SU334659A1 - - Google Patents

Info

Publication number

SU334659A1

SU334659A1 SU1418141A SU1418141A SU334659A1 SU 334659 A1 SU334659 A1 SU 334659A1 SU 1418141 A SU1418141 A SU 1418141A SU 1418141 A SU1418141 A SU 1418141A SU 334659 A1 SU334659 A1 SU 334659A1

Authority

SU

USSR - Soviet Union

Prior art keywords

dicyano

nitroaniline

compounds

alkyl

plants

Prior art date

Links

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• 241000196324 Embryophyta Species 0.000 description 11
• 150000001875 compounds Chemical class 0.000 description 8
• 239000004009 herbicide Substances 0.000 description 7
• 125000000217 alkyl group Chemical group 0.000 description 6
• 125000003342 alkenyl group Chemical group 0.000 description 4
• 230000002363 herbicidal effect Effects 0.000 description 4
• 239000001257 hydrogen Substances 0.000 description 4
• 229910052739 hydrogen Inorganic materials 0.000 description 4
• 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
• -1 M-Cyclohexyl Chemical group 0.000 description 3
• 230000000694 effects Effects 0.000 description 3
• LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Substances [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 3
• UZJZIZFCQFZDHP-UHFFFAOYSA-N 3-nitrobenzene-1,2-dicarbonitrile Chemical class [O-][N+](=O)C1=CC=CC(C#N)=C1C#N UZJZIZFCQFZDHP-UHFFFAOYSA-N 0.000 description 2
• QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
• 125000004183 alkoxy alkyl group Chemical group 0.000 description 2
• 150000001412 amines Chemical class 0.000 description 2
• 125000003710 aryl alkyl group Chemical group 0.000 description 2
• 125000003118 aryl group Chemical group 0.000 description 2
• 125000000753 cycloalkyl group Chemical group 0.000 description 2
• 230000006378 damage Effects 0.000 description 2
• 229910052757 nitrogen Inorganic materials 0.000 description 2
• 125000004433 nitrogen atom Chemical group N* 0.000 description 2
• BKJAXBDANXXYKI-UHFFFAOYSA-N 2-methoxy-3,5-dinitrobenzonitrile Chemical compound COC1=C(C#N)C=C([N+]([O-])=O)C=C1[N+]([O-])=O BKJAXBDANXXYKI-UHFFFAOYSA-N 0.000 description 1
• UMEXFFROBIZXRZ-UHFFFAOYSA-N 4-chloro-5-nitrobenzene-1,3-dicarbonitrile Chemical compound ClC1=C(C=C(C=C1[N+](=O)[O-])C#N)C#N UMEXFFROBIZXRZ-UHFFFAOYSA-N 0.000 description 1
• FEHMHLXCTFGDPA-UHFFFAOYSA-N C(#N)C1=C(C(=C(C=C1)OC)[N+](=O)[O-])C#N Chemical compound C(#N)C1=C(C(=C(C=C1)OC)[N+](=O)[O-])C#N FEHMHLXCTFGDPA-UHFFFAOYSA-N 0.000 description 1
• 229920000742 Cotton Polymers 0.000 description 1
• XFJAHMMKMPKKBN-UHFFFAOYSA-N N-(4-cyanophenyl)-N-nitronitramide Chemical class C(#N)C1=CC=C(N([N+](=O)[O-])[N+](=O)[O-])C=C1 XFJAHMMKMPKKBN-UHFFFAOYSA-N 0.000 description 1
• 240000008042 Zea mays Species 0.000 description 1
• 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
• 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
• 150000001298 alcohols Chemical class 0.000 description 1
• 229910021529 ammonia Inorganic materials 0.000 description 1
• 150000001555 benzenes Chemical class 0.000 description 1
• 235000013339 cereals Nutrition 0.000 description 1
• 239000013043 chemical agent Substances 0.000 description 1
• 229940125904 compound 1 Drugs 0.000 description 1
• 239000000839 emulsion Substances 0.000 description 1
• 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
• 230000003993 interaction Effects 0.000 description 1
• 235000009973 maize Nutrition 0.000 description 1
• 238000000034 method Methods 0.000 description 1
• 125000005429 oxyalkyl group Chemical group 0.000 description 1
• 239000006072 paste Substances 0.000 description 1
• 230000008832 photodamage Effects 0.000 description 1
• 239000000843 powder Substances 0.000 description 1
• 239000002689 soil Substances 0.000 description 1
• 239000000243 solution Substances 0.000 description 1
• 239000000725 suspension Substances 0.000 description 1