IT1290855B1 - Composizioni fungicide a base di (n-fenilacetil-n-2,6-xilil)-alaninato di metile - Google Patents
Composizioni fungicide a base di (n-fenilacetil-n-2,6-xilil)-alaninato di metileInfo
- Publication number
- IT1290855B1 IT1290855B1 ITMI962660A IT1290855B1 IT 1290855 B1 IT1290855 B1 IT 1290855B1 IT MI962660 A ITMI962660 A IT MI962660A IT 1290855 B1 IT1290855 B1 IT 1290855B1
- Authority
- IT
- Italy
- Prior art keywords
- alkyl
- methyl
- phenyl
- carbamate
- carbonyl
- Prior art date
Links
- 230000000855 fungicidal effect Effects 0.000 title abstract 3
- 239000000417 fungicide Substances 0.000 title abstract 2
- 230000002195 synergetic effect Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 12
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000002947 alkylene group Chemical group 0.000 abstract 4
- 125000001475 halogen functional group Chemical group 0.000 abstract 4
- -1 6-(2-cyanophenoxy)-pyrimidin-4-yloxy Chemical group 0.000 abstract 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical class [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052802 copper Inorganic materials 0.000 abstract 2
- 239000010949 copper Substances 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 abstract 1
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 abstract 1
- 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 abstract 1
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 abstract 1
- VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 abstract 1
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 abstract 1
- OWDLFBLNMPCXSD-UHFFFAOYSA-N 2-chloro-N-(2,6-dimethylphenyl)-N-(2-oxotetrahydrofuran-3-yl)acetamide Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)C1C(=O)OCC1 OWDLFBLNMPCXSD-UHFFFAOYSA-N 0.000 abstract 1
- QDUDFMMPZWYGFP-UHFFFAOYSA-N 3-anilino-5-methyl-2-methylsulfanyl-5-phenylimidazolidin-4-one Chemical compound CSC1NC(C)(C=2C=CC=CC=2)C(=O)N1NC1=CC=CC=C1 QDUDFMMPZWYGFP-UHFFFAOYSA-N 0.000 abstract 1
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
- 239000005745 Captan Substances 0.000 abstract 1
- 239000005747 Chlorothalonil Substances 0.000 abstract 1
- 239000005756 Cymoxanil Substances 0.000 abstract 1
- 239000005758 Cyprodinil Substances 0.000 abstract 1
- 239000005761 Dimethomorph Substances 0.000 abstract 1
- 239000005764 Dithianon Substances 0.000 abstract 1
- 239000005769 Etridiazole Substances 0.000 abstract 1
- 239000005772 Famoxadone Substances 0.000 abstract 1
- 239000005780 Fluazinam Substances 0.000 abstract 1
- 239000005789 Folpet Substances 0.000 abstract 1
- 239000005790 Fosetyl Substances 0.000 abstract 1
- 239000005805 Mepanipyrim Substances 0.000 abstract 1
- 239000005807 Metalaxyl Substances 0.000 abstract 1
- XFOXDUJCOHBXRC-UHFFFAOYSA-N N-Ethyl-N-methyl-4-(trifluoromethyl)-2-(3,4-dimethoxyphenyl)benzamide Chemical compound CCN(C)C(=O)C1=CC=C(C(F)(F)F)C=C1C1=CC=C(OC)C(OC)=C1 XFOXDUJCOHBXRC-UHFFFAOYSA-N 0.000 abstract 1
- 239000005814 Pencycuron Substances 0.000 abstract 1
- 239000005821 Propamocarb Substances 0.000 abstract 1
- 239000005822 Propiconazole Substances 0.000 abstract 1
- 239000005823 Propineb Substances 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- 239000005840 Tetraconazole Substances 0.000 abstract 1
- 239000005843 Thiram Substances 0.000 abstract 1
- 239000005846 Triadimenol Substances 0.000 abstract 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- IMHBYKMAHXWHRP-UHFFFAOYSA-N anilazine Chemical compound ClC1=CC=CC=C1NC1=NC(Cl)=NC(Cl)=N1 IMHBYKMAHXWHRP-UHFFFAOYSA-N 0.000 abstract 1
- 229940117949 captan Drugs 0.000 abstract 1
- 125000004181 carboxyalkyl group Chemical group 0.000 abstract 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 abstract 1
- 125000002993 cycloalkylene group Chemical group 0.000 abstract 1
- HAORKNGNJCEJBX-UHFFFAOYSA-N cyprodinil Chemical compound N=1C(C)=CC(C2CC2)=NC=1NC1=CC=CC=C1 HAORKNGNJCEJBX-UHFFFAOYSA-N 0.000 abstract 1
- WURGXGVFSMYFCG-UHFFFAOYSA-N dichlofluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=CC=C1 WURGXGVFSMYFCG-UHFFFAOYSA-N 0.000 abstract 1
- WXUZAHCNPWONDH-DYTRJAOYSA-N dimoxystrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1COC1=CC(C)=CC=C1C WXUZAHCNPWONDH-DYTRJAOYSA-N 0.000 abstract 1
- PYZSVQVRHDXQSL-UHFFFAOYSA-N dithianon Chemical compound S1C(C#N)=C(C#N)SC2=C1C(=O)C1=CC=CC=C1C2=O PYZSVQVRHDXQSL-UHFFFAOYSA-N 0.000 abstract 1
- KQTVWCSONPJJPE-UHFFFAOYSA-N etridiazole Chemical compound CCOC1=NC(C(Cl)(Cl)Cl)=NS1 KQTVWCSONPJJPE-UHFFFAOYSA-N 0.000 abstract 1
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [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 abstract 1
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 abstract 1
- VUERQRKTYBIULR-UHFFFAOYSA-N fosetyl Chemical compound CCOP(O)=O VUERQRKTYBIULR-UHFFFAOYSA-N 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- DWKPPFQULDPWHX-VKHMYHEASA-N l-alanyl ester Chemical compound COC(=O)[C@H](C)N DWKPPFQULDPWHX-VKHMYHEASA-N 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- CIFWZNRJIBNXRE-UHFFFAOYSA-N mepanipyrim Chemical compound CC#CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 CIFWZNRJIBNXRE-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- HIIRDDUVRXCDBN-OBGWFSINSA-N metominostrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1OC1=CC=CC=C1 HIIRDDUVRXCDBN-OBGWFSINSA-N 0.000 abstract 1
- YQYKFSVTESXLFN-UHFFFAOYSA-N o-methyl 1,2,3-benzothiadiazole-7-carbothioate Chemical compound COC(=S)C1=CC=CC2=C1SN=N2 YQYKFSVTESXLFN-UHFFFAOYSA-N 0.000 abstract 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 abstract 1
- OGYFATSSENRIKG-UHFFFAOYSA-N pencycuron Chemical compound C1=CC(Cl)=CC=C1CN(C(=O)NC=1C=CC=CC=1)C1CCCC1 OGYFATSSENRIKG-UHFFFAOYSA-N 0.000 abstract 1
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 abstract 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 abstract 1
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000003003 spiro group Chemical group 0.000 abstract 1
- 125000005031 thiocyano group Chemical group S(C#N)* 0.000 abstract 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 abstract 1
- 229960002447 thiram Drugs 0.000 abstract 1
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 abstract 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
Priority Applications (21)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT96MI002660 IT1290855B1 (it) | 1996-12-19 | 1996-12-19 | Composizioni fungicide a base di (n-fenilacetil-n-2,6-xilil)-alaninato di metile |
| BRPI9714423-1A BR9714423B1 (pt) | 1996-12-19 | 1997-12-06 | composições pesticidas com base em alaninato de (n-fenilacetil-n-2,6-xilil) metil |
| ES01203103T ES2190425T3 (es) | 1996-12-19 | 1997-12-06 | Procedimiento para la preparacion de alaninato de (n-fenilacetil-n-2,6-xilil)metilo. |
| ES97953792T ES2182147T3 (es) | 1996-12-19 | 1997-12-06 | Composiciones fungicidas basadas en alaninato de (n-fenilacetil-n-2,6-xilil)metilo. |
| DE69718835T DE69718835T2 (de) | 1996-12-19 | 1997-12-06 | Verfahren zur Herstellung von (N-Phenylacetyl-N-2,6-xylyl)methyl Alaninat |
| PCT/EP1997/006968 WO1998026654A2 (en) | 1996-12-19 | 1997-12-06 | Fungicidal compositions based on (n-phenylacetyl-n-2,6-xylyl)methyl alaninate |
| EP01203103A EP1155616B1 (en) | 1996-12-19 | 1997-12-06 | Process for the preparation of (N-phenylacetyl-N-2,6-xylil)methyl alaninate |
| CU1999077A CU22888A3 (es) | 1996-12-19 | 1997-12-06 | Composiciones fungicidas basadas en alaninato de (n-fenilacetil-n-2,6-xilil)metilo. |
| HU0000480A HU227487B1 (en) | 1996-12-19 | 1997-12-06 | Fungicidal compositions based on (n-phenylacetyl-n-2,6-xylyl)methyl alaninate (benalaxyl), use thereof |
| US09/331,168 US6228885B1 (en) | 1996-12-19 | 1997-12-06 | Fungicidal compositions based on (N-phenylacetyl-N-2,6-XYLYL)methyl alaninate |
| PL97334184A PL189827B1 (pl) | 1996-12-19 | 1997-12-06 | Kompozycje grzybobójcze |
| DE69715038T DE69715038T2 (de) | 1996-12-19 | 1997-12-06 | Auf (n-phenylacetyl-n-2,6-xylyl)methylalaninat basierte fungizide zusammensetzungen |
| AU57567/98A AU5756798A (en) | 1996-12-19 | 1997-12-06 | Fungicidal compositions based on (n-phenylacetyl-n-2,6-xylyl)methyl alaninate |
| IL130534A IL130534A (en) | 1996-12-19 | 1997-12-06 | Fungicidal compositions based on (n - phenylacetyl- n - 2,6 - xylyl) methyl alaninate |
| CNB971814295A CN1225972C (zh) | 1996-12-19 | 1997-12-06 | 基于(n－苯乙酰基－n－2,6－二甲苯基)氨基丙酸甲酯的杀真菌组合物 |
| PT97953792T PT946093E (pt) | 1996-12-19 | 1997-12-06 | Composicoes fungicidas baseadas em alaninato de (n-fenilacetil-n-2,6-xili)metilo |
| EP97953792A EP0946093B1 (en) | 1996-12-19 | 1997-12-06 | Fungicidal compositions based on (n-phenylacetyl-n-2,6-xylyl)methyl alaninate |
| OA9900132A OA11130A (en) | 1996-12-19 | 1999-06-18 | Fungicidal compositions based on (N-phenylacetyl-N-2,6-xylyl)methal alaninate |
| HK00103734A HK1024385A1 (en) | 1996-12-19 | 2000-06-21 | Fungicidal compositions based on (n-phenylacetyl-n-2,6-xylyl)methyl alaninate |
| HK02103821.7A HK1043710B (zh) | 1996-12-19 | 2002-05-21 | (n-苯乙酰-n-2，6-二甲苯基)甲基丙氨酸的製備方法 |
| HUS1100025C HUS1100025I1 (hu) | 1996-12-19 | 2011-12-02 | N-(fenil-acetil)-N-(2,6-xilil)-metil-alaninát(benalaxil) alapú szinergetikus fungicid készítmények és alkalmazásuk |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT96MI002660 IT1290855B1 (it) | 1996-12-19 | 1996-12-19 | Composizioni fungicide a base di (n-fenilacetil-n-2,6-xilil)-alaninato di metile |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| ITMI962660A0 ITMI962660A0 (it) | 1996-12-19 |
| ITMI962660A1 ITMI962660A1 (it) | 1998-06-19 |
| IT1290855B1 true IT1290855B1 (it) | 1998-12-14 |
Family
ID=11375426
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IT96MI002660 IT1290855B1 (it) | 1996-12-19 | 1996-12-19 | Composizioni fungicide a base di (n-fenilacetil-n-2,6-xilil)-alaninato di metile |
Country Status (1)
| Country | Link |
|---|---|
| IT (1) | IT1290855B1 (it) |
-
1996
- 1996-12-19 IT IT96MI002660 patent/IT1290855B1/it active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| ITMI962660A1 (it) | 1998-06-19 |
| ITMI962660A0 (it) | 1996-12-19 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 0001 | Granted |