SU298095A1 - - Google Patents

Info

Publication number

SU298095A1

SU298095A1 SU1278406A SU1278406A SU298095A1 SU 298095 A1 SU298095 A1 SU 298095A1 SU 1278406 A SU1278406 A SU 1278406A SU 1278406 A SU1278406 A SU 1278406A SU 298095 A1 SU298095 A1 SU 298095A1

Authority

SU

USSR - Soviet Union

Prior art keywords

compounds

integer

pesticide

case

plants

Prior art date

Links

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• 239000000575 pesticide Substances 0.000 description 8
• 150000001875 compounds Chemical class 0.000 description 7
• 125000000217 alkyl group Chemical group 0.000 description 5
• 241000196324 Embryophyta Species 0.000 description 4
• 241000238631 Hexapoda Species 0.000 description 4
• -1 cyclopropanecarboxylic acid ester Chemical class 0.000 description 3
• 229910052736 halogen Inorganic materials 0.000 description 3
• 150000002367 halogens Chemical class 0.000 description 3
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
• 241001454293 Tetranychus urticae Species 0.000 description 2
• 239000013543 active substance Substances 0.000 description 2
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
• 239000000460 chlorine Substances 0.000 description 2
• 229910052801 chlorine Inorganic materials 0.000 description 2
• 125000000753 cycloalkyl group Chemical group 0.000 description 2
• 125000004663 dialkyl amino group Chemical group 0.000 description 2
• 235000013601 eggs Nutrition 0.000 description 2
• 239000000839 emulsion Substances 0.000 description 2
• 125000001188 haloalkyl group Chemical group 0.000 description 2
• 229910052739 hydrogen Inorganic materials 0.000 description 2
• 239000001257 hydrogen Substances 0.000 description 2
• 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
• 229910052760 oxygen Inorganic materials 0.000 description 2
• 239000001301 oxygen Substances 0.000 description 2
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
• 238000002360 preparation method Methods 0.000 description 2
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
• 125000001424 substituent group Chemical group 0.000 description 2
• 229910052717 sulfur Inorganic materials 0.000 description 2
• 239000011593 sulfur Substances 0.000 description 2
• 241000219122 Cucurbita Species 0.000 description 1
• 241000122098 Ephestia kuehniella Species 0.000 description 1
• IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
• 241001465754 Metazoa Species 0.000 description 1
• 241000488583 Panonychus ulmi Species 0.000 description 1
• 241000219833 Phaseolus Species 0.000 description 1
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
• 241000607479 Yersinia pestis Species 0.000 description 1
• 239000004480 active ingredient Substances 0.000 description 1
• 239000007864 aqueous solution Substances 0.000 description 1
• 239000011324 bead Substances 0.000 description 1
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
• 239000012141 concentrate Substances 0.000 description 1
• 239000007859 condensation product Substances 0.000 description 1
• YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical class OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 description 1
• CWIHITONTXITGT-UHFFFAOYSA-L disodium;1-benzyl-2-heptadecyl-3h-benzimidazole-2,4-disulfonate Chemical compound [Na+].[Na+].CCCCCCCCCCCCCCCCCC1(S([O-])(=O)=O)NC(C(=CC=C2)S([O-])(=O)=O)=C2N1CC1=CC=CC=C1 CWIHITONTXITGT-UHFFFAOYSA-L 0.000 description 1
• 239000002270 dispersing agent Substances 0.000 description 1
• 230000001999 effect on insects Effects 0.000 description 1
• 230000000694 effects Effects 0.000 description 1
• 230000002538 fungal effect Effects 0.000 description 1
• 125000001475 halogen functional group Chemical group 0.000 description 1
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
• 231100000053 low toxicity Toxicity 0.000 description 1
• 238000000034 method Methods 0.000 description 1
• 150000002894 organic compounds Chemical class 0.000 description 1
• 239000000546 pharmaceutical excipient Substances 0.000 description 1
• 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
• 150000003014 phosphoric acid esters Chemical class 0.000 description 1
• 239000000843 powder Substances 0.000 description 1
• 239000000243 solution Substances 0.000 description 1
• 239000007921 spray Substances 0.000 description 1
• 239000004563 wettable powder Substances 0.000 description 1
• 238000009736 wetting Methods 0.000 description 1
• 239000000080 wetting agent Substances 0.000 description 1