U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

2-benzoyl pyrrole and benzoyl imidazole herbicides

Patent 5512537 Issued on April 30, 1996. Estimated Expiration Date: Icon_subject March 2, 2014. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

3644631

Pyrrolyl oxyphenyl ketones
Patent #: 4000160
Issued on: 12/28/1976
Inventor: Bailey

Preparation of ଲ-acyl pyrroles
Patent #: 4002643
Issued on: 01/11/1977
Inventor: Carson

Fungicides
Patent #: 4863503
Issued on: 09/05/1989
Inventor: Anthony ,   et al.

Heterocyclic compounds as fungicides Patent #: 5091407
Issued on: 02/25/1992
Inventor: deFraine, et al.

Inventor

Assignee

Application

No. 205213 filed on 03/02/1994

US Classes:

504/287, Having -C(=X)-, wherein X is chalcogen, bonded directly to the five-membered hetero ring501/123Alkaline earth metal compound containing

Examiners

Primary: Robinson, Allen J.
Assistant: Bembenick, Brian G.

Attorney, Agent or Firm

Foreign Patent References

  • 337277 EP. 10/13/1989
  • 2198726 GB. 06/13/1988

International Class

A01N 043/36

Abstract

Herbicidal compounds have the formula ##STR1## in which R1 is hydrogen, methyl, ethyl, phenyl, 2-methylphenyl, 3-trifluoromethylphenyl, benzyl, 2-methylbenzyl or vinyl;R2 is hydrogen, methyl, ethyl or chloro;R3 is C1 -C4 alkyl, C1 -C4 alkoxy, C1 -C4 haloalkyl, nitro, p-tolyloxy or p-chlorophenoxy;R4 is hydrogen or a methyl, methoxy, trifluoromethoxy or halo group at the 2, 4- or 5-position;m is --CH or N; andX is O or NOR5 in which R5 is methyl or ethyl; provided that:(a) when R1 is methyl, and(i) R3 is methyl, then R4 is 4-methyl, 4-methoxy or chloro;(ii) R3 is nitro, then R4 is methoxy;(b) when R1 is ethyl, R3 is methyl or methoxy;(c) when R2 is chloro, R3 and R4 are independently C1 -C4 haloalkyl, C1 -C4 haloalkoxy or C1 -C4 alkoxy;(d) when R2 is methyl or ethyl, R1 is hydrogen;(e) when R3 is hydrogen, R4 is 2-methyl, halo or methoxy;(f) if M is N, R3 is C1 -C4 alkoxy, C1 -C4 haloalkyl or C1 -C4 haloalkoxy and R1 is not ethyl; and(g) if R1 is vinyl, M is N.

Other References

  • T. Ohmori et al., "Production of Pyoluteorin and Its Derivatives from n-Paraffin by Pseudomonas aeruginosa S10B2", Agric. Biol. Chem., 42(11), 2031-2036, 197
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