_stackoverflow) | 1962-04-05 |
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