Claims
- 1. A chemical compound selected from the group consisting of an imidazole derivative having the formula ##STR50## and the active acid addition salts thereof wherein Ar is a member selected from the group consisting of phenyl, mono-, di- and trihalophenyl, methylphenyl, ethylphenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl and trihalomethylphenyl, and R is a member selected from the group consisting of (C.sub.1 -C.sub.10) alkyl, cycloalkyl, alkenyl, cycloalkenyl and aralkyl, said aryl being a member selected from the group consisting of phenyl, mono-, di- and trihalophenyl, methylphenyl, ethylphenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl and trihalomethylphenyl, provided that when Ar is unsubstituted phenyl then R is (C.sub.4 -C.sub.10) alkyl, cycloalkyl, alkenyl, cycloalkenyl and arylalkyl, said aryl being a member selected from the group consisting of phenyl, mono-, di- and trihalophenyl, methylphenyl, ethylphenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl and trihalomethylphenyl,
- 2. A chemical compound selected from the group consisting of an imidazole derivative having the formula ##STR51## and the active acid addition salts thereof wherein Ar is a member selected from the group consisting of phenyl, mono-, di- and trihalophenyl, methylphenyl, ethylphenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl and trihalomethylphenyl, and R is a member selected from the group consisting of alkenyl, cycloalkenyl and aralkyl, said aryl being a member selected from the group consisting of phenyl, mono-, di- and trihalophenyl, methylphenyl, ethylphenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl and trihalomethylphenyl.
- 3. A chemical compound selected from the group consisting of an imidazole having the formula ##STR52## and the active acid addition salts thereof wherein Ar is a member selected from the group consisting of phenyl, mono-, di- and trihalophenyl, methylphenyl, ethylphenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl and trihalomethylphenyl, and R is a member selected from the group consisting of (C.sub.1 -C.sub.10) alkyl and cycloalkyl provided that when Ar is unsubstituted phenyl then R is (C.sub.4 -C.sub.10) alkyl or cycloalkyl.
- 4. A chemical compound selected from the group consisting of 1-[2-(2,4-dichlorophenyl)hexyl]-1H-imidazole and the active acid addition salts thereof.
- 5. A chemical compound selected from the group consisting of 1-[2-(2,4-dichlorophenyl)decyl]-1H-imidazole and the active acid addition salts thereof.
- 6. A chemical compound selected from the group consisting of 1-[2-(2,4-dichlorophenyl)-4-methylpentyl]-1H-imidazole and the active acid addition salts thereof.
- 7. A chemical compound selected from the group consisting of an imidazole derivative having the formula ##STR53## and the active acid addition salts thereof wherein Ar is a member selected from the group consisting of phenyl, mono-, di- and trihalophenyl, methylphenyl, ethylphenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl and trihalomethylphenyl, and R is a member selected from the group consisting of (C.sub.1 -C.sub.10) alkyl, (C.sub.3 -C.sub.7) cycloalkyl, (C.sub.2 -C.sub.12) alkenyl, (C.sub.5 -C.sub.7) cycloalkenyl and (C.sub.7 -C.sub.9) arylalkyl, said aryl being a member selected from the group consisting of phenyl, mono-, di- and trihalophenyl, methylphenyl, ethylphenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl and trihalomethylphenyl.
- 8. A chemical compound according to claim 7 wherein R is (C.sub.4 -C.sub.10) alkyl, (C.sub.3 -C.sub.7) cycloalkyl, (C.sub.2 -C.sub.12) alkenyl, (C.sub.5 -C.sub.7) cycloalkenyl and (C.sub.7 -C.sub.9) arylalkyl, said aryl being a member selected from the group consisting of phenyl, mono-, di-, and trihalophenyl, methylphenyl, ethylphenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl and trihalomethylphenyl when Ar is unsubstituted phenyl.
- 9. A chemical compound according to claim 7 wherein R is a member selected from the group consisting of (C.sub.1 -C.sub.10) alkyl and (C.sub.3 -C.sub.7) cycloalkyl provided that when Ar is unsubstituted phenyl then R is (C.sub.4 -C.sub.10) alkyl or (C.sub.3 -C.sub.7) cycloalkyl.
- 10. A method for controlling phytopathogenic fungi which comprises applying to a plant, to plant seeds or to the plant habitat an effective amount of a compound of the formula: ##STR54## and the active acid addition salts thereof wherein Ar is a member selected from the group consisting of phenyl, mono-, di- and trihalophenyl, methylphenyl, ethylphenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl and trihalomethylphenyl, and R is a member selected from the group consisting of (C.sub.1 -C.sub.10) alkyl, (C.sub.3 -C.sub.7) cycloalkyl, (C.sub.2 -C.sub.12) alkenyl, (C.sub.5 -C.sub.7) cycloalkenyl and (C.sub.7 -C.sub.9) aralkyl, said aryl being a member selected from the group consisting of phenyl, mono-, di- and trihalophenyl, methylphenyl, ethylphenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl and trihalomethylphenyl.
- 11. A method according to claim 10 wherein the compound is applied to the plant or plant habitat at a rate of 0.1 to 50 lbs. per acre.
- 12. A method according to claim 10 wherein the compound is applied to the plant seeds at a rate of 0.1 to 20 ounces per hundred pounds of seed.
- 13. A fungicidal composition for controlling phytopathogenic fungi which comprises an agronomically acceptable carrier and, as the active ingredient, a compound of the formula: ##STR55## and the active acid addition salts thereof wherein Ar is a member selected from the group consisting of phenyl, mono-, di- and trihalophenyl, methylphenyl, ethylphenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl and trihalomethylphenyl, and R is a member selected from the group consisting of (C.sub.1 -C.sub.10) alkyl, (C.sub.3 -C.sub.7) cycloalkyl, (C.sub.2 -C.sub.12) alkenyl, (C.sub.5 -C.sub.7) cycloalkenyl and (C.sub.7 -C.sub.9) aralkyl, said aryl being a member selected from the group consisting of phenyl, mono-, di- and trihalophenyl, methylphenyl, ethylphenyl, methoxyphenyl, ethoxyphenyl, nitrophenyl and trihalomethylphenyl.
SUMMARY OF THE INVENTION
This application is a continuation-in-part application of United States application Ser. No. 642,041, filed Dec. 8, 1975, now U.S. Pat. No. 4,105,762 which is a continuation-in-part application of United States application Ser. No. 547,291, filed Feb. 5, 1975, now abandoned.
US Referenced Citations (10)
Foreign Referenced Citations (2)
Number |
Date |
Country |
1487326 |
May 1967 |
FRX |
6751M |
Apr 1969 |
FRX |
Non-Patent Literature Citations (2)
Entry |
Cannon et al., J. Org. Chem., 1957, vol. 22, pp. 1323-1326. |
Lespagnol et al., J. Chim. Ther., 1966, vol. 66, pp. 292-300. |
Continuation in Parts (2)
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Number |
Date |
Country |
Parent |
642041 |
Dec 1975 |
|
Parent |
547291 |
Feb 1975 |
|