Use of substituted 2-thiazolines as nitrification inhibitors
AssigneeBASF SE
InventorsPeter Nesvadba, Allan F. Cunningham, Shrirang Hindalekar, Barbara Nave, Tejas Pothi, Alexander Wissemeier
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Abstract
The invention relates to novel nitrification inhibitors of formula I, which are substituted 2-thiazoline compounds. Moreover, the invention relates to the use of compounds of formula I as nitrification inhibitors, i.e. for reducing nitrification, as well as agrochemical mixtures and compositions comprising the nitrification inhibitors of formula I.
Claims18
A substituted 2-thiazoline compound of formula I
- or a salt, stereoisomer, tautomer, N-oxide, or S-oxide thereof for use as a nitrification inhibitor,
- wherein
- R1, R2, R3 and R4 are independently of each other selected from H, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C2-C6-alkenyl, C3-C6-cycloalkyl, C1-C4-alkylsulfonyl, benzyl, hetaryl, and phenyl, wherein said groups are unsubstituted or substituted by one or more, same or different substituents Rx;
- or
- R1 and R2 or R3 and R4 together form ═O, or ═CRC1RC2, wherein RC1 and RC2 together form a 5- or 6-membered saturated, partially or fully unsaturated, or aromatic carbocyclic or heterocyclic ring, wherein said heterocyclic ring comprises one or more, same or different heteroatoms selected from O, N or S, wherein said N- and/or S-atoms are independently oxidized or non-oxidized, and wherein each substitutable carbon or heteroatom in the aforementioned cyclic moieties is independently unsubstituted or substituted with one or more, same or different substituents Rx;
- and wherein
- RS is H, C1-C2-alkyl, C3-C6-cycloalkyl, allyl, propargyl, or phenyl, wherein said groups are unsubstituted or substituted by one or more, same or different substituents Ry;
- CHRaC(═O)ORb, CHRaC(═O)O−Q+, CHRaC(═O)Rd, CHRaC(═O)NRbRc, C(═O)Rd, C(═O)ORb, C(═O)NRbRc, CHRaORb, C(═O)(CH2)2C(═O)ORb, or CSNRbRc;
- Ra is H, halogen, C1-C6-alkyl, C1-C6-alkoxy, C1-C4-haloalkyl, C3-C6-cycloalkyl, phenyl, or phenyl-C1-C2-alkyl;
- Rb is H, C1-C6-alkyl, C1-C6-alkoxy, C3-C6-cycloalkyl, aryl, phenyl, or phenyl-C1-C2-alkyl;
- Rc is H, C1-C6-alkyl, C1-C6-alkoxy, C3-C6-cycloalkyl, aryl, phenyl, or phenyl-C1-C2-alkyl;
- Rd is H, C1-C6-alkyl, C1-C6-haloalkyl, C2-C6-alkenyl, C2-C6-alkynyl, phenyl, phenyl-C1-C2-alkyl, hetaryl, or hetaryl-C2-C3-alkenyl, wherein these groups are unsubstituted or substituted by one or more, same or different substituents selected from halogen, OH, OCH3, and CH3;
- Rx is halogen, OH, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy, C1-C6-alkylthio, C1-C6-alkylcarbonyl, or C1-C6-alkylcarboxy;
- Ry is halogen, OH, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, or C1-C6-haloalkoxy;
- and
- Q+ is selected from the group consisting of Na+, K+, Ca2+, and NH4+.
A substituted 2-thiazoline compound of formula I
- wherein the compound of formula I is selected from
The method of claim 10, wherein said compound of formula I is used in combination with a fertilizer.
The method of claim 10, wherein said reduction of nitrification occurs in or on a plant, in the root zone of a plant, in or on soil or soil substituents and/or at the locus where a plant is growing or is intended to grow.
Dependencies are inferred from the claim text.