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US4123556A Expired / Lapsed US ⏱️ 0.0 years remaining

Insecticidal composition

Assignee: Novartis Corp
•
Filing: 1975-09-18
•
Granted: 1978-10-31
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Expires: 1995-09-18
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Abstract

Abstract Compounds of the formula ##STR1## wherein R 1 represents hydrogen, halogen, C 1 -C 4 -alkyl, vinyl or ethynyl, R 2 represents hydrogen, halogen, methyl or ethyl, or R 1 and R 2 together represent the cyclopentyl or cyclohexy ring, R 3 represents hydrogen, halogen, methyl, ethyl or C 1 -C 4 -alkoxy, R 4 represents hydrogen, halogen or methyl, R 5 represents hydrogen or halogen, or R 3 and R 5 together represent a carbon-carbon-bond, or an oxygen bridge, R 6 represents hydrogen, methyl or ethyl, R 7 represents cyclohexyl or the group ##STR2## R 8 represents hydrogen, halogen, C 1 -C 4 -alkyl or C 1 -C 4 -alkoxy, Y represents oxygen or the group ##STR3## whereby the ##STR4## group is bound to the phenyl ring, Z represents hydrogen or methyl, and m and n each represent the number 0 or 1 A method for their manufacture and their use for the control of insects and members of the order acarina are disclosed.

Inventors

  • 👤 Friedrich Karrer

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 19:26
CPC Classifications
C; C07; C07D; C07D303/00; C07D303/02; C07D303/12; C07D303/18; C07D303/20; C07D303/24; C07C; C07C43/00; C07C43/02; C07C43/257; C07C43/263; Y; Y10; Y10S; Y10S424/00; Y10S424/12

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 175 words
A method for combatting insects by inhibiting the development of the larvae, or pupae, thereof which comprises treating, by contact or ingestion, an immature form of said insect with a development inhibiting amount of a compound of the formula ##STR76## wherein R 1 represents hydrogen, halogen, C 1 -C 4 -alkyl, vinyl or ethynyl, R 2 represents hydrogen, halogen, methyl or ethyl, or R 1 and R 2 together represent the cyclopentyl or cyclohexyl ring, R 3 represents hydrogen, halogen, methyl, ethyl or C 1 -C 4 -alkoxy, R 4 represents hydrogen, halogen or methyl, R 5 represents hydrogen or halogen, or R 3 and R 5 together represent a carbon-carbon bond, R 6 represents hydrogen, methyl or ethyl, R 7 represents cyclohexyl or the group ##STR77## R 8 represents hydrogen, halogen, C 1 -C 4 -alkyl or C 1 -C 4 -alkoxy, Y represents oxygen, or the group ##STR78## whereby the ##STR79## is bound to the phenyl ring, Z represents hydrogn or methyl, and m and n each represent the number 0 to 1.
Claim 2
Independent Claim 175 words
A method for combatting insects by inhibiting the development of the larvae, or pupae, thereof which comprises treating, by contact or ingestion, an immature form of said insect with a development inhibiting amount of a compound of the formula ##STR76## wherein R 1 represents hydrogen, halogen, C 1 -C 4 -alkyl, vinyl or ethynyl, R 2 represents hydrogen, halogen, methyl or ethyl, or R 1 and R 2 together represent the cyclopentyl or cyclohexyl ring, R 3 represents hydrogen, halogen, methyl, ethyl or C 1 -C 4 -alkoxy, R 4 represents hydrogen, halogen or methyl, R 5 represents hydrogen or halogen, or R 3 and R 5 together represent a carbon-carbon bond, R 6 represents hydrogen, methyl or ethyl, R 7 represents cyclohexyl or the group ##STR77## R 8 represents hydrogen, halogen, C 1 -C 4 -alkyl or C 1 -C 4 -alkoxy, Y represents oxygen, or the group ##STR78## whereby the ##STR79## is bound to the phenyl ring, Z represents hydrogn or methyl, and m and n each represent the number 0 to 1.
Claim 3
Dependent Claim 132 words
The method according to claim 1, wherein in said compound R 1 represents hydrogen, chlorine, methyl, ethyl, n-propyl, isopropyl, n-, i-, sec.-butyl, vinyl or ethynyl, R 2 represents hydrogen, chlorine or methyl, or R 1 and R 2 together represent the cyclopentyl or cyclohexyl ring, R 3 represents hydrogen, emthyl, ethyl, methoxy or ethoxy, R 4 represents hydrogen, chlorine or methyl, R 5 represents hydrogen, or R 3 and R 5 together represent a carbon-carbon bond, R 6 represents hydrogen or methyl, or R 7 represents cyclohexyl, or the group ##STR80## R 8 represents hydrogen, chlorine, methyl, ethyl or ethoxy, Y represents oxygen, or the group ##STR81## whereby the ##STR82## is bound to the phenyl ring, Z represents hydrogen or methyl, and m and n each represent the number 0 or 1.
Claim 4
Dependent Claim 115 words
The method according to claim 2, wherein in said compound R 1 represents hydrogen, chlorine, methyl, ethyl, n-propyl, isopropyl, n-, i-, sec.-butyl, vinyl or ethynyl, R 2 represents hydrogen, chlorine or methyl, R 3 represents hydrogen, methyl, ethyl, methoxy or ethoxy, R 4 represents hydrogen, chlorine or methyl, R 5 represents hydrogen, or R 3 and R 5 together represent a carbon-carbon bond, R 6 represents hydrogen or methyl, R 7 represents the group ##STR83## R 8 represents hydrogen, chlorine, methyl, ethyl or ethoxy, Y represents oxygen, or the group --CH 2 O--, whereby the --CH 2 -- group is bound to the phenyl ring, and m and n represent the number 0 or 1.
Claim 5
Dependent Claim 10 words
The method of claim 3, wherein said compound is 1-phenoxy-4-(4-pentinyl-1-oxy)benzene.
Claim 6
Dependent Claim 10 words
The method of claim 3, wherein said compound is 1-cyclohexyl-oxy-4-(3-methyl-2-pentenyl-1-oxy)-benzene.
Claim 7
Dependent Claim 10 words
The method of claim 3, wherein said compound is 1-phenoxy-4-(3-methyl-3-methoxy-pentyl-1-oxy)-benzene.
Claim 8
Dependent Claim 10 words
The method of claim 3, wherein said compound is 1-phenoxy-4-(3-chloro-2-propenyl-1-oxy)-benzene.
Claim 9
Dependent Claim 10 words
The method of claim 3, wherein said compound is 1-phenoxy-4-(3-methyl-2,4-pentadienyl-1-oxy)-benzene.
Claim 10
Dependent Claim 10 words
The method of claim 3, wherein said compound is 1-phenoxy-4-(4-methyl-3-hexenyl-1-oxy)-benzene.
Claim 11
Dependent Claim 14 words
The method of claim 1 for combatting insects of the order diptera or Coleoptera.

References Cited (Backward Citations)

US3170959A Cited
US3240703A Cited
US3155733A Cited
US3441615A Cited
US3787443A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1981-10-30 1982-05-01 1982-10-31 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1985-10-30 1986-05-01 1986-10-31 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1989-10-30 1990-05-01 1990-10-31 $7700.00 Window Closed / Lapsed

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