CH645513A5 - N-aril-n-acil-3-ammino-ossazolidin-2-oni fungicidi. - Google Patents

N-aril-n-acil-3-ammino-ossazolidin-2-oni fungicidi. Download PDF

Info

Publication number: CH645513A5
Authority: CH; Switzerland
Prior art keywords: amino; compound according; oxazolidin; dimethylphenyl; compounds
Prior art date: 1979-09-07

Application number

CH660380A

Other languages

English (en)

Italian (it)

Inventor

Luigi Garlaschelli

Franco Gozzo

Luigi Mirenna

Original Assignee

Montedison Spa

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.)

1979-09-07

Filing date

1980-09-02

Publication date

1984-10-15

1980-09-02 Application filed by Montedison Spa filed Critical Montedison Spa

1984-10-15 Publication of CH645513A5 publication Critical patent/CH645513A5/it

Links

239000000417 fungicide Substances 0.000 title description 9
150000001875 compounds Chemical class 0.000 claims description 49
-1 C2-C5 alchemy Chemical group 0.000 claims description 20
241000196324 Embryophyta Species 0.000 claims description 18
230000000855 fungicidal effect Effects 0.000 claims description 17
208000015181 infectious disease Diseases 0.000 claims description 12
239000000203 mixture Substances 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 8
238000000034 method Methods 0.000 claims description 8
208000031888 Mycoses Diseases 0.000 claims description 7
241000233679 Peronosporaceae Species 0.000 claims description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
206010017533 Fungal infection Diseases 0.000 claims description 6
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 6
229910052736 halogen Inorganic materials 0.000 claims description 6
244000045561 useful plants Species 0.000 claims description 6
244000061176 Nicotiana tabacum Species 0.000 claims description 5
235000002637 Nicotiana tabacum Nutrition 0.000 claims description 5
125000005843 halogen group Chemical group 0.000 claims description 5
150000002367 halogens Chemical class 0.000 claims description 4
125000005842 heteroatom Chemical group 0.000 claims description 4
125000000623 heterocyclic group Chemical group 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
125000006729 (C2-C5) alkenyl group Chemical group 0.000 claims 2
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Chemical group C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims 1
125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims 1
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
231100000674 Phytotoxicity Toxicity 0.000 description 10
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
230000000694 effects Effects 0.000 description 8
ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 description 8
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
239000007787 solid Substances 0.000 description 6
239000000243 solution Substances 0.000 description 6
OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 5
125000002252 acyl group Chemical group 0.000 description 5
CIEXPHRYOLIQQD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-UHFFFAOYSA-N 0.000 description 5
230000001143 conditioned effect Effects 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
238000003756 stirring Methods 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
UFFBMTHBGFGIHF-UHFFFAOYSA-N 2,6-dimethylaniline Chemical group CC1=CC=CC(C)=C1N UFFBMTHBGFGIHF-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
238000001816 cooling Methods 0.000 description 3
230000002538 fungal effect Effects 0.000 description 3
238000011534 incubation Methods 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
238000010992 reflux Methods 0.000 description 3
239000002904 solvent Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
CCHJMGDYNLOYKM-UHFFFAOYSA-N (2,6-dimethylphenyl)hydrazine Chemical compound CC1=CC=CC(C)=C1NN CCHJMGDYNLOYKM-UHFFFAOYSA-N 0.000 description 2
235000001674 Agaricus brunnescens Nutrition 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
241000233866 Fungi Species 0.000 description 2
239000007832 Na2SO4 Substances 0.000 description 2
241001223281 Peronospora Species 0.000 description 2
241001281803 Plasmopara viticola Species 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
150000001266 acyl halides Chemical class 0.000 description 2
238000009472 formulation Methods 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
230000003032 phytopathogenic effect Effects 0.000 description 2
AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
229910052938 sodium sulfate Inorganic materials 0.000 description 2
235000011152 sodium sulphate Nutrition 0.000 description 2
239000000725 suspension Substances 0.000 description 2
238000005406 washing Methods 0.000 description 2
GOMPDUZAJUGIRG-NSOVKSMOSA-N (5S)-4-[2-(4-hydroxyphenyl)ethyl]-1-[4-[(2S)-1-[2-(4-hydroxyphenyl)ethyl]-5,6-dioxopiperazin-2-yl]butyl]-5-[(4-hydroxyphenyl)methyl]piperazine-2,3-dione Chemical compound C1=CC(O)=CC=C1CCN1C(=O)C(=O)NC[C@@H]1CCCCN1C(=O)C(=O)N(CCC=2C=CC(O)=CC=2)[C@@H](CC=2C=CC(O)=CC=2)C1 GOMPDUZAJUGIRG-NSOVKSMOSA-N 0.000 description 1
KYVBNYUBXIEUFW-UHFFFAOYSA-N 1,1,3,3-tetramethylguanidine Chemical compound CN(C)C(=N)N(C)C KYVBNYUBXIEUFW-UHFFFAOYSA-N 0.000 description 1
ZLCKDYMZBZNBMJ-UHFFFAOYSA-N 2-bromoethyl carbonochloridate Chemical compound ClC(=O)OCCBr ZLCKDYMZBZNBMJ-UHFFFAOYSA-N 0.000 description 1
JJKWHOSQTYYFAE-UHFFFAOYSA-N 2-methoxyacetyl chloride Chemical compound COCC(Cl)=O JJKWHOSQTYYFAE-UHFFFAOYSA-N 0.000 description 1
XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
ORILYTVJVMAKLC-UHFFFAOYSA-N Adamantane Natural products C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 description 1
101100516554 Caenorhabditis elegans nhr-5 gene Proteins 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
238000004566 IR spectroscopy Methods 0.000 description 1
QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical group C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
241001579016 Nanoa Species 0.000 description 1
241000582441 Peronospora tabacina Species 0.000 description 1
241000233626 Plasmopara Species 0.000 description 1
241001281802 Pseudoperonospora Species 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
240000003768 Solanum lycopersicum Species 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
240000000038 Ziziphus mauritiana Species 0.000 description 1
235000006545 Ziziphus mauritiana Nutrition 0.000 description 1
125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
125000002015 acyclic group Chemical group 0.000 description 1
239000000654 additive Substances 0.000 description 1
235000004279 alanine Nutrition 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
238000006482 condensation reaction Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
239000012954 diazonium Substances 0.000 description 1
150000001989 diazonium salts Chemical class 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
239000003480 eluent Substances 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
150000002332 glycine derivatives Chemical group 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
125000005179 haloacetyl group Chemical group 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
230000003641 microbiacidal effect Effects 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
230000003449 preventive effect Effects 0.000 description 1
125000003226 pyrazolyl group Chemical group 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
125000000714 pyrimidinyl group Chemical group 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000007363 ring formation reaction Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
235000011150 stannous chloride Nutrition 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
230000009897 systematic effect Effects 0.000 description 1
125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
125000001544 thienyl group Chemical group 0.000 description 1
AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/16—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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 to ring carbon atoms
- C07D263/18—Oxygen atoms
- C07D263/20—Oxygen atoms attached in position 2
- C07D263/26—Oxygen atoms attached in position 2 with hetero atoms or acyl radicals directly attached to the ring nitrogen atom
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Plural Heterocyclic Compounds (AREA)

CH660380A 1979-09-07 1980-09-02 N-aril-n-acil-3-ammino-ossazolidin-2-oni fungicidi. CH645513A5 (it)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT25538/79A IT1123564B (it)	1979-09-07	1979-09-07	N-aril-n-acil-3-ammino-ossazolidin-2-oni fungicidi

Publications (1)

Publication Number	Publication Date
CH645513A5 true CH645513A5 (it)	1984-10-15

Family

ID=11217010

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH660380A CH645513A5 (it)	1979-09-07	1980-09-02	N-aril-n-acil-3-ammino-ossazolidin-2-oni fungicidi.

Country Status (19)

Country	Link
JP (1)	JPS5655381A (fr)
AR (1)	AR228138A1 (fr)
AU (1)	AU545683B2 (fr)
BE (1)	BE885117A (fr)
BR (1)	BR8005645A (fr)
CA (1)	CA1203539A (fr)
CH (1)	CH645513A5 (fr)
CY (1)	CY1235A (fr)
DE (1)	DE3033161A1 (fr)
ES (1)	ES494856A0 (fr)
FR (1)	FR2464649A1 (fr)
GB (1)	GB2058071B (fr)
GR (1)	GR69955B (fr)
IL (1)	IL60950A (fr)
IT (1)	IT1123564B (fr)
KE (1)	KE3383A (fr)
NL (1)	NL8004962A (fr)
OA (1)	OA06743A (fr)
ZA (1)	ZA805450B (fr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3030026A1 (de) *	1980-08-08	1981-03-26	Sandoz-Patent-GmbH, 79539 Lörrach	Fungizide
DE3231605A1 (de) *	1981-02-05	1983-02-10	Sandoz Ag	Fungizide
DE3231606A1 (de) *	1981-02-09	1983-02-10	Sandoz Ag	Fungizide
NL8203049A (nl) *	1981-08-04	1983-03-01	Montedison Spa	Oxazolinonverbinding met fungicidewerking en werkwijzen voor het bereiden en toepassen van deze verbinding.
IT1168031B (it) *	1981-10-01	1987-05-20	Montedison Spa	Composti fungicidi
CH654979A5 (de) *	1982-01-26	1986-03-27	Sandoz Ag	Fungizide und ihre verwendung.
IT1152196B (it) *	1982-05-27	1986-12-31	Montedison Spa	Composto fungicida
GB8504181D0 (en) *	1985-02-19	1985-03-20	Sandoz Ltd	Fungicides
US4771063A (en) *	1985-06-06	1988-09-13	Montedison S.P.A	Fungicidally active N-(2-methyl-5-chlorophenyl)-N-methoxyacetyl-3-amino-1,3-oxazolidin-2-one
EP0284555A1 (fr) *	1987-03-12	1988-09-28	Ciba-Geigy Ag	Procédé de préparation de N-acyl-N-(oxazolidin-2-one-3-yl)-2,6-dialkyl-3-chloroanilines

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4097262A (en) *	1977-04-22	1978-06-27	E. I. Du Pont De Nemours And Company	Herbicidal acetamides
BE884661A (fr) *	1979-08-16	1981-02-09	Sandoz Sa	Nouvelles 3-amino-oxazolidine-2-ones, leur preparation et leur utilisation comme agents fongicides
CH646158A5 (en) *	1979-08-16	1984-11-15	Sandoz Ag	Fungicides
EP0030923A1 (fr) *	1979-12-18	1981-06-24	Ciba-Geigy Ag	3-(N-acyl-phénylamino)-2-oxazolidinones, procédé pour leur préparation et leur utilisation comme microbicides ou dans des agents microbicides
DE3030026A1 (de) *	1980-08-08	1981-03-26	Sandoz-Patent-GmbH, 79539 Lörrach	Fungizide

1979
- 1979-09-07 IT IT25538/79A patent/IT1123564B/it active
1980
- 1980-09-01 NL NL8004962A patent/NL8004962A/nl not_active Application Discontinuation
- 1980-09-02 IL IL60950A patent/IL60950A/xx unknown
- 1980-09-02 AU AU61949/80A patent/AU545683B2/en not_active Ceased
- 1980-09-02 CH CH660380A patent/CH645513A5/it not_active IP Right Cessation
- 1980-09-02 FR FR8018915A patent/FR2464649A1/fr active Granted
- 1980-09-03 JP JP12124080A patent/JPS5655381A/ja active Granted
- 1980-09-03 ZA ZA00805450A patent/ZA805450B/xx unknown
- 1980-09-03 DE DE19803033161 patent/DE3033161A1/de not_active Ceased
- 1980-09-04 BR BR8005645A patent/BR8005645A/pt not_active IP Right Cessation
- 1980-09-05 GR GR62813A patent/GR69955B/el unknown
- 1980-09-05 BE BE0/202012A patent/BE885117A/fr not_active IP Right Cessation
- 1980-09-05 CA CA000359647A patent/CA1203539A/fr not_active Expired
- 1980-09-06 ES ES494856A patent/ES494856A0/es active Granted
- 1980-09-08 GB GB8028922A patent/GB2058071B/en not_active Expired
- 1980-09-08 CY CY1235A patent/CY1235A/en unknown
- 1980-09-08 AR AR282439A patent/AR228138A1/es active
1981
- 1981-02-13 OA OA57326A patent/OA06743A/fr unknown
1984
- 1984-03-01 KE KE3383A patent/KE3383A/xx unknown

Also Published As

Publication number	Publication date
OA06743A (fr)	1982-06-30
AU6194980A (en)	1981-03-12
FR2464649B1 (fr)	1983-07-08
IL60950A (en)	1985-05-31
CA1203539A (fr)	1986-04-22
CY1235A (en)	1984-06-29
GB2058071B (en)	1983-11-09
JPH0240664B2 (fr)	1990-09-12
JPS5655381A (en)	1981-05-15
AR228138A1 (es)	1983-01-31
GB2058071A (en)	1981-04-08
IT7925538A0 (it)	1979-09-07
ES8106713A1 (es)	1981-09-01
IL60950A0 (en)	1980-11-30
ZA805450B (en)	1981-08-26
ES494856A0 (es)	1981-09-01
NL8004962A (nl)	1981-03-10
GR69955B (fr)	1982-07-22
BR8005645A (pt)	1981-03-17
IT1123564B (it)	1986-04-30
KE3383A (en)	1984-03-23
FR2464649A1 (fr)	1981-03-20
DE3033161A1 (de)	1981-04-02
AU545683B2 (en)	1985-07-25
BE885117A (fr)	1981-03-05

Legal Events

Date	Code	Title	Description
1994-05-31	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DD142042A5 (de)	1980-06-04	Verfahren zur herstellung von acylanilinen
DE3810080A1 (de)	1989-10-05	Trisubstituierte 1,3,5-triazin-2,4,6-trione
DE2741437C2 (fr)	1987-11-05
JPS6049638B2 (ja)	1985-11-02	カ−バメイト系殺虫剤
USRE27347E (en)	1972-04-25	Vii. chs
DE2843291A1 (de)	1979-04-12	Phenylisothiocyanate und deren salze, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE2628384A1 (de)	1978-04-13	Herbizide und fungizide mittel
JPH0240664B2 (fr)	1990-09-12
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DE2015527C3 (de)	1980-03-06	Cyanoalkylaldoximcarbamate und ihre Verwendung als Insektizide
PL117085B1 (en)	1981-07-31	Fungicide
CH648548A5 (it)	1985-03-29	Nuovi carbazati fungicidi.
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CA1160073A (fr)	1984-01-10	Acides ethane-sulfiniques substitues en beta, et leurs esters d'oxygene ou de soufre, utiles comme regulateurs de la croissance des plantes
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DE2112643B2 (de)	1980-06-12	Formanüdin-Denvate und sie enthaltende Mittel
EP0121344A2 (fr)	1984-10-10	Dérivés d'azolecarboxamides N,N-substituées utiles comme fongicides et nematocides
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