ApplicationNo. 05/483882 filed on 06/27/1974
US Classes:558/3, Oxygen attached directly to the nitrogen of the thioimidate group by nonionic bonding (i.e., HO-N=CH-S-, wherein substitution may be hydrogen only)552/12, Having -C(=X)-, wherein X is chalcogen, attached indirectly to the azide group by acyclic nonionic bonding558/301, Oxygen bonded directly to the double bonded nitrogen (e.g., alpha-oximino nitriles, etc.)558/391, Carbon, also in the chain, double bonded to the nitrogen558/437, The sulfur is double bonded to oxygen558/438, Two carbons bonded directly to the same divalent sulfur558/439, Additional cyano group558/441, Oxygen bonded directly to the carbonyl group (e.g., carboxylic acid esters, etc.)558/442, Additional carbonyl attached indirectly to the cyano group by nonionic bonding558/444, The oxygen is between the carbonyl and the cyano group (e.g., cyano is in the alcohol portion of a carboxylic acid ester, etc.)558/7, Oxygen attached directly to the nitrogen of the imidate group by nonionic bonding (i.e., HO-N=CH-O-, wherein substitution may be made for hydrogen only)560/13, Plural nitrogens in acid moiety560/153, Nitrogen or halogen in acid moiety560/16, Nitrogen in acid moiety560/251, Plural nitrogens in alcohol moiety564/102Sulfur attached directly to amino nitrogen by nonionic bonding (e.g., sulfenamides, etc.)
ExaminersPrimary: Brust, Joseph Paul
Attorney, Agent or Firm
AbstractNovel N-haloalkanesulfenylcarbamoyloxime compositions have been found to have exceptional miticidal and insecticidal activity.