DE2430802C3 - Fungizid, enthaltend als Wirkstoff eine Verbindung mit dem Dithiol-1,2thion-3-ring sowie dessen Verwendung - Google Patents

Fungizid, enthaltend als Wirkstoff eine Verbindung mit dem Dithiol-1,2thion-3-ring sowie dessen Verwendung

Info

Publication number: DE2430802C3
Authority: DE; Germany
Prior art keywords: dithiol; thione; active ingredient; ring; compound
Prior art date: 1973-06-27
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

Application number

DE2430802A

Other languages

German (de)

English (en)

Other versions

DE2430802B2 (de

DE2430802A1 (de

Inventor

Bernard Lyon Buathier

Jose Caluire Moyne

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

RHONE-PROGIL COURBEVOIE HAUTS-DE- SEINE (FRANKREICH)

Original Assignee

RHONE-PROGIL COURBEVOIE HAUTS-DE- SEINE (FRANKREICH)

Priority date (The priority date 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 date listed.)

1973-06-27

Filing date

1974-06-27

Publication date

1980-01-31

1974-06-27 Application filed by RHONE-PROGIL COURBEVOIE HAUTS-DE- SEINE (FRANKREICH) filed Critical RHONE-PROGIL COURBEVOIE HAUTS-DE- SEINE (FRANKREICH)

1975-01-16 Publication of DE2430802A1 publication Critical patent/DE2430802A1/de

1979-06-07 Publication of DE2430802B2 publication Critical patent/DE2430802B2/de

1980-01-31 Application granted granted Critical

1980-01-31 Publication of DE2430802C3 publication Critical patent/DE2430802C3/de

Status Expired legal-status Critical Current

Links

150000001875 compounds Chemical class 0.000 title claims description 10
230000000855 fungicidal effect Effects 0.000 title claims description 8
239000000417 fungicide Substances 0.000 title claims description 8
239000004480 active ingredient Substances 0.000 title claims description 5
239000000047 product Substances 0.000 description 14
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
239000013543 active substance Substances 0.000 description 5
238000000034 method Methods 0.000 description 5
229910052717 sulfur Inorganic materials 0.000 description 5
239000011593 sulfur Substances 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
241000233866 Fungi Species 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
238000003786 synthesis reaction Methods 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
241000123650 Botrytis cinerea Species 0.000 description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
239000013078 crystal Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000000203 mixture Substances 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
239000008096 xylene Substances 0.000 description 3
235000001674 Agaricus brunnescens Nutrition 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
239000012043 crude product Substances 0.000 description 2
-1 ethyl formyl Chemical group 0.000 description 2
150000002430 hydrocarbons Chemical group 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
229910052753 mercury Inorganic materials 0.000 description 2
CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 2
238000001953 recrystallisation Methods 0.000 description 2
238000005987 sulfurization reaction Methods 0.000 description 2
239000012808 vapor phase Substances 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
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
241000222356 Coriolus Species 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-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
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
241000222355 Trametes versicolor Species 0.000 description 1
239000008272 agar Substances 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
150000004662 dithiols Chemical class 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000009472 formulation Methods 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
239000010985 leather Substances 0.000 description 1
238000004519 manufacturing process Methods 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
238000004321 preservation Methods 0.000 description 1
238000010992 reflux Methods 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
125000001424 substituent group Chemical group 0.000 description 1
150000003464 sulfur compounds Chemical class 0.000 description 1
239000004753 textile 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
239000000080 wetting agent Substances 0.000 description 1
239000002023 wood Substances 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)

DE2430802A 1973-06-27 1974-06-27 Fungizid, enthaltend als Wirkstoff eine Verbindung mit dem Dithiol-1,2thion-3-ring sowie dessen Verwendung Expired DE2430802C3 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
FR7324301A FR2236416B1 (fr)	1973-06-27	1973-06-27

Publications (3)

Publication Number	Publication Date
DE2430802A1 DE2430802A1 (de)	1975-01-16
DE2430802B2 DE2430802B2 (de)	1979-06-07
DE2430802C3 true DE2430802C3 (de)	1980-01-31

Family

ID=9121938

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE2430802A Expired DE2430802C3 (de)	1973-06-27	1974-06-27	Fungizid, enthaltend als Wirkstoff eine Verbindung mit dem Dithiol-1,2thion-3-ring sowie dessen Verwendung

Country Status (13)

Country	Link
AT (1)	AT334688B (fr)
BE (1)	BE816917A (fr)
BR (1)	BR7405284D0 (fr)
DE (1)	DE2430802C3 (fr)
DK (1)	DK136932B (fr)
FI (1)	FI56304C (fr)
FR (1)	FR2236416B1 (fr)
GB (1)	GB1447131A (fr)
IT (1)	IT1049292B (fr)
LU (1)	LU70415A1 (fr)
NL (1)	NL7408694A (fr)
NO (1)	NO139657C (fr)
SE (1)	SE419692B (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1301177C (fr) *	1986-03-05	1992-05-19	Itaru Yamamoto	Procede pour la production d'un nouveau derive 1,2-dithiol-3-thione

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 AT AT526074A patent/AT334688B/de not_active IP Right Cessation
- 1974-06-25 NO NO742311A patent/NO139657C/no unknown
- 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
- 1974-06-26 BE BE145937A patent/BE816917A/fr 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
NL7408694A (fr)	1974-12-31
FI56304B (fi)	1979-09-28
FI180274A7 (fr)	1974-12-28
FR2236416B1 (fr)	1977-12-23
FR2236416A1 (fr)	1975-02-07
AT334688B (de)	1976-01-25
LU70415A1 (fr)	1975-08-20
DK136932C (fr)	1978-07-03
GB1447131A (en)	1976-08-25
SE7407591L (fr)	1974-12-30
DE2430802B2 (de)	1979-06-07
DK344674A (fr)	1975-02-24
FI56304C (fi)	1980-01-10
ATA526074A (de)	1976-05-15
BR7405284D0 (pt)	1975-01-07
SE419692B (sv)	1981-08-24
NO139657C (no)	1979-04-25
BE816917A (fr)	1974-12-27
DE2430802A1 (de)	1975-01-16
NO742311L (fr)	1975-01-20
NO139657B (no)	1979-01-15
DK136932B (da)	1977-12-19
IT1049292B (it)	1981-01-20

Legal Events

Date	Code	Title	Description
1980-01-31	C3	Grant after two publication steps (3rd publication)
1986-06-12	8339	Ceased/non-payment of the annual fee

Publication	Publication Date	Title
DE2406475C2 (de)	1983-04-28	5-Acetamido-2,4-dimethyltrifluormethansulfonanilid und dessen landwirtschaftlich geeignete Salze, Verfahren zur Herstellung dieser Verbindungen und diese Verbindungen enthaltende Mittel
DE3146309C2 (fr)	1990-11-08
DE2442706A1 (de)	1976-03-25	Substituierte imidazolderivate
DE1620353A1 (de)	1972-03-09	Verfahren zur Herstellung von Pyridylamiden
EP0003304B1 (fr)	1981-11-25	Procédé de préparation des 2,6-dialcoylanilines N-substituées
DE1445820B1 (de)	1970-03-19	Verfahren zur Herstellung von 2-Alkylamino-delta?-azacycloheptenen und deren Salzen
DE2430802B2 (de)	1979-06-07	Fungizid, enthaltend als Wirkstoff eine Verbindung mit dem Dithiol-Uthion-3-ring sowie dessen Verwendung
DE1593551C3 (de)	1974-10-17	N-substituierte O- eckige Klammer auf 3-Alkanoylaminophenyl eckige Klammer zu -carbamate und dieselben enthaltende Herbizide
DE1254147B (de)	1967-11-16	Verfahren zur Herstellung von insektizid wirksamen 1, 9, 10, 11, 12, 12-Hexachloro-tricyclo-[7, 2, 1, 0]-dodeka-3, 6, 10-trien
DE1542892C3 (fr)	1975-03-13
DE2453210C3 (de)	1979-11-22	Bekämpfung von Pilzen der Gattung Hehmnthosporium mit Dimethyipyrazolylbenzimidazol
DD143999A5 (de)	1980-09-24	Pflanzenschutzmittel
DE1567046A1 (de)	1970-05-27	Parasitizides,insbesondere fungizides Mittel
DE2200325A1 (de)	1973-07-12	3-(2-phenylisopropyl)-harnstoffderivate
AT203799B (de)	1959-06-10	Fungizide Mittel
DE2030464C3 (de)	1978-09-14	bis-Formamidverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung phytopathogener Pilze
DE1098281B (de)	1961-01-26	Fungicides Mittel
DE974569C (de)	1961-03-02	Schaedlingsbekaempfungsmittel
DE1542913C3 (de)	1976-07-29	4,4-Bipyrldyliumsalze
DE1593676C3 (de)	1976-06-10	Benzhydrylcarbamate, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Schädlingsbekämpfungsmittel
DE1162629B (de)	1964-02-06	Nematocide Mischungen
DE1518025A1 (de)	1969-02-06	Schaedlingsbekaempfungsmittel mit insektizider Wirkung
DE2548898A1 (de)	1976-05-06	Benzothiazolderivate, verfahren zu ihrer herstellung und ihre verwendung als herbizide
DE975092C (de)	1961-08-10	Schaedlingsbekaempfungsmittel
AT339662B (de)	1977-11-10	Insektizide, akarizide und nematizide mittel