RU99110738A - FUNGICIDE MIXTURES - Google Patents
FUNGICIDE MIXTURESInfo
- Publication number
- RU99110738A RU99110738A RU99110738/04A RU99110738A RU99110738A RU 99110738 A RU99110738 A RU 99110738A RU 99110738/04 A RU99110738/04 A RU 99110738/04A RU 99110738 A RU99110738 A RU 99110738A RU 99110738 A RU99110738 A RU 99110738A
- Authority
- RU
- Russia
- Prior art keywords
- locus
- pyridylaniline
- formula
- derivative
- acrylic acid
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims 8
- 230000000855 fungicidal Effects 0.000 title claims 5
- 239000000417 fungicide Substances 0.000 title 1
- HUDSSSKDWYXKGP-UHFFFAOYSA-N N-phenylpyridin-2-amine Chemical class C=1C=CC=NC=1NC1=CC=CC=C1 HUDSSSKDWYXKGP-UHFFFAOYSA-N 0.000 claims 7
- QNBTYORWCCMPQP-JXAWBTAJSA-N (Z)-dimethomorph Chemical compound C1=C(OC)C(OC)=CC=C1C(\C=1C=CC(Cl)=CC=1)=C/C(=O)N1CCOCC1 QNBTYORWCCMPQP-JXAWBTAJSA-N 0.000 claims 4
- XLPJNCYCZORXHG-UHFFFAOYSA-N 1-morpholin-4-ylprop-2-en-1-one Chemical compound C=CC(=O)N1CCOCC1 XLPJNCYCZORXHG-UHFFFAOYSA-N 0.000 claims 4
- 239000005761 Dimethomorph Substances 0.000 claims 4
- UZCGKGPEKUCDTF-UHFFFAOYSA-N Fluazinam Chemical group [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 claims 4
- 239000005780 Fluazinam Substances 0.000 claims 4
- 125000000547 substituted alkyl group Chemical group 0.000 claims 4
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 3
- 230000002401 inhibitory effect Effects 0.000 claims 3
- 241000233866 Fungi Species 0.000 claims 2
- -1 alkadienyl Chemical group 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 125000004104 aryloxy group Chemical group 0.000 claims 2
- 150000001602 bicycloalkyls Chemical group 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- 125000001072 heteroaryl group Chemical group 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 230000003032 phytopathogenic Effects 0.000 claims 2
- 241000233654 Oomycetes Species 0.000 claims 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
Claims (11)
где R1 и R2 каждый независимо является атомом водорода или галогена или необязательно замещенным алкилом, алкокси, алкенилом, алкинилом, алкадиенилом, арилом, арилокси, гетероарилом, циклоалкилом, циклоалкенилом, бициклоалкилом или гетероциклилом,
(b) и по меньшей мере, одного фунгицидного производного N-пиридиланилина.1. A liquid concentrated fungicidal composition comprising a fungicidally acceptable carrier and / or surface active agent and synergistically effective amounts of (a) at least one acrylic acid morpholide of formula I
where R 1 and R 2 each independently is a hydrogen atom or halogen or an optionally substituted alkyl, alkoxy, alkenyl, alkynyl, alkadienyl, aryl, aryloxy, heteroaryl, cycloalkyl, cycloalkenyl, bicycloalkyl or heterocyclyl,
(b) and at least one fungicidal N-pyridylaniline derivative.
где R3 и R4 каждый независимо представлен атомом водорода или атомом галогена или необязательно замещенной алкильной группой;
Y каждый независимо представлен атомом галогена или необязательно замещенной алкильной группой;
m = 0 или целое число 1, 2, 3 или 4.2. The composition according to claim 1, where the derivative of N-pyridylaniline is a compound of formula II
where R 3 and R 4 each independently represents a hydrogen atom or a halogen atom or an optionally substituted alkyl group;
Y is each independently represented by a halogen atom or an optionally substituted alkyl group;
m = 0 or an integer 1, 2, 3 or 4.
где R1 и R2 каждый независимо является атомом водорода или галогена или необязательно замещенным алкилом, алкокси, алкенилом, алкинилом, алкадиенилом, арилом, арилокси, гетероарилом, циклоалкилом, циклоалкенилом, бициклоалкилом или гетероциклилом,
(b) по крайней мере, одного фунгицидного производного N-пиридиланилина.6. A method of inhibiting the growth of a phytopathogenic fungus in a locus, which includes the use in the locus of synergistically effective amounts (a) of at least one acrylic acid morpholide of formula I
where R 1 and R 2 each independently is a hydrogen atom or halogen or an optionally substituted alkyl, alkoxy, alkenyl, alkynyl, alkadienyl, aryl, aryloxy, heteroaryl, cycloalkyl, cycloalkenyl, bicycloalkyl or heterocyclyl,
(b) at least one fungicidal N-pyridylaniline derivative.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US7802998A | 1998-05-13 | 1998-05-13 | |
US09/078,029 | 1998-05-13 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU99110738A true RU99110738A (en) | 2001-02-27 |
RU2223648C2 RU2223648C2 (en) | 2004-02-20 |
Family
ID=22141479
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU99110738/04A RU2223648C2 (en) | 1998-05-13 | 1999-05-12 | Liquid concentrated fungicide composition and method for inhibition of phytopathogenic fungus growth in locus |
Country Status (12)
Country | Link |
---|---|
EP (1) | EP0956769B1 (en) |
JP (1) | JP4712143B2 (en) |
KR (1) | KR100668179B1 (en) |
AT (1) | ATE244508T1 (en) |
BR (1) | BR9901434B1 (en) |
CA (1) | CA2271820C (en) |
CO (1) | CO5050300A1 (en) |
DE (1) | DE69909365T2 (en) |
IN (1) | IN185139B (en) |
PL (1) | PL194318B1 (en) |
RU (1) | RU2223648C2 (en) |
TR (1) | TR199901040A3 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100424860B1 (en) * | 2000-01-28 | 2004-03-27 | 한국화학연구원 | A absorbtion increasing agent for the foiler uptake of dimethomorph |
CN101617678B (en) * | 2009-07-29 | 2014-07-02 | 深圳诺普信农化股份有限公司 | Pesticide composition |
WO2015068158A1 (en) | 2013-11-07 | 2015-05-14 | Adama Makhteshim Ltd. | Synergistic fungicidal composition |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6052146B2 (en) * | 1979-12-25 | 1985-11-18 | 石原産業株式会社 | N-pyridylaniline compounds, their production methods, and pest control agents containing them |
US5262414A (en) * | 1987-01-30 | 1993-11-16 | Shell Research Limited | Fungicidal compositions |
JP3384882B2 (en) * | 1993-08-11 | 2003-03-10 | 石原産業株式会社 | N-pyridyltoluidine fungicide granular wettable powder |
TW276982B (en) * | 1993-08-11 | 1996-06-01 | Ishihara Sangyo Kaisha | |
EP0806141A1 (en) * | 1996-05-07 | 1997-11-12 | American Cyanamid Company | Enhancement of the efficacy of fungicides |
-
1999
- 1999-05-07 JP JP12721399A patent/JP4712143B2/en not_active Expired - Lifetime
- 1999-05-10 CO CO99028671A patent/CO5050300A1/en unknown
- 1999-05-11 IN IN438CA1999 patent/IN185139B/en unknown
- 1999-05-11 BR BRPI9901434-3A patent/BR9901434B1/en not_active IP Right Cessation
- 1999-05-11 KR KR1019990016773A patent/KR100668179B1/en not_active IP Right Cessation
- 1999-05-11 CA CA002271820A patent/CA2271820C/en not_active Expired - Lifetime
- 1999-05-12 PL PL333088A patent/PL194318B1/en unknown
- 1999-05-12 TR TR1999/01040A patent/TR199901040A3/en unknown
- 1999-05-12 RU RU99110738/04A patent/RU2223648C2/en active
- 1999-05-12 AT AT99303719T patent/ATE244508T1/en not_active IP Right Cessation
- 1999-05-12 DE DE69909365T patent/DE69909365T2/en not_active Expired - Lifetime
- 1999-05-12 EP EP99303719A patent/EP0956769B1/en not_active Expired - Lifetime
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