SU289538A1 - - Google Patents

Info

Publication number

SU289538A1

SU289538A1 SU1230798A SU1230798A SU289538A1 SU 289538 A1 SU289538 A1 SU 289538A1 SU 1230798 A SU1230798 A SU 1230798A SU 1230798 A SU1230798 A SU 1230798A SU 289538 A1 SU289538 A1 SU 289538A1

Authority

SU

USSR - Soviet Union

Prior art keywords

disease

plants

control plants

trichloromethylthiophthalimide

fungicide

Prior art date

Links

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• Global Dossier
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• 201000010099 disease Diseases 0.000 description 5
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 5
• 230000000855 fungicidal effect Effects 0.000 description 3
• 239000000126 substance Substances 0.000 description 3
• CDIJOYCNNFLOAX-UHFFFAOYSA-N 4-(trichloromethylsulfanyl)isoindole-1,3-dione Chemical class ClC(Cl)(Cl)SC1=CC=CC2=C1C(=O)NC2=O CDIJOYCNNFLOAX-UHFFFAOYSA-N 0.000 description 2
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
• 239000013543 active substance Substances 0.000 description 2
• 239000000417 fungicide Substances 0.000 description 2
• XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical class C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 2
• 230000000975 bioactive effect Effects 0.000 description 1
• 150000001875 compounds Chemical class 0.000 description 1
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
• 239000003814 drug Substances 0.000 description 1
• 229940079593 drug Drugs 0.000 description 1
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
• 229910052736 halogen Inorganic materials 0.000 description 1
• 125000005843 halogen group Chemical group 0.000 description 1
• 238000011081 inoculation Methods 0.000 description 1
• 239000007788 liquid Substances 0.000 description 1
• 238000000034 method Methods 0.000 description 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
• -1 methyl mercapto group Chemical group 0.000 description 1
• 244000052769 pathogen Species 0.000 description 1
• 230000001717 pathogenic effect Effects 0.000 description 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
• 230000010152 pollination Effects 0.000 description 1
• 230000001681 protective effect Effects 0.000 description 1
• 239000007921 spray Substances 0.000 description 1
• 235000013547 stew Nutrition 0.000 description 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
• 239000012224 working solution Substances 0.000 description 1