FI56304C - Fungicid - Google Patents
Fungicid Download PDFInfo
- Publication number
- FI56304C FI56304C FI1802/74A FI180274A FI56304C FI 56304 C FI56304 C FI 56304C FI 1802/74 A FI1802/74 A FI 1802/74A FI 180274 A FI180274 A FI 180274A FI 56304 C FI56304 C FI 56304C
- Authority
- FI
- Finland
- Prior art keywords
- dithiol
- thione
- methyl
- product
- compounds
- Prior art date
Links
- 230000000855 fungicidal effect Effects 0.000 title description 6
- 239000000417 fungicide Substances 0.000 title description 5
- 239000000047 product Substances 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 7
- 241000233866 Fungi Species 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 5
- 238000005987 sulfurization reaction Methods 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 241001061127 Thione Species 0.000 description 4
- 150000004662 dithiols Chemical class 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000003071 parasitic effect Effects 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241001465180 Botrytis Species 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 230000000843 anti-fungal effect Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- KXPHJGWRCICEDH-UHFFFAOYSA-N 1-sulfanylidene-3h-dithiole Chemical group S=S1SCC=C1 KXPHJGWRCICEDH-UHFFFAOYSA-N 0.000 description 1
- PTHBKNSHSCMKBV-UHFFFAOYSA-N 4,6,8-trihydroxy-3-(2-hydroxyethyl)-2,3-dihydronaphtho[2,3-f][1]benzofuran-5,10-dione Chemical compound O=C1C2=CC(O)=CC(O)=C2C(=O)C2=C1C=C1OCC(CCO)C1=C2O PTHBKNSHSCMKBV-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 241000586542 Aonidiella citrina Species 0.000 description 1
- 241000123650 Botrytis cinerea Species 0.000 description 1
- 241000222356 Coriolus Species 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 241000222355 Trametes versicolor Species 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- -1 ethyl formyl Chemical group 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 150000002730 mercury Chemical class 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- PTHBKNSHSCMKBV-ZETCQYMHSA-N versicol Natural products OCC[C@H]1COc2cc3C(=O)c4cc(O)cc(O)c4C(=O)c3c(O)c12 PTHBKNSHSCMKBV-ZETCQYMHSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D339/00—Heterocyclic compounds containing rings having two sulfur atoms as the only ring hetero atoms
- C07D339/02—Five-membered rings
- C07D339/04—Five-membered rings having the hetero atoms in positions 1 and 2, e.g. lipoic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7324301A FR2236416B1 (de) | 1973-06-27 | 1973-06-27 | |
| FR7324301 | 1973-06-27 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI180274A7 FI180274A7 (de) | 1974-12-28 |
| FI56304B FI56304B (fi) | 1979-09-28 |
| FI56304C true FI56304C (fi) | 1980-01-10 |
Family
ID=9121938
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI1802/74A FI56304C (fi) | 1973-06-27 | 1974-06-12 | Fungicid |
Country Status (13)
| Country | Link |
|---|---|
| AT (1) | AT334688B (de) |
| BE (1) | BE816917A (de) |
| BR (1) | BR7405284D0 (de) |
| DE (1) | DE2430802C3 (de) |
| DK (1) | DK136932B (de) |
| FI (1) | FI56304C (de) |
| FR (1) | FR2236416B1 (de) |
| GB (1) | GB1447131A (de) |
| IT (1) | IT1049292B (de) |
| LU (1) | LU70415A1 (de) |
| NL (1) | NL7408694A (de) |
| NO (1) | NO139657C (de) |
| SE (1) | SE419692B (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1301177C (en) * | 1986-03-05 | 1992-05-19 | Itaru Yamamoto | Process of producing novel 1,2-dithiol-3-thione derivative |
-
1973
- 1973-06-27 FR FR7324301A patent/FR2236416B1/fr not_active Expired
-
1974
- 1974-06-10 SE SE7407591A patent/SE419692B/xx unknown
- 1974-06-12 FI FI1802/74A patent/FI56304C/fi active
- 1974-06-19 GB GB2721374A patent/GB1447131A/en not_active Expired
- 1974-06-25 NO NO742311A patent/NO139657C/no unknown
- 1974-06-25 AT AT526074A patent/AT334688B/de not_active IP Right Cessation
- 1974-06-26 BE BE145937A patent/BE816917A/xx not_active IP Right Cessation
- 1974-06-26 IT IT51762/74A patent/IT1049292B/it active
- 1974-06-26 LU LU70415*A patent/LU70415A1/xx unknown
- 1974-06-26 DK DK344674AA patent/DK136932B/da not_active IP Right Cessation
- 1974-06-27 DE DE2430802A patent/DE2430802C3/de not_active Expired
- 1974-06-27 BR BR5284/74A patent/BR7405284D0/pt unknown
- 1974-06-27 NL NL7408694A patent/NL7408694A/xx not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| GB1447131A (en) | 1976-08-25 |
| DE2430802B2 (de) | 1979-06-07 |
| SE7407591L (de) | 1974-12-30 |
| AT334688B (de) | 1976-01-25 |
| DK136932B (da) | 1977-12-19 |
| DE2430802C3 (de) | 1980-01-31 |
| FI56304B (fi) | 1979-09-28 |
| DK136932C (de) | 1978-07-03 |
| FR2236416A1 (de) | 1975-02-07 |
| DK344674A (de) | 1975-02-24 |
| NO742311L (de) | 1975-01-20 |
| IT1049292B (it) | 1981-01-20 |
| DE2430802A1 (de) | 1975-01-16 |
| NO139657B (no) | 1979-01-15 |
| NO139657C (no) | 1979-04-25 |
| LU70415A1 (de) | 1975-08-20 |
| BR7405284D0 (pt) | 1975-01-07 |
| ATA526074A (de) | 1976-05-15 |
| NL7408694A (de) | 1974-12-31 |
| FR2236416B1 (de) | 1977-12-23 |
| BE816917A (fr) | 1974-12-27 |
| SE419692B (sv) | 1981-08-24 |
| FI180274A7 (de) | 1974-12-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Gibert et al. | Availability and reactivity of concentrated dimethyldioxirane solutions in solvents other than acetone | |
| JPS58148864A (ja) | 2−シアノベンズイミダゾ−ル誘導体、該誘導体の製造方法ならびに該誘導体の殺菌剤及び殺ダニ剤としての使用 | |
| US4116665A (en) | Method of regulating the growth of aquatic weeds with pyridine derivatives | |
| FI56304C (fi) | Fungicid | |
| Gregory | Synthesis of novel organic nitrate esters: guanylate cyclase activation and tissue relaxation | |
| JP2985604B2 (ja) | 包接化合物 | |
| Owen et al. | 94. Small-ring heterocyclic compounds. Part II. Reactions of aliphatic glycidic esters with thiourea and with thioacetic acid | |
| PL116564B1 (en) | Microbicide | |
| CA1059530A (en) | Combating fungi with n-chloroacetyl-n-(2,6-di-substituted phenyl)-alanine esters | |
| JP4112916B2 (ja) | 農園芸用殺菌剤組成物およびカーバメート殺菌剤の効力増強剤 | |
| US5578622A (en) | Isothiazole derivatives and their uses | |
| RU2220973C2 (ru) | Замещенное пятичленное гетероциклическое соединение, фунгицидная композиция, содержащая его, способ его получения, способ борьбы с заболеваниями растений | |
| SU577933A3 (ru) | Гербицидное средство | |
| US4215127A (en) | Substituted 1-phenoxy-1-triazolyl-2-butanone compounds and their use as fungicides | |
| US3069253A (en) | Alkenyl pyridinium quaternary compounds as defoliants | |
| US2835626A (en) | Process for the production of new pyridazine derivatives and their use as fungicides | |
| WO1997002271A1 (en) | Pesticidal compounds | |
| CA1051777A (en) | Fungicidal agent | |
| RU1825792C (ru) | 1-Фенил-4(5)-(2,4-дихлорбензоилоксиметил)-1,2,3-триазол, обладающий фунгицидным действием | |
| US3890340A (en) | Preparation of 2,1-benzisothiazoles | |
| US2786798A (en) | Anhydrides of mucochloric acid | |
| GB1595261A (en) | Method of regulating the growth of aquatic weeds with pyridine derivatives | |
| EP0017602A1 (de) | 2-Phenyl-4-pyron-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Fungizide | |
| US3478043A (en) | 3-oxa-tricyclo(4.2.1.0**2,5)nonanes | |
| IE48779B1 (en) | 1,4-oxaza-spirohydrocarbon derivatives,their preparation and plant protecting compositions containing them |