JP2010524985A5 - - Google Patents

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Publication number

JP2010524985A5

JP2010524985A5 JP2010504503A JP2010504503A JP2010524985A5 JP 2010524985 A5 JP2010524985 A5 JP 2010524985A5 JP 2010504503 A JP2010504503 A JP 2010504503A JP 2010504503 A JP2010504503 A JP 2010504503A JP 2010524985 A5 JP2010524985 A5 JP 2010524985A5

Authority

JP

Japan

Prior art keywords

alkyl

unsubstituted

substituted

alkoxy

haloalkoxy

Prior art date

2008-04-16

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Granted

Links

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• 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 45
• 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 7
• 125000000217 alkyl group Chemical group 0.000 claims description 5
• -1 carbonyl halide Chemical class 0.000 claims description 2
• 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 42
• 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 42
• 229910052736 halogen Inorganic materials 0.000 claims 40
• 150000002367 halogens Chemical class 0.000 claims 40
• 229910052739 hydrogen Inorganic materials 0.000 claims 37
• 239000001257 hydrogen Substances 0.000 claims 30
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 29
• 150000001875 compounds Chemical class 0.000 claims 27
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 22
• 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 19
• 125000004093 cyano group Chemical group *C#N 0.000 claims 16
• 125000000623 heterocyclic group Chemical group 0.000 claims 15
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 14
• 229920006395 saturated elastomer Polymers 0.000 claims 14
• 150000003839 salts Chemical class 0.000 claims 13
• 125000004414 alkyl thio group Chemical group 0.000 claims 9
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 9
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 8
• 238000000034 method Methods 0.000 claims 8
• 125000004433 nitrogen atom Chemical group N* 0.000 claims 8
• 229910052757 nitrogen Inorganic materials 0.000 claims 7
• 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims 6
• 125000002837 carbocyclic group Chemical group 0.000 claims 6
• 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 5
• 239000003905 agrochemical Substances 0.000 claims 5
• 244000038559 crop plants Species 0.000 claims 5
• 239000000203 mixture Substances 0.000 claims 5
• 238000009472 formulation Methods 0.000 claims 3
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
• 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims 2
• 239000003795 chemical substances by application Substances 0.000 claims 2
• 230000000694 effects Effects 0.000 claims 2
• 239000004009 herbicide Substances 0.000 claims 2
• 125000005842 heteroatom Chemical group 0.000 claims 2
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
• 125000004423 acyloxy group Chemical group 0.000 claims 1
• 230000002411 adverse Effects 0.000 claims 1
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
• 150000001244 carboxylic acid anhydrides Chemical class 0.000 claims 1
• 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
• 150000001733 carboxylic acid esters Chemical class 0.000 claims 1
• 125000000392 cycloalkenyl group Chemical group 0.000 claims 1
• 125000004438 haloalkoxy group Chemical group 0.000 claims 1
• 125000005843 halogen group Chemical group 0.000 claims 1
• 230000002363 herbicidal effect Effects 0.000 claims 1
• 125000001072 heteroaryl group Chemical group 0.000 claims 1
• 150000002431 hydrogen Chemical class 0.000 claims 1
• WRIRWRKPLXCTFD-UHFFFAOYSA-N malonamide Chemical compound NC(=O)CC(N)=O WRIRWRKPLXCTFD-UHFFFAOYSA-N 0.000 claims 1
• 238000004519 manufacturing process Methods 0.000 claims 1
• 231100000208 phytotoxic Toxicity 0.000 claims 1
• 230000000885 phytotoxic effect Effects 0.000 claims 1
• 239000003223 protective agent Substances 0.000 claims 1
• 238000009331 sowing Methods 0.000 claims 1
• 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
• 125000002947 alkylene group Chemical group 0.000 description 1
• 125000002619 bicyclic group Chemical group 0.000 description 1
• 125000004122 cyclic group Chemical group 0.000 description 1
• 125000002993 cycloalkylene group Chemical group 0.000 description 1
• 125000001047 cyclobutenyl group Chemical group C1(=CCC1)* 0.000 description 1
• 125000001162 cycloheptenyl group Chemical group C1(=CCCCCC1)* 0.000 description 1
• 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
• 125000000522 cyclooctenyl group Chemical group C1(=CCCCCCC1)* 0.000 description 1
• 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 1
• 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
• 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
• 125000002950 monocyclic group Chemical group 0.000 description 1
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 125000003518 norbornenyl group Chemical group C12(C=CC(CC1)C2)* 0.000 description 1
• 125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
• 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
• 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1