1. An auxiliary exhaust structure, for exhausting a pollution source in a workstation, comprising:
an exhaust hood, disposed corresponding to the workstation, having a suction port for sucking the pollution source and a deflector extending along the periphery of the suction port for guiding the pollution source; and
an air feeder, for generating an air flow flowing along the deflector towards the suction port.
2. The auxiliary exhaust structure as claimed in claim 1, wherein the air feeder comprises:
a fan, for generating an air flow; and
an air outlet, disposed at the edge of the deflector to receive and guide the air flow to the deflector.
3. The auxiliary exhaust structure as claimed in claim 2, wherein the air feeder further comprises an air chamber to receive the air flow generated by the fan, regulate the air pressure of the air flow and guide the regulated air flow to the air outlet.
4. The auxiliary exhaust structure as claimed in claim 3, wherein the air chamber is hollow.
5. The auxiliary exhaust structure as claimed in claim 2, wherein the air outlet is provided with a plurality of ribs.
6. The auxiliary exhaust structure as claimed in claim 3, wherein the air chamber surrounds the suction port.
7. The auxiliary exhaust structure as claimed in claim 2, wherein the air outlet is surrounding the edge of the deflector.
8. The auxiliary exhaust structure as claimed in claim 1, wherein the deflector forms an angle with the periphery of the suction port.
9. An auxiliary exhaust structure, for exhausting a pollution source of a workstation, comprising:
an exhaust hood, disposed corresponding to the workstation, having a suction port for sucking the pollution source and a deflector extending along the periphery of the suction port for guiding the pollution source;
an air feeder, for generating an air flow flowing along the deflector towards the suction port; and
an exhauster, disposed at the outer edge of the workstation, for generating an air curtain facing the exhaust hood.
10. The auxiliary exhaust structure as claimed in claim 9, wherein the air feeder comprises:
a fan, for generating the air flow; and
an air outlet, disposed at the edge of the deflector to receive and guide the air flow to the deflector.
11. The auxiliary exhaust structure as claimed in claim 10, wherein the air feeder further comprises an air chamber to receive the air flow generated by the fan, regulate the air pressure of the air flow and guide the regulated air flow to the air outlet.
12. The auxiliary exhaust structure as claimed in claim 11, wherein the air chamber is hollow.
13. The auxiliary exhaust structure as claimed in claim 10, wherein the air outlet is provided with a plurality of ribs.
14. The auxiliary exhaust structure as claimed in claim 11, wherein the air chamber surrounds the suction port.
15. The auxiliary exhaust structure as claimed in claim 10, wherein the air outlet is surrounding the edge of the deflector.
16. The auxiliary exhaust structure as claimed in claim 9, wherein the deflector forms an angles with the periphery of the suction port.
17. The auxiliary exhaust structure as claimed in claim 9, wherein the air curtain faces the suction port.
18. The auxiliary exhaust structure as claimed in claim 9, wherein the air curtain, the workstation, and the exhaust hood together form a surrounding space to surround the pollution source.
19. An auxiliary exhaust method, for exhausting a pollution source of a workstation, comprising:
disposing an exhaust hood corresponding to the workstation, and utilizing a suction port of the exhaust hood to suck the pollution source;
disposing a deflector along the periphery of the suction port; and
disposing an air feeder to generate an air flow flowing along the deflector towards the suction port.
20. The auxiliary exhaust method as claimed in claim 19, wherein before the step of disposing an air feeder to generate an air flow, further comprises a step of disposing an exhauster at the outer edge of the workstation and generating an air curtain from the workstation towards the suction port.
The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.
1. An amide compounds having the general formula I:
Wherein:
R1 and R2 are selected from H, OH, halogen, CN, NO2, C1-C4alkyl, C1-C4haloalkyl, C1-C4alkoxyalkyl, COR11, CO2R11, CONR12R11, C1-C4alkoxy, C1-C4haloalkoxy, NR12R11, NR12COR11, NR12CO2R11, SOmR12, SO2NR12R11, unsubstituted phenyl or substituted phenyl with substituent group(s) being from 1 to 3 in which the substituent group(s) is(are) selected from Cl, Br, F, CN, NO2, C1-C6alkyl, C1-C3haloalkyl, C1-C3haloalkoxy or C1-C3alkoxycarbonyl;
m is selected from 0, 1 or 2;
R3 and R4 are selected from H, C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3-C6cycloalkyl or
C1-C4haloalkyl; or R3 joined together with R1 to form 6-8 membered ring;
X is selected from (CHR5)n; n is integers from 2 to 10; R5 may be the same or different, selected from H, C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3-C6cycloalkyl or C1-C6haloalkyl;
G1 is selected from CR6 or N; G2 is selected from CR7 or N; G3 is selected from CR8 or N; but G1, G2 and G3 can not be N at the same time;
R6, R7 and R8 are selected from H, OH, halogen, CN, NO2, C1-C4alkyl, C3-C6cycloalkyl, CONH2, CONHCH2CN, C1-C3alkoxy, C1-C3haloalkoxy, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3alkoxycarbonyl, C1-C3alkylcarbonyl, C1-C3alkylamino, C2-C6dialkylamino, C3-C6cycloalkylamino, unsubstituted phenyl or substituted phenyl with substituent group(s) being from 1 to 4, unsubstituted phenylamino or substituted phenylamino with substituent group(s) being from 1 to 4, in which the substituent group(s) is(are) selected from Cl, Br, F, CN, NO2, C1-C4alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy or C1-C3alkoxycarbonyl;
R9 is selected from H, OH, halogen, CN, NO2, C1-C4alkyl, C3-C6cycloalkyl, C1-C3haloalkyl, C1-C3alkoxyalkyl, C1-C3alkoxy, C1-C3haloalkoxy, COR11, CO2R11, CONR11R12, NR12R11, NR12COR11, NR12CO2R11, SOmR12, unsubstituted phenyl or substituted phenyl, unsubstituted pyrazolyl or substituted pyrazolyl, unsubstituted pyridyl or substituted pyridyl, in which the substituent group(s) being from 1 to 3 is(are) selected from halogen, CN, NO2, C1-C4alkyl, C3-C6cycloalkyl, C1-C3haloalkyl, C1-C3alkoxyalkyl, C1-C3alkoxy, C1-C3haloalkoxy, COR11, CO2R11, CONR11R12, NR11R12, NR12COR11, NR12CO2R11, SOmR12 or SO2NR11R12;
is selected from 1, 2, 3 or 4;
R10 and R11 are selected from H or C1-C4alkyl;
R12 is selected from H, C1-C4alkyl, C1-C3haloalkyl, unsubstituted phenyl or substituted phenyl, in which the substituent group is selected from Cl, Br, F, CN, NO2, C1-C4alkyl, CF3, OCH3, OCF3 or CO2CH3;
Q is selected from unsubstituted C1-C4alkyl or substituted C1-C4alkyl, unsubstituted cyclopropyl or substituted cyclopropyl, wherein the substituent group(s) being from 1 to 4 is(are) selected from Cl, Br, F or C1-C4alkyl; unsubstituted phenylamino or substituted phenylamino, unsubstituted C2-C4alkenyl or substituted C2-C4alkenyl, in which substituent group(s) being from 1 to 3 is(arc) selected from Cl, Br, F, C1-C4alkyl, C3-C6cycloalkyl, C1-C4haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy or C1-C4alkoxycarbonyl; unsubstituted phenyl or substituted phenyl, unsubstituted pyrazolyl or substituted pyrazolyl, unsubstituted pyridyl or substituted pyridyl, in which substituent group(s) being from 1 to 4 is(are) halogen, CN, NO2, C1-C4alkyl, C3-C6cycloalkyl, C1-C3haloalkyl, C1-C3alkoxyalkyl, C1-C3alkoxy, C1-C3haloalkoxy, COR11, CO2R11, CONR11R12, NR11R12, NR12COR11, NR19CO2R11, SOmR12 or SO2NR11R12.
2. The compounds according to the claim 1, characterized in that wherein general formula I:
R1 is selected from H, OH, Cl, Br, F, NO2, CN, CH3, CH2CH3, tert-butyl, CF3, CH2CF3, OCH3, OCF3, CONH2, CONHCH2CN, CO2CH3 or CO2C2H5;
R2 is selected from H, OH, Cl, Br, F, NO2, CN, CH3, CH2CH3, tert-butyl, cyclopropyl, CF3, CH2CF3, OCF3, OCH2CF3, CO2CH3, CO2C2H5, unsubstituted phenyl or substituted phenyl, in which substituent group(s) being from 1 to 3 is(are) Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, CF3, CH2CF3, OCH3, OCF3, CO2CH3 or CO2C2H5;
R3 and R4 are selected from H or C1-C3alkyl; or R3 joined together with R4 to form six-membered ring;
X is selected from (CHR5)n; n is integers selected from 2 to 10; R5 may be the same or different, selected from H, C1-C3alkyl or C1-C3haloalkyl;
G1 is selected from CR6 or N; G2 is selected from CR7 or N; G3 is selected from CR8 or N; but G1, G2 and G3 can not be N at the same time;
R6, R7 and R8 are selected from H, OH, Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, cyclopropyl, CF3, CH2CF3, OCF3, OCH2CF3, CO2CH3, CONH2, CONHCH7CN, C1-C3alkylamino, C2-C4diallylamino, C3-C6cycloalkylamino, unsubstituted phenyl or substituted phenyl with substituent group(s) being from 1 to 3, unsubstituted phenylamino or substituted phenylamino with substituent group(s) being from 1 to 3, wherein the substituent group(s) is(are) selected from Cl, Br, I, CN, NO2, CH3, CH2CH3, tert-butyl, CHF2, CF3, CH2CF3, OCH3, OCHF2, OCF3, CO2CH3 or CO2C2H5;
R9 is selected from H, Cl, Br, F, CN, NO2, CH3, tert-butyl, CHF2, CF3, OCH3, OCHF2, OCF3, OCH2CF3, SO2CH3, C1-C3alkylamino or C2-C4dialkylamino;
t is selected from 1, 2, 3 or 4;
R10 is selected from H, CH3 or C2H5;
NR10\u2014CO-Q is at the 2, 3 or 4-position of benzene ring;
Q is selected from one of the following groups:
Wherein:
R13 is selected from H, Cl, Br, F, CN, NO2, NH2, CH3, CH2CH3, tert-butyl, cyclopropyl. CF3, CH2CF3, OCH3, OCF3, OCH2CF3, SO2CH3, CO2CH3, C1-C3alkylaminocarbonyl, C2-C4dialkylaminocarbonyl, unsubstituted phenyl or substituted phenyl with substituent group(s) being from 1 to 3, unsubstituted pyridyl or substituted pyridyl with substituent group(s) being from 1 to 3, the substituent group(s) is(are) selected from Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, cyclopropyl, CHF2, CF3, CH2CF3, OCH3, OCHF2, OCF3, OCH2CF3 or SO2CH3;
R14 is selected from H, CH3, CH2CH3, tert-butyl, CF3, CH2CF3, unsubstituted phenyl or substituted phenyl with substituent group(s) being from 1 to 3, unsubstituted pyridyl or substituted pyridyl with substituent group(s) being from 1 to 3, the substituent group(s) is(are) selected from Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, cyclopropyl, CHF2, CF3, CH2CF3, OCHF2, OCF3, OCH2CF3 or SO2CH3;
p is selected from 1 or 2.
3. The compounds according to the claim 2, characterized in that wherein general formula I:
R1 is selected from H, Cl, Br, F, NO2, CN, CH3, CH2CH3, tert-butyl, CF3, CH2CF3, OCH3, OCF3, CO2CH3 or CO2C2H5;
R2 is selected from H, Cl, Br, F, NO2, CN, CH3, CH2CH3, tert-butyl, cyclopropyl, CF3, CH2CF3, OCF3, OCH2CF3, CO2CH3, CO2C2H5, unsubstituted phenyl or substituted phenyl with the substituent group(s) being from 1 to 3 is(are) selected from Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, CF3, CH2CF3, OCH3, OCF3, CO2CH3 or CO2C2H5;
R3 and R4 are selected from H, or C1-C3alkyl; or R3 joined together with R4 to form 6 membered ring;
X is selected from (CHR5),; n is integers selected from 2 to 10; R5 may be the same or different, selected from H, C1-C3alkyl or C1-C3haloalkyl;
G1 is selected from CR6 or N; G2 is selected from CR7 or N; G3 is selected from CR8 or N; but G1, G2 and G3 can not be N at the same time;
R6, R7 and R8 are selected from H, Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, cyclopropyl, CF3, CH2CF3, OCF3, OCH2CF3, CO2CH3, C1-C3alkylamino, C2-C4dialkylamino, cyclopropylamino, unsubstituted phenyl or substituted phenyl with substituent group(s) being from 1 to 3, unsubstituted phenylamino or substituted phenylamino with substituent group(s) being from 1 to 3, the substituent group(s) is(are) selected from Cl, Br, I, CN, NO2, CH3, CH2CH3, tert-butyl, CHF2, CF3, CH2CF3, OCH3, OCHF2, OCF3, CO2CH3 or CO2C2H5;
R9 is selected from H, Cl, Br, F, CN, NO2, CH3, CHF2, CF3, OCH3, OCHF2, OCF3, OCH2CF3 or SO2CH3;
t is selected from 1, 2, 3 or 4;
R10 is selected from H, CH3 or C2H5;
NR10\u2014CO-Q is at the 2, 3 or 4-position of benzene ring;
Q is selected from one of the following groups:
Wherein:
R13 is selected from H, Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, cyclopropyl, CF3, CH2CF3, OCF3, OCH2CF3, SO2CH3, CO2CH3, unsubstituted phenyl or substituted phenyl with substituent group(s) being from 1 to 3, unsubstituted pyridyl or substituted pyridyl with substituent group(s) being from 1 to 3, the substituent group(s) is(are) selected from H, Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, cyclopropyl, CHF2, CF3, CH2CF3, OCH3, OCF3, OCH2CF3 or SO2CH3;
R14 is selected from H, CH3, CH2CH3, tert-butyl, CF3, CH2CF3, unsubstituted phenyl or substituted phenyl with substituent group(s) being from 1 to 3, unsubstituted pyridyl or substituted pyridyl with substituent group(s) being from 1 to 3, the substituent group(s) is(are) selected from Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, cyclopropyl, CHF2, CF3, CH2CF3, OCH3, OCH2, OCF3, OCH2CF3 or SO2CH3;
p is selected from 1 or 2.
4. The compounds according to the claim 3, characterized in that wherein general formula I:
R1 is selected from H, Cl, Br, F, NO2, CN, CH3, tert-butyl, CF3, OCH3 or OCF3;
R\u2014) is selected from H, Cl, Br, F, NO2, CN, CH3, tert-butyl, cyclopropyl, CF3, OCF3, CO2CH3 or CO2C2H5;
R3 and R4 are selected from H or C1-C3alkyl; or R3 joined together with R4 to form 6 membered ring;
X is selected from \u2014CH2CH2\u2014, \u2014CH2CH2CH2\u2014, \u2014CH(CH3)CH2\u2014, \u2014CH(C2H5)CH2\u2014, \u2014CH2(CH2)2CH2\u2014, \u2014CH2(CH2)3CH2\u2014, \u2014CH2(CH2)4CH2\u2014, \u2014CH2(CH2)5CH2\u2014, \u2014CH2(CH2)6CH2\u2014, \u2014CH2(CH2)7CH2\u2014 or \u2014CH2(CH2)8CH2\u2014;
G1 is selected from CR6 or N; G2 is selected from CR7 or N; CH3 is selected from CR8 or N; but G1, G2 and G3 can not be N at the same time;
R6, R7 and R8 are selected from H, Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, cyclopropyl, CF3, CH2CF3, OCF3, OCH2CF3 or CO2CH3;
R9 is selected from H, Cl, Br, F, CN, NO2, CH3, CHF2, CF3, OCH3, OCHF2, OCF3, OCH2CF3 or SO2CH3;
t is selected from 1, 2, 3 or 4;
R10 is selected from H;
NR10\u2014CO-Q is at the 2, 3 or 4-position of benzene ring;
Q is selected from one of the following groups:
Wherein:
R14 is selected from H, CH3, unsubstituted phenyl or substituted phenyl with substituent group(s) being from 1 to 3, unsubstituted pyridyl or substituted pyridyl with substituent group(s) being from 1 to 3, in which the substituent group(s) is(are) selected from Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, CF3, OCH3 or OCF3;
When R14 is selected from H or CH3, R43 is selected from H, Cl, Br, F, CN, CH3, CH2CH3, tert-butyl, cyclopropyl, CF3, OCH3, OCF3, OCH2CF3, SO2CH3, unsubstituted phenyl or substituted phenyl, the substituent group is selected from II. Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, CHF2, CF3, OCH3, OCHF2, OCF3, OCH2CF3 or SO2CH3;
When R14 is selected from (un)substituted phenyl or pyridyl. R13 is selected from Cl, Br, F. CN, CH3, CH2CH3, tert-butyl, cyclopropyl, CF3, OCH3, OCF3, OCH2CF3 or SO2CH3;
p is selected from 1 or 2.
5. The compounds according to the claim 4, characterized in that wherein general formula I:
R1 is selected from H, Cl, Br, F, NO2, CN, CH3 or CF3;
R2 is selected from H, Cl, Br, F, NO2, CN, C1-3, tert-butyl, cyclopropyl, CF3, OCF3, CO2CH3 or CO2C2H5;
R3 and R4 are selected from H, or R3 and R4 in (R3)N\u2014X\u2014N(R1) can join together to form piperazine ring;
X is selected from \u2014CH2CH2\u2014, \u2014CH2CH2CH2\u2014, \u2014CH(CH3)CH2\u2014, \u2014CH(C2H5)CH2\u2014, \u2014CH2(CH2)2CH2\u2014, \u2014CH2(CH2)3CH2\u2014, \u2014CH2(CH2)4CH2\u2014, \u2014CH2(CH2)5CH2\u2014, \u2014CH2(CH2)6CH2\u2014, \u2014CH2(CH2)7CH2\u2014 or \u2014CH2(CH2)6CH2\u2014;
G1 is selected from CR6 or N; G2 is selected from CR7 or N; G3 is selected from CR8 or N; but G1, G2 and G3 can not be N at the same time;
R6, R7 and R8 are selected from H, Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, cyclopropyl, CF3, OCH3 or CO2CH3;
R9 is selected from H, Cl, Br, F, CN, NO2, CH3, CHF2, CF3, OCH3, OCHF2, OCF3, OCH2CF3 or SO2CH3;
t is selected from 1 or 2;
R10 is selected from 11;
NR10\u2014CO-Q is at the 2 or 4-position of benzene ring;
Q is selected from the following pyrazolyl groups:
Wherein:
R14 is selected from H, CH3, unsubstituted phenyl or substituted phenyl with substituent group(s) being from 1 to 3, unsubstituted pyridyl or substituted pyridyl both with substituent group(s) being from 1 to 3, the substituent group(s) is(are) selected from Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, CF3, OCH3 or OCF3;
When R14 is selected from H or CH3, R43 is selected from H, Cl, Br, F, CN, CH3, CH2CH3, tert-butyl, CF3, OCH3, OCF3, SO2CH3, unsubstituted phenyl or substituted phenyl with substituent group, the substituent group is selected from H, Cl, Br, F, CN, NO2, CH3, CH2CH3, tert-butyl, CHF2, CF3, OCH3, OCHF2, OCF3 or SO2CH3;
When R14 is selected from (un)substituted phenyl or pyridyl. R13 is selected from H, Cl, Br, F. CN, CH3, CH2CH3, tert-butyl, CF3, OCH3, OCF3 or SO2CH3;
p is selected from 1 or 2.
6. A process for preparing the compounds having general formula I according to claim 1, which comprises reacting an amine group compound having general formula IV with substituted benzoxazinone having general formula V-A or aromatic acid chloride having general formula V-B in the presence of base:
Wherein:
L is leaving group, selected from Cl or Br;
R1 and R2 are selected from H, OH, halogen, CN, NO2, C1-C4alkyl, C1-C4haloalkyl, C1-C4alkoxyalkyl, COR11, CO2R11, CONR12R11, C1-C4alkoxy, C1-C4haloalkoxy, NR12R11, NR12COR11, NR12CO2R11, SOmR12, SO2NR12R11, unsubstituted phenyl or substituted phenyl, in which the substituent group is selected from Cl, Br, F, CN, NO2, C1-C3haloalkyl, C1-C3haloalkoxy or C1-C3alkoxycarbonyl;
m is selected from 0, 1 or 2;
R3 and R4 are selected from H, C1-C6alkyl C2-C6alkenyl, C2-C6alkynyl, C3-C6cycloalkyl or C1-C4haloalkyl; or R3 joined together with R4 to form 6-8 membered ring;
X is selected from (CHR5)n; n is integers selected from 2 to 10; R5 may be the same or different, selected from H, C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3-C6cycloalkyl or C1-C6haloalkyl;
G1 is selected from CR6 or N; G2 is selected from CR7 or N; G3 is selected from CR8 or N; but G1, G2 and G3 can not be N at the same time;
R6, R7 and R8 are selected from H, OH, halogen, CN, NO2, C1-C4alkyl, C3-C6cycloalkyl, CONH2, CONHCH7CN, C1-C3alkoxy, C1-C3haloalkoxy, C1-C3alkylthio, C1-C3alkylsulfinyl, C1-C3alkylsulfonyl, C1-C3alkoxycarbonyl, C1-C3alkylcarbonyl, C1-C3alkylamino, C2-C6dialkylamino, C3-C6cycloalkylamino, unsubstituted phenyl or substituted phenyl with substituent group(s) being from 1 to 4, unsubstituted phenylamino or substituted phenylamino with substituent group(s) being from 1 to 4, the substituent group(s) is(are) selected from Cl, Br, F, CN, NO2, C1-C4alkyl, C1-C3haloalkyl, C1-C3alkoxy, C1-C3haloalkoxy or C1-C3alkoxycarbonyl;
R9 is selected from H, OH, halogen, CN, NO2, C1-C4alkyl, C3-C6cycloalkyl, C1-C3haloalkyl, C1-C3alkoxyalkyl, C1-C3alkoxy, C1-C3haloalkoxy, COR11, CO2R11, CONR11R12, NR12R11, NR12COR11, NR12CO2R11, SOn, R12, SO2NR12R11, unsubstituted phenyl or substituted phenyl with substituent group(s) being from 1 to 3, unsubstituted pyrazolyl or substituted pyrazolyl with substituent group(s) being from 1 to 3, unsubstituted pyridyl or substituted pyridyl with substituent group(s) being from 1 to 3, in which the substituent group(s) is(are) selected from halogen, CN, NO2, C1-C4alkyl, C3-C6cycloalkyl, C1-C3haloalkyl, C1-C3alkoxyalkyl, C1-C3alkoxy, C1-C3haloalkoxy, COR11, CO2R11, CONR11R12, NR11R12, NR12COR11, NR12CO2R11, SOmR12 or SOmNR11R12;
t is selected from 1, 2, 3 or 4;
R10 and R11 are selected from H or C1-C4alkyl;
R12 is selected from H, C1-C4alkyl C1-C3haloalkyl, unsubstituted phenyl or substituted phenyl, in which the substituent group is selected from Cl, Br, F, CN, NOD, C1-C4alkyl, CF3, OCH3, OCF3 or CO2CH3;
Q is selected from unsubstituted C1-C4alkyl or substituted C1-C4alkyl with substituent group(s) being from 1 to 4, unsubstituted cyclopropyl or substituted cyclopropyl with substituent group(s) being from 1 to 4, in which the substituent group(s) is(are) selected from Cl, Br, F or C1-C4alkyl; unsubstituted phenylamino or substituted phenylamino with substituent group(s) being from 1 to 3, unsubstituted C1-C4alkenyl or substituted C1-C4alkenyl with substituent group(s) being from 1 to 3, in which the substituent group(s) is(are) selected from Cl, Br, F, C1-C4alkyl, C3-C6cycloalkyl, C1-C4haloalkyl, C1-C4alkoxy, C1-C4haloalkoxy or C1-C4alkoxycarbonyl; unsubstituted phenyl or substituted phenyl with substituent group(s) being from 1 to 3, unsubstituted pyrazolyl or substituted pyrazolyl with substituent group(s) being from 1 to 3, unsubstituted pyridyl or substituted pyridyl with substituent group(s) being from 1 to 3, in which the substituent group(s) is(arc) selected from halogen, CN, NOD, C1-C4alkyl C3-C6cycloalkyl, C1-C3haloalkyl, C1-C3alkoxyalkyl, C1-C3alkoxy, C1-C3haloalkoxy, COR1E, CO2R11, CONR11R12, NR11R12, NR12COR11, NR12CO2R11, SOmR12 or SO2NR11R12.
7. A method of controlling fungi which comprises applying the compound having general formula I according to claim 1 to agricultural and other fields.
8. A method of controlling insects which comprises applying the compound having general formula I according to claim 1 to agricultural and other fields.
9. An insecticidal or fungicidal composition comprising the compound having general formula I according to the claim 1 as an active ingredient, wherein the weight percentage of the active ingredient in the composition is in the range of 0.1-99%.