Abstract:
NOVEL SPIRO BENZOCYCLANE ACETIC ACID COMPOUNDS OF THE FORMULA
(-(CH2)2-Y-(CH2)2-)>C 1,2-PHENYLENE)-)
WHEREIN R IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN AND LINEAR AND BRANCHED ALKLY OF 1 TO 4 CARBON ATOMS. R1 IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, CHLORINE, TRIFLUOROMETHYL AND LOWER ALKOXY, Y IS SELECTED FROM THE GROUP CONSISTING OF METHYLENE, OXYGEN AND SULFUR, N IS 2, 3 OR 4 AND R2 IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN SUBSTITUTED OR UNSUBSTITUTED ALKYL OF 1 TO 6 CARBON ATOMS AND CATION OF NON-TOXIC, PHARMACEUTICALLY ACCEPTABLE MINERAL AND ORGANIC BASES, PROCESSES FOR THEIR PREPRATION AND NOVEL INTERMEDIATES. THE COMPOUNDS OF FORMULA I HAVE ANALGESIC AND ANTI-INFLAMMATORY PROPERTIES.
Abstract:
An organophosphate ester having the formula
WHEREIN A represents a divalent radical selected from the group consisting of alkylene having three to five carbon atoms, aza substitued alkylene having three to five carbon atoms in the chain and thia substituted alkylene having three to five carbon atoms in the chain, Y'' represents a member selected from the group consisting of hydrogen, alkyl having one to six carbon atoms, cyano, halo and alkylthio having one to six carbon atoms, X represents a member selected from the group consisting of sulfur and oxygen, R1'''' represents an alkyl having one to four carbon atoms, R2'''' represents a member selected from the group consisting of alkyl having one to four carbon atoms, alkoxy having one to four carbon atoms, alkoxyalkoxy having one to four carbon atoms in each alk, and
WHERE R1'' and R2'' are members selected from the group consisting of hydrogen and alkyl having one to three carbon atoms; as well as the process of producing said organophosphate esters. The compounds have insecticidal and acaricidal properties.
Abstract:
NOVEL SPRIO BENZOCYCLANE ACETIC ACID COMPOUND OF THE FORMULA WHEREIN R IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN AND LINEAR AND BRANCHED ALKYL OF 1 TO 4 CARBON ATOMS R1 IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, CHLORINE, TRIFLUOROMETHYL AND LOWER ALKOXY, Y IS SELECTED FROM THE GROUP CONSISTING OF METHYLENE, OXYGEN AND SULFUR, N IS 2,3, OR 4 AND R2 IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, SUBSTITUTED OR UNSUBSTITUTED ALKYL OF 1 TO 6 CARBON ATOMS AND CATION OF NONTOXIC, PHARMACEUTICALLY ACCEPTABLE MINERAL AND ORGANIC BASES. PROCESSES FOR THEIR PREPARATION AND NOVEL INTERMEDIATES. THE COMPOUNDS OF FORMULA 1 HAVE ANALGESIC AND ANTI-INFLAMMATORY PROPERTIES.
Abstract:
DIALKYLSULFOXIMINOCARBONYLMETHYL THIOPHOSPHATES HAVING THE FORMULA
R1-O-P(=X)(-O-R2)-S-CH2-CO-N=S(=O)(-R3)-R4
WHEREIN R1, R2, R3 AND R4 ARE ALKYL HAVING FROM 1 TO 7 CARBON ATOMS AND X REPRESENTS A MEMBER SELECTED FROM THE GROUP CONSISTING OF OXYGEN AND SULFUR; THE PROCESS OF MANUFACTURE, PESTICIDAL COMPOSITIONS AND THE ACARICIDAL METHOD. THE SAID THIOPHOSPHATES POSSESS ACARICIDAL PROPERTIES.