Dow Agrosciences LLC

Jaime Susanne Nugent

David Anthony Demeter

Ricky Hunter

Annette Vitale Brown

Gary D Crouse

Thomas Clarence Sparks

William Hunter Dent, Iii

Kristy Bryan

CaSandra Lee McLeod

Jack Geno Samaritoni

Denise Perreault Cudworth

Carla Nanette Yerkes

Yuanming Zhu

Christian Thomas Lowe

Brent Jeffrey Rieder

William Kirkland Brewster

Chenglin Yao

Noormohamed Mohamed Niyaz

Thomas L Siddall

Katherine Anne Guenthenspberger

Carla J R Klittich

W Randal Erickson

Terry William Balko

William Randal Erickson

Carla Jean Rasmussen Klittich

Casandra Mcleod

William Dent

Annette Brown

Jack Samaritoni

The invention disclosed in this document is related to the field of pesticides and their use in controlling pests. A compound having the following structure is disclosed. 

Pesticidal compositions

The present disclosure relates to 1- or 2-(4-(aryloxy)-phenyl)ethylamino-oxy- or sulfanyl) pteridines and 1- or 2-(4 Jheteroaryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and their use as agrochemicals and animal health products. The disclosure provides compounds of Formula (I-A) and Formula (I-B). 

Compositions comprising substituted pteridines as agrochemicals

The present disclosure relates to 1- or 2-(4-(aryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and 1- or 2-(4-(heteroaryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and their use as agrochemicals and animal health products. More specifically, the invention provides new compounds of the formula (I-A): wherein: R is H, CH, phenyl, or a heterocycle comprising a 5 or 6 membered single ring or a fused ring system comprising at least one 5 or 6 membered heterocycle optionally substituted with H, halo, lower alkyl, lower alkoxy, benzyloxy, lower alkenyl, lower alkynyl, haloalkyl, haloalkoxy, NO, CN, lower alkoxycarbonyl, lower alkylcarbonyl, lower alkyl-SO, and aldoximes and lower alkyloximes, optionally substituted on oxygen by lower alkyl. Z is H, a C&#x2014;C single bond, CH, NH, O, S, CN, CHO, OCH, CHCHO, or OCHCH: m is 4; p is 0 or 1; q is an integer from 0 to 2; Ris independently H, halo, lower alkyl, lower alkenyl, lower alkynyl, hydroxy, lower alkoxy, haloalkyl, haloalkoxy, NO, CN, lower alkylcarbonyl, lower alkoxycarbonyl, mercapto, lower alkylthio, aldoximes and lower alkyloximes, optionally substituted on oxygen by lower alkyl; Y is a C&#x2014;C single bond, C(R)O or C(R); n is 2.

Pteridines and their use as agrochemicals

(1,3,5)-Triazinyl phenyl hydrazones are effective at controlling insects.

Insecticidal (1,3,5)-triazinyl phenyl hydrazones

The present invention relates to thieno[2,3-d]-pyrimidine compounds having fungicidal activity. Specifically, the present invention relates to compounds having the Formula (I): wherein each R1, R2 and R3 is independently selected from the group consisting of H, halogen, and alkyl; A is selected from the group consisting of H and alkyl; W is selected from the group consisting of NH and O; D is selected from O, NH and S; E is (&#x2014;C(O)&#x2014;)&#x2014;R', wherein p is 0 or 1 and R&#x2032; is selected from the group consisting of optionally substituted rings selected from phenyl. furanyl, pyridinyl, pyridinyl-N-oxide, pyrimidinyl, pyridazinyl, pyrazinyl, thiazolyl, triazinyl, thiadiazolyl, oxazolyl, isoxazolyl, thienopyrimidinyl, and pyrimidine fused with an aromatic or heteroaromatic ring selected from bejizene, oxazole, isoxazole, furan, thiazole, pyrimidine, pyridine, pyrrole, pyrazine, and thionhene; each ring being ontionally substituted with one or more substituents selected from the group consisting of alkyl, alkenyl, alkynyl, halogen, haloalkyl, alkoxy, haloalkoxy, nitro, cyano, alkylsulfonyl, alkylsulfoxide, alkylthio, alkoxyiminoalkyl, alkylcarbonyl, alkoxycarbonyl, aminocarbonyl, hydroxycarbonyl, phenyicarbonyl, forrnyl, hydrazidocarbonyl, amidoamino, pyrazolyl, triazolonyl, oxadiazolyl, phenyl, nyridinyl, and phenoxyalkyl; B is selected from the group consisting of halogen, alkyl, haloalkyl, and haloalkoxy; n is an integer from 0 to 3; and m is an integer from 0 to 4 with the proviso that when D is O or S and E is phenyl, then E is not further substituted with halogen.

Thieno-pyrimidine compounds having fungicidal activity

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Brownsburg, IN, United States of America

Jaime Susanne Nugent