180483. lajstromszámú szabadalom • [Pirimidil-oxi(vagy- tio)]-fenoxi- (vagy-tio)-alkánkarbonsav származékokat tartalmazó herbicid készítmények és eljárás a hatóanyagok előállítására

5 180 483 6 Vegyü­let száma A B D E X Y R1 R* G 12. H H H H O o —ch3 H —OC2H5 13. H —Cl H H o o —ch3 H —oc2h5 14. H —Cl H H o o —ch3 H —och3 15. H —Br H H 0 o —ch3 H —och3 16. H —I H H 0 0 —ch3 H —oc2h5 17. —ch3 h —CHa H o 0 —CH3 H —co2h6 18. —CH3 —Br —ch3 H 0 0 —ch3 H —oc2h5 19. H —Br H 3—t — —Bu o 0 —ch3 H —oc2h6 20. —CH3 —Br H H o o —ch3 H —oc2h6 21. H —Ph H H o o —ch3 H —oc2H5 22. H —CN H H 0 0 —ch3 H —oc2h6 23. H —COOC2Hs H H o o _€H3 H —och3 24. H —Br H H o 0 —CHS —CH 3 —OC2H5 25. H —Br H H o 0-CsH5 H —oc2h5 26. H —Br H H 0 0 n—C6H13 H-oc2h5 27. H —Cl H H 0 o —ch3 —CH , —OC2H6 2.8. H —Br H H o o —ch3 H —O—n—C4Ha 29. H — CH3 H H o 0 —ch3 H —oc2h5 30. H —CH3 H H o 0 —ch3 H —OH 31. —COOCjHu —Cl H H o o —ch3 H —OC2H6 32. —OCH3 —Br H H 0 0 —ch3 H —och3 33. H —Br H 3—Cl 0 0 —ch3 H —oc2h6 34. H —Br H 2—CT 0 o —ch3 H —och3 35. H —Br H 2—Cl 0 o —ch3 H —oc2h6 36. H —Br H H o 0 —ch3 H —och2ch=ch2 37. H —I H H 0 o —ch3 H —och3 38. H —Br H H 0 o —ch3 H —och2c=ch 39. H 4—Cl—C„H4 H H o o —ch3 H —och3 40. H 4—N02—C6H4 H H o 0 —ch3 H —OCH, 41. H —Br H H 0 0 —CH, H-N(C2H5)2 42. H —Cl H H s 0 —CH, H —oc2h5 43. H —Br H H o o —CH, H —OC(CCl,)(CH,)a 44. H —Cl H 3—CT o o —CH, H —OCH, 45. H —Cl H 2—N02 0 0 —CHa H —oc2h6 46. H —Cl H H o s —CHa H —OCH, 47. H —Cl H 2—Cl 0 0 —CH„ H —OCH, 48. H —Cl H 3—C1 0 0 —CHa H —OCH, 49. H —F H H 0 0 —CH, H —OCH, 50. H —I H 2—C1 o 0 —CH, H —OCH, 51. H .. —Cl H 2—Cl o o —CH. H —OH 52. H —OC2H5 H H o 0 —CH, H —OH 53. H —Cl H 2—CF, 0 0 —CHa H —OC2H6 54. H —Br H H 0 o —CH, H 2-tienil-metil-amino-. 55. H —Br H H 0 o —CH, H morfolino-56. H —Br H H o 0 —CH, H fenilamino-57. H —Br H H o 0 —CH, H p-nitro-fenoxi-58. H —Br H H o 0 —CH, H —O—CH2—CeH5 59. H —Br H H o o —CH, H —SCHa—CH = CH2 60. H —Br H H o o —CH, H —sch2c6h5 61. —Cl H H H o 0 —CH, H —OCH, 62. H —Br H H o 0 —CH, H —OH 63. H —Br H H 0 0 —CH, H —O—n—C,H, 64. H —Br H H o 0 —CH, H —OCH(CH,)a 65. H —Br H H o o —CH, H —OCH2CH(CH,)2 66. H —Br H H 0 o —CH, H —OCH(CH,)—C2H5 67. H —Br H H 0 o —CH, H —OC6Hu(n) 68. H —Br H H o o —CH, H —OCH(CH,)— CH2CH(CH,)2 69. H —Br H H o o —CH, H ciklohexil-oxi-3

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