IL37109A - Fungicidal composition containing 1,3-bis(-3-alkoxycarbonyl-2-thioureido)benzene and another ingredient - Google Patents
Fungicidal composition containing 1,3-bis(-3-alkoxycarbonyl-2-thioureido)benzene and another ingredientInfo
- Publication number
- IL37109A IL37109A IL37109A IL3710971A IL37109A IL 37109 A IL37109 A IL 37109A IL 37109 A IL37109 A IL 37109A IL 3710971 A IL3710971 A IL 3710971A IL 37109 A IL37109 A IL 37109A
- Authority
- IL
- Israel
- Prior art keywords
- bis
- thioureido
- fungicidal composition
- zinc
- composition according
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 30
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 title claims description 25
- 230000000855 fungicidal effect Effects 0.000 title claims description 20
- 239000004615 ingredient Substances 0.000 title description 2
- 206010039509 Scab Diseases 0.000 claims description 10
- 229940076134 benzene Drugs 0.000 claims description 10
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 9
- 208000015181 infectious disease Diseases 0.000 claims description 9
- 239000011701 zinc Substances 0.000 claims description 9
- 229910052725 zinc Inorganic materials 0.000 claims description 9
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 claims description 8
- 241000196324 Embryophyta Species 0.000 claims description 7
- 240000001987 Pyrus communis Species 0.000 claims description 5
- 235000014443 Pyrus communis Nutrition 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- -1 3-methoxycarbonyl-2-thioureido Chemical group 0.000 claims description 4
- MYODENLXTDMHTA-UHFFFAOYSA-N 7a-(trichloromethylsulfanyl)-4,5-dihydro-3ah-isoindole-1,3-dione Chemical compound C1=CCCC2C(=O)NC(=O)C21SC(Cl)(Cl)Cl MYODENLXTDMHTA-UHFFFAOYSA-N 0.000 claims description 4
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- URXFYTKCCMASJX-UHFFFAOYSA-N ethyl n-[[3-(ethoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC(NC(=S)NC(=O)OCC)=C1 URXFYTKCCMASJX-UHFFFAOYSA-N 0.000 claims description 4
- AWYFNIZYMPNGAI-UHFFFAOYSA-N ethylenebis(dithiocarbamic acid) Chemical class SC(=S)NCCNC(S)=S AWYFNIZYMPNGAI-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 claims description 4
- 241000317942 Venturia <ichneumonid wasp> Species 0.000 claims description 3
- 230000003213 activating effect Effects 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 230000000087 stabilizing effect Effects 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 claims description 2
- 239000005745 Captan Substances 0.000 claims description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 2
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 239000011717 all-trans-retinol Substances 0.000 claims description 2
- 235000019169 all-trans-retinol Nutrition 0.000 claims description 2
- 229940117949 captan Drugs 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 claims description 2
- 229920000940 maneb Polymers 0.000 claims description 2
- 229910052748 manganese Inorganic materials 0.000 claims description 2
- 239000011572 manganese Substances 0.000 claims description 2
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 claims 3
- 229960002447 thiram Drugs 0.000 claims 3
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 claims 2
- 241000237519 Bivalvia Species 0.000 claims 1
- 239000005764 Dithianon Substances 0.000 claims 1
- 239000005802 Mancozeb Substances 0.000 claims 1
- 239000005809 Metiram Substances 0.000 claims 1
- 239000005823 Propineb Substances 0.000 claims 1
- 239000005870 Ziram Substances 0.000 claims 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims 1
- 150000004056 anthraquinones Chemical class 0.000 claims 1
- LKNFSJXXGBLRAI-UHFFFAOYSA-N carbamodithioic acid;ethene Chemical class C=C.NC(S)=S.NC(S)=S LKNFSJXXGBLRAI-UHFFFAOYSA-N 0.000 claims 1
- 235000020639 clam Nutrition 0.000 claims 1
- PYZSVQVRHDXQSL-UHFFFAOYSA-N dithianon Chemical compound S1C(C#N)=C(C#N)SC2=C1C(=O)C1=CC=CC=C1C2=O PYZSVQVRHDXQSL-UHFFFAOYSA-N 0.000 claims 1
- WHDGWKAJBYRJJL-UHFFFAOYSA-K ferbam Chemical compound [Fe+3].CN(C)C([S-])=S.CN(C)C([S-])=S.CN(C)C([S-])=S WHDGWKAJBYRJJL-UHFFFAOYSA-K 0.000 claims 1
- 229920000257 metiram Polymers 0.000 claims 1
- VKJILRXHHIMQNS-UHFFFAOYSA-L n,n-dimethylcarbamothioate;iron(2+) Chemical compound [Fe+2].CN(C)C([O-])=S.CN(C)C([O-])=S VKJILRXHHIMQNS-UHFFFAOYSA-L 0.000 claims 1
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 claims 1
- 239000000417 fungicide Substances 0.000 description 10
- 235000011430 Malus pumila Nutrition 0.000 description 7
- 235000015103 Malus silvestris Nutrition 0.000 description 7
- 239000000843 powder Substances 0.000 description 6
- 241000220225 Malus Species 0.000 description 5
- 241000489964 Fusicladium Species 0.000 description 4
- ORWLTMJXWWQMEY-UHFFFAOYSA-N methyl N-[[3-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate Chemical compound COC(=O)NC(NC1=CC(=CC=C1)NC(=S)NC(=O)OC)=S ORWLTMJXWWQMEY-UHFFFAOYSA-N 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 235000013399 edible fruits Nutrition 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 244000141359 Malus pumila Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 241000228452 Venturia inaequalis Species 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 230000003389 potentiating effect Effects 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241001006642 Venturia pyrina Species 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 238000012271 agricultural production Methods 0.000 description 1
- 230000001274 anti-cryptogamic effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical class CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 230000008511 vegetative development Effects 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
- C07D235/30—Nitrogen atoms not forming part of a nitro radical
- C07D235/32—Benzimidazole-2-carbamic acids, unsubstituted or substituted; Esters thereof; Thio-analogues thereof
-
- 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material 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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT2642370 | 1970-06-23 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL37109A0 IL37109A0 (en) | 1971-08-25 |
| IL37109A true IL37109A (en) | 1974-12-31 |
Family
ID=11219454
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL37109A IL37109A (en) | 1970-06-23 | 1971-06-22 | Fungicidal composition containing 1,3-bis(-3-alkoxycarbonyl-2-thioureido)benzene and another ingredient |
| IL37108A IL37108A (en) | 1970-06-23 | 1971-06-22 | Fungicidal compositions containing 1-(butylcarbamoyl)-2-benzimidazole-n-methylcarbamate and another ingredient |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL37108A IL37108A (en) | 1970-06-23 | 1971-06-22 | Fungicidal compositions containing 1-(butylcarbamoyl)-2-benzimidazole-n-methylcarbamate and another ingredient |
Country Status (10)
| Country | Link |
|---|---|
| BE (2) | BE768891A (nl) |
| CA (1) | CA973091A (nl) |
| CH (2) | CH544492A (nl) |
| DE (2) | DE2131817A1 (nl) |
| FR (2) | FR2096430B3 (nl) |
| GB (1) | GB1349956A (nl) |
| IL (2) | IL37109A (nl) |
| NL (2) | NL7108571A (nl) |
| TR (2) | TR16787A (nl) |
| ZA (2) | ZA714032B (nl) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0236689A3 (de) * | 1986-01-27 | 1988-04-27 | Shell Internationale Researchmaatschappij B.V. | Fungizide Mittel |
| MD4077C1 (ro) * | 2010-01-18 | 2011-07-31 | Государственный Университет Молд0 | Procedeul de obţinere a acizilor N, N-dimetiltioureidobenzoici |
-
1971
- 1971-06-18 CA CA115,985A patent/CA973091A/en not_active Expired
- 1971-06-21 ZA ZA714032A patent/ZA714032B/xx unknown
- 1971-06-21 ZA ZA714031A patent/ZA714031B/xx unknown
- 1971-06-22 CH CH911571A patent/CH544492A/it not_active IP Right Cessation
- 1971-06-22 NL NL7108571A patent/NL7108571A/xx unknown
- 1971-06-22 CH CH911671A patent/CH544489A/it not_active IP Right Cessation
- 1971-06-22 IL IL37109A patent/IL37109A/en unknown
- 1971-06-22 NL NLAANVRAGE7108572,A patent/NL175254C/nl not_active IP Right Cessation
- 1971-06-22 FR FR7122605A patent/FR2096430B3/fr not_active Expired
- 1971-06-22 FR FR7122606A patent/FR2096431B1/fr not_active Expired
- 1971-06-22 IL IL37108A patent/IL37108A/en unknown
- 1971-06-23 BE BE768891A patent/BE768891A/xx unknown
- 1971-06-23 TR TR16787A patent/TR16787A/xx unknown
- 1971-06-23 DE DE19712131817 patent/DE2131817A1/de active Pending
- 1971-06-23 TR TR17188A patent/TR17188A/xx unknown
- 1971-06-23 DE DE19712131818 patent/DE2131818A1/de active Pending
- 1971-06-23 GB GB2950271A patent/GB1349956A/en not_active Expired
- 1971-06-23 BE BE768893A patent/BE768893A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA973091A (en) | 1975-08-19 |
| CH544489A (it) | 1973-11-30 |
| IL37108A0 (en) | 1971-08-25 |
| BE768893A (fr) | 1971-11-03 |
| GB1349956A (en) | 1974-04-10 |
| DE2131818A1 (de) | 1971-12-30 |
| NL7108572A (nl) | 1971-12-27 |
| FR2096430B3 (nl) | 1974-04-05 |
| FR2096431B1 (nl) | 1975-07-11 |
| TR16787A (tr) | 1973-05-01 |
| DE2131817A1 (de) | 1971-12-30 |
| CH544492A (it) | 1973-11-30 |
| ZA714032B (en) | 1972-02-23 |
| NL7108571A (nl) | 1971-12-27 |
| ZA714031B (en) | 1972-02-23 |
| NL175254C (nl) | 1984-10-16 |
| BE768891A (fr) | 1971-11-03 |
| IL37108A (en) | 1975-06-25 |
| IL37109A0 (en) | 1971-08-25 |
| FR2096430A3 (nl) | 1972-02-18 |
| FR2096431A1 (nl) | 1972-02-18 |
| TR17188A (tr) | 1974-04-25 |
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