NO129602B - - Google Patents

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Info

Publication number: NO129602B
Authority: NO; Norway
Prior art keywords: plants; furan; alkyl; approx; soil
Prior art date: 1969-02-13

Application number

NO00466/70A

Other languages

English (en)

Norwegian (no)

Inventor

Robert Allan Davis

Bogislav Von Schmeling

Ethel Ellen Felauer

Marshall Kulka

Original Assignee

Uniroyal Inc

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.)

1969-02-13

Filing date

1970-02-10

Publication date

1974-05-06

1970-02-10 Application filed by Uniroyal Inc filed Critical Uniroyal Inc

1974-05-06 Publication of NO129602B publication Critical patent/NO129602B/no

Links

238000002360 preparation method Methods 0.000 claims description 32
125000000217 alkyl group Chemical group 0.000 claims description 8
230000000855 fungicidal effect Effects 0.000 claims description 8
239000004480 active ingredient Substances 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
229910052739 hydrogen Inorganic materials 0.000 claims description 6
150000002240 furans Chemical class 0.000 claims description 5
-1 lower- alkenyl Chemical group 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 3
150000002367 halogens Chemical class 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
JFSPBVWPKOEZCB-UHFFFAOYSA-N fenfuram Chemical compound O1C=CC(C(=O)NC=2C=CC=CC=2)=C1C JFSPBVWPKOEZCB-UHFFFAOYSA-N 0.000 claims description 2
ZWJNEYVWPYIKMB-UHFFFAOYSA-N methfuroxam Chemical compound CC1=C(C)OC(C)=C1C(=O)NC1=CC=CC=C1 ZWJNEYVWPYIKMB-UHFFFAOYSA-N 0.000 claims description 2
125000001624 naphthyl group Chemical group 0.000 claims description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
125000004076 pyridyl group Chemical group 0.000 claims description 2
125000000335 thiazolyl group Chemical group 0.000 claims description 2
125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
XEPBBUCQCXXTGR-UHFFFAOYSA-N 2,5-dimethyl-n-phenylfuran-3-carboxamide Chemical compound O1C(C)=CC(C(=O)NC=2C=CC=CC=2)=C1C XEPBBUCQCXXTGR-UHFFFAOYSA-N 0.000 claims 1
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 1
150000003931 anilides Chemical class 0.000 claims 1
241000196324 Embryophyta Species 0.000 description 33
150000001875 compounds Chemical class 0.000 description 23
201000010099 disease Diseases 0.000 description 23
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 23
239000002689 soil Substances 0.000 description 18
241000221577 Uromyces appendiculatus Species 0.000 description 16
GOLHZPOXCLTFRB-UHFFFAOYSA-N furan-3-carboxamide Chemical class NC(=O)C=1C=COC=1 GOLHZPOXCLTFRB-UHFFFAOYSA-N 0.000 description 14
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 12
239000003153 chemical reaction reagent Substances 0.000 description 9
208000015181 infectious disease Diseases 0.000 description 9
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 8
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
238000005507 spraying Methods 0.000 description 8
241000209140 Triticum Species 0.000 description 7
235000021307 Triticum Nutrition 0.000 description 7
238000005727 Friedel-Crafts reaction Methods 0.000 description 6
241000219146 Gossypium Species 0.000 description 6
238000013459 approach Methods 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
229920000742 Cotton Polymers 0.000 description 5
239000000417 fungicide Substances 0.000 description 5
239000000725 suspension Substances 0.000 description 5
230000009885 systemic effect Effects 0.000 description 5
241000209219 Hordeum Species 0.000 description 4
235000007340 Hordeum vulgare Nutrition 0.000 description 4
241000227653 Lycopersicon Species 0.000 description 4
244000046052 Phaseolus vulgaris Species 0.000 description 4
235000013339 cereals Nutrition 0.000 description 4
239000000243 solution Substances 0.000 description 4
239000007921 spray Substances 0.000 description 4
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
241000213004 Alternaria solani Species 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
241000233866 Fungi Species 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
241000540505 Puccinia dispersa f. sp. tritici Species 0.000 description 3
241000813090 Rhizoctonia solani Species 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
241000007070 Ustilago nuda Species 0.000 description 3
238000011161 development Methods 0.000 description 3
239000011521 glass Substances 0.000 description 3
150000002431 hydrogen Chemical class 0.000 description 3
238000011081 inoculation Methods 0.000 description 3
239000000203 mixture Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
208000024891 symptom Diseases 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
235000007688 Lycopersicon esculentum Nutrition 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
239000013504 Triton X-100 Substances 0.000 description 2
229920004890 Triton X-100 Polymers 0.000 description 2
125000003368 amide group Chemical group 0.000 description 2
229940053202 antiepileptics carboxamide derivative Drugs 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
235000012343 cottonseed oil Nutrition 0.000 description 2
230000008029 eradication Effects 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
238000000034 method Methods 0.000 description 2
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
244000052769 pathogen Species 0.000 description 2
230000001681 protective effect Effects 0.000 description 2
239000004576 sand Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
238000012360 testing method Methods 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
MNBYRCAFWIZFJM-UHFFFAOYSA-N 2,3,4-trimethylfuran Chemical compound CC1=COC(C)=C1C MNBYRCAFWIZFJM-UHFFFAOYSA-N 0.000 description 1
NMRDELHCVAOOPZ-UHFFFAOYSA-N 2,4-dimethyl-n-phenylfuran-3-carboxamide Chemical compound CC1=COC(C)=C1C(=O)NC1=CC=CC=C1 NMRDELHCVAOOPZ-UHFFFAOYSA-N 0.000 description 1
QNMLDXNBSGLHCA-UHFFFAOYSA-N 3-methyl-n-phenylfuran-2-carboxamide Chemical compound C1=COC(C(=O)NC=2C=CC=CC=2)=C1C QNMLDXNBSGLHCA-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
206010017533 Fungal infection Diseases 0.000 description 1
208000031888 Mycoses Diseases 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241001361634 Rhizoctonia Species 0.000 description 1
241000592344 Spermatophyta Species 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
229940098396 barley grain Drugs 0.000 description 1
238000009835 boiling Methods 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
TVFIYRKPCACCNL-UHFFFAOYSA-N furan-2-carboxamide Chemical class NC(=O)C1=CC=CO1 TVFIYRKPCACCNL-UHFFFAOYSA-N 0.000 description 1
229940059904 light mineral oil Drugs 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
XHVDWCKBZSFUDE-UHFFFAOYSA-N n-phenylfuran-2-carboxamide Chemical compound C=1C=COC=1C(=O)NC1=CC=CC=C1 XHVDWCKBZSFUDE-UHFFFAOYSA-N 0.000 description 1
239000006199 nebulizer Substances 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
238000003359 percent control normalization Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
238000006798 ring closing metathesis reaction Methods 0.000 description 1
RCIJACVHOIKRAP-UHFFFAOYSA-N sodium;1,4-dioctoxy-1,4-dioxobutane-2-sulfonic acid Chemical compound [Na+].CCCCCCCCOC(=O)CC(S(O)(=O)=O)C(=O)OCCCCCCCC RCIJACVHOIKRAP-UHFFFAOYSA-N 0.000 description 1
RTVVXRKGQRRXFJ-UHFFFAOYSA-N sodium;2-sulfobutanedioic acid Chemical compound [Na].OC(=O)CC(C(O)=O)S(O)(=O)=O RTVVXRKGQRRXFJ-UHFFFAOYSA-N 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
238000010998 test method Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011592 zinc chloride Substances 0.000 description 1
235000005074 zinc chloride Nutrition 0.000 description 1
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/01—Organic compounds containing nitrogen
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/012—Organic compounds containing sulfur
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D2203/00—Specified materials treated by the flotation agents; Specified applications
- B03D2203/003—Biotechnological applications, e.g. separation or purification of enzymes, hormones, vitamins, viruses

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (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)
Plural Heterocyclic Compounds (AREA)
Furan Compounds (AREA)

NO00466/70A 1969-02-13 1970-02-10 NO129602B (tr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US04/799,110 US3959481A (en)	1969-02-13	1969-02-13	Method of protecting plants from fungal diseases using furan-3-carboxamide derivatives

Publications (1)

Publication Number	Publication Date
NO129602B true NO129602B (tr)	1974-05-06

Family

ID=25175062

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO00466/70A NO129602B (tr)	1969-02-13	1970-02-10

Country Status (21)

Country	Link
US (1)	US3959481A (tr)
JP (1)	JPS5010376B1 (tr)
AT (1)	AT300460B (tr)
BE (1)	BE745864A (tr)
BR (1)	BR7016721D0 (tr)
CH (1)	CH557141A (tr)
CS (1)	CS188868B2 (tr)
DE (1)	DE2006471C2 (tr)
DK (1)	DK134232B (tr)
ES (1)	ES376540A1 (tr)
FR (1)	FR2033330B1 (tr)
GB (1)	GB1302410A (tr)
IL (1)	IL33881A (tr)
LU (1)	LU60344A1 (tr)
NL (1)	NL171957B (tr)
NO (1)	NO129602B (tr)
PL (1)	PL82624B1 (tr)
SE (1)	SE395590B (tr)
SU (1)	SU433664A3 (tr)
TR (1)	TR18587A (tr)
ZA (1)	ZA70862B (tr)

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DE2019535C3 (de) *	1970-04-23	1987-02-12	Basf Ag, 6700 Ludwigshafen	2,5-Dimethyl-furan-3-carbonsäure-cyclohexylamid und diese Verbindung enthaltende fungizide Mittel
GB1387652A (en) *	1972-05-10	1975-03-19	Shell Int Research	Process for preparing furan carboxamides
AR205189A1 (es) *	1974-04-02	1976-04-12	Ciba Geigy Ag	Derivados de n-(1"-metoxi-carboniletil)-n-(furan-(2") carbonil) 2-6-dimetilanilina utiles como agentes microbicidas menos para usos farmaceuticos y procedimiento para su obtencion
JPS52164960U (tr) *	1976-06-04	1977-12-14
DE2703023A1 (de) *	1977-01-26	1978-07-27	Basf Ag	Furanderivate
CH629939A5 (de) *	1977-03-29	1982-05-28	Ciba Geigy Ag	Mikrobizides mittel.
JPS5848560B2 (ja) *	1977-04-19	1983-10-28	住友化学工業株式会社	メチルｎ−アシルアントラニレ−ト誘導体、その製造法およびこれらを有効成分として含有する農園芸用殺菌剤
DE2823818C2 (de) *	1978-05-31	1987-01-15	HORA Landwirtschaftliche Betriebsmittel GmbH, 7867 Wehr	Saatgut-Beizmittel und deren Verwendung
DE2916853A1 (de) *	1979-04-26	1980-11-06	Wacker Chemie Gmbh	Fungizidkombination zur behandlung von getreidesaatgut
DE2923817C2 (de) *	1979-06-12	1981-07-09	A. Nattermann & Cie GmbH, 5000 Köln	(3-Alkylamino-2-hydroxyproposy)-furan-2-carbonsäureanilide und deren physiologisch verträgliche Säureadditionssalze und Verfahren zu deren Herstellung sowie Arzneimittel mit einem Gehalt dieser Verbindungen
US4914097A (en) *	1987-02-25	1990-04-03	Mitsubishi Kasei Corporation	N-indanyl carboxamide derivative and agricultural/horticultural fungicide containing the derivative as active ingredient
DE4237986A1 (de) *	1992-11-11	1994-05-19	Bayer Ag	Verwendung von Furancarboxamiden im Materialschutz
US5977168A (en)	1994-04-15	1999-11-02	Sankyo Company, Limited	Wood preservative compositions containing dimethylfurancarboxyanilide derivatives
GB9424379D0 (en) *	1994-12-02	1995-01-18	Agrevo Uk Ltd	Fungicides
EP1275301A1 (en) *	2001-07-10	2003-01-15	Bayer CropScience S.A.	Trisubstituted heterocyclic compounds and their use as fungicides
DE10222884A1 (de) *	2002-05-23	2003-12-04	Bayer Cropscience Ag	Furancarboxamide
EP1548007A1 (en)	2003-12-19	2005-06-29	Bayer CropScience S.A.	2-Pyridinylethylcarboxamide derivatives and their use as fungicides
EP1879878B1 (en) *	2005-04-08	2014-06-25	Bayer CropScience AG	Heterocyclylethylheterocyclylcarboxamide derivatives as fungicides
AU2010353001B2 (en)	2010-05-12	2015-01-15	Sds Biotech K. K.	Preservative for preserving wood and method for treating wood
US11589583B2 (en)	2013-12-03	2023-02-28	Fmc Corporation	Pyrrolidinones herbicides
BR112017020094B1 (pt)	2015-04-27	2022-01-11	Fmc Corporation	Composto, composições herbicidas, mistura de herbicida e método para controlar o crescimento de vegetação indesejada
EP3650430A1 (en)	2015-05-12	2020-05-13	FMC Corporation	Intermediates and processes for the synthesis of herbicides
EP3303287B1 (en)	2015-05-29	2020-12-16	FMC Corporation	Substituted cyclic amides as herbicides
RU2017142979A (ru)	2015-06-02	2019-07-15	ЭфЭмСи Корпорейшн	Замещенные циклические амиды и их применение в качестве гербицидов
RU2720994C2 (ru)	2015-07-31	2020-05-15	Е.И.Дюпон Де Немур Энд Компани	Новые соединения циклического n-карбоксамида, применяемые в качестве гербицидов
BR112019012910B1 (pt)	2016-12-21	2023-10-17	Fmc Corporation	Composto, composição herbicida, mistura herbicida e método para controlar o crescimento de vegetação indesejável
KR20240006708A (ko)	2017-03-21	2024-01-15	에프엠씨 코포레이션	피롤리디논 및 이의 제조 방법
WO2018175231A1 (en)	2017-03-21	2018-09-27	Fmc Corporation	Herbicidal mixture, composition and method
AR111967A1 (es)	2017-05-30	2019-09-04	Fmc Corp	Amidas herbicidas
AR111839A1 (es)	2017-05-30	2019-08-21	Fmc Corp	Lactamas 3-sustituidas herbicidas
TWI743976B (zh) *	2020-09-04	2021-10-21	國立中興大學	有害生物防治組合物

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Publication number	Priority date	Publication date	Assignee	Title
US2166118A (en) *	1936-10-03	1939-07-18	Du Pont	Insecticidal compositions containing heterocyclic amides
US3152136A (en) *	1958-10-30	1964-10-06	Dow Chemical Co	Dinitroaroyl-nu-pyridyl amides
US3354157A (en) *	1961-06-02	1967-11-21	Hooker Chemical Corp	Trichlorofuramides
GB1052507A (tr) *	1963-06-26
GB1215066A (en) *	1968-03-25	1970-12-09	Shell Int Research	Acrylamides and their use as fungicides
DE1768686B1 (de) *	1968-06-19	1971-05-27	Basf Ag	Furan-3-carbonsaeureanilide und deren Verwendung als Fungizid
CA932334A (en) *	1969-02-13	1973-08-21	Kulka Marshall	Furan-3-carboxamide derivatives and method of preparing same

1969
- 1969-02-13 US US04/799,110 patent/US3959481A/en not_active Expired - Lifetime
1970
- 1970-02-09 GB GB608470A patent/GB1302410A/en not_active Expired
- 1970-02-09 ZA ZA700862A patent/ZA70862B/xx unknown
- 1970-02-10 NO NO00466/70A patent/NO129602B/no unknown
- 1970-02-10 IL IL33881A patent/IL33881A/xx unknown
- 1970-02-11 SE SE7001750A patent/SE395590B/xx unknown
- 1970-02-12 NL NLAANVRAGE7002031,A patent/NL171957B/xx not_active Application Discontinuation
- 1970-02-12 PL PL1970138769A patent/PL82624B1/pl unknown
- 1970-02-12 BE BE745864D patent/BE745864A/xx not_active IP Right Cessation
- 1970-02-12 DE DE2006471A patent/DE2006471C2/de not_active Expired
- 1970-02-12 CS CS70992A patent/CS188868B2/cs unknown
- 1970-02-12 FR FR7005055A patent/FR2033330B1/fr not_active Expired
- 1970-02-12 DK DK68770AA patent/DK134232B/da not_active Application Discontinuation
- 1970-02-13 JP JP45012043A patent/JPS5010376B1/ja active Pending
- 1970-02-13 TR TR18587A patent/TR18587A/tr unknown
- 1970-02-13 BR BR216721/70A patent/BR7016721D0/pt unknown
- 1970-02-13 LU LU60344D patent/LU60344A1/xx unknown
- 1970-02-13 AT AT133770A patent/AT300460B/de not_active IP Right Cessation
- 1970-02-13 CH CH211470A patent/CH557141A/xx not_active IP Right Cessation
- 1970-02-13 ES ES376540A patent/ES376540A1/es not_active Expired
- 1970-02-13 SU SU1404699A patent/SU433664A3/ru active

Also Published As

Publication number	Publication date
LU60344A1 (tr)	1971-06-21
AT300460B (de)	1972-07-25
NL171957B (nl)	1983-01-17
NL7002031A (tr)	1970-08-17
FR2033330B1 (tr)	1974-05-03
FR2033330A1 (tr)	1970-12-04
IL33881A (en)	1984-09-30
DE2006471A1 (de)	1970-08-27
DK134232B (da)	1976-10-04
PL82624B1 (tr)	1975-10-31
BR7016721D0 (pt)	1973-05-31
CS188868B2 (en)	1979-03-30
JPS5010376B1 (tr)	1975-04-21
ES376540A1 (es)	1972-06-16
SE395590B (sv)	1977-08-22
DE2006471C2 (de)	1988-07-28
US3959481A (en)	1976-05-25
GB1302410A (tr)	1973-01-10
BE745864A (fr)	1970-08-12
IL33881A0 (en)	1970-04-20
CH557141A (de)	1974-12-31
ZA70862B (en)	1971-09-29
TR18587A (tr)	1977-04-13
SU433664A3 (ru)	1974-06-25

Publication	Publication Date	Title
NO129602B (tr)	1974-05-06
PL97786B1 (pl)	1978-03-30	Srodek szkodnikobojczy i regulujacy wzrost roslin
HU222444B1 (hu)	2003-07-28	Tiofénkarboxamid-származék és alkalmazása növények torzsgomba betegségének kezelésére
JPS60260505A (ja)	1985-12-23	農園芸用殺菌剤
SU518105A3 (ru)	1976-06-15	Фунгицид
RU1834637C (ru)	1993-08-15	Способ борьбы с грибками
WO2015135422A1 (zh)	2015-09-17	一种保护植物免于植物病害的方法
PL144333B1 (en)	1988-05-31	Fungicide
DK167876B1 (da)	1993-12-27	Fremgangsmaade til bekaempelse af afgroedeangribende svampe, fungicidt middel til anvendelse ved udoevelse af fremgangsmaaden samt aminophosphonsyreforbindelser
CN107517981A (zh)	2017-12-29	一种农药组合物及其应用
JPH02264770A (ja)	1990-10-29	植物を病気から保護するための組成物
BG64312B1 (bg)	2004-09-30	Производно на тиадиазол карбоксамид, средство за контролиране на болести по растенията и методи за неговото използване
JPS63284162A (ja)	1988-11-21	ヒドラジン誘導体、その組成物及び微生物に対する植物保護方法
JPS6368505A (ja)	1988-03-28	農業用殺虫殺菌組成物
DK145495B (da)	1982-11-29	Fungicidt virksomt 1-substitueret-benzimidazol-2-carbaminsyremethylester til anvendelse ved plantebeskyttelse
CN101322492A (zh)	2008-12-17	一种防治水稻恶苗病和立枯病的农药
JPH04504266A (ja)	1992-07-30	殺菌性３―イミノ―１，４―オキサチイン
Singh et al.	2012	Grain yield loss in mungbean due to web blight
JPH0248572A (ja)	1990-02-19	新規なチアゾール化合物及びその製造方法並びに該化合物を有効成分とする殺菌剤組成物
CZ299799B6 (cs)	2008-11-26	Zpusob prípravy 4,5-dimethyl-N-2-propenyl-2-(trimethylsilyl)-3-thiofenkarboxamidu; 4-hydroxy-4,5-dimethyl-N-2-propenyl-2-(trimethylsilyl)-3-thiofenkarboxamid, jeho použití pro výrobu fungicidu a fungicidní kompozice, které jej obsahují
NO124777B (tr)	1972-06-05
US3879553A (en)	1975-04-22	Control of rice blast with 4-halo-carbostyrils and -isocarbostyrils
CN109776545A (zh)	2019-05-21	一种***并嘧啶抗菌剂及其农药组合物
JPH1025210A (ja)	1998-01-27	殺菌性ピラゾール類
WO2018162449A1 (en)	2018-09-13	Use of beta-cyclocitric acid or a salt thereof to enhance plant tolerance to drought stress