JP2009534302A5 - - Google Patents

Info

Publication number

JP2009534302A5

JP2009534302A5 JP2009500917A JP2009500917A JP2009534302A5 JP 2009534302 A5 JP2009534302 A5 JP 2009534302A5 JP 2009500917 A JP2009500917 A JP 2009500917A JP 2009500917 A JP2009500917 A JP 2009500917A JP 2009534302 A5 JP2009534302 A5 JP 2009534302A5

Authority

JP

Japan

Prior art keywords

formula

compound

alkyl

methyl

iso

Prior art date

2007-03-21

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.)

Pending

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• 150000001875 compounds Chemical class 0.000 claims 18
• 125000000217 alkyl group Chemical group 0.000 claims 11
• 239000001257 hydrogen Substances 0.000 claims 9
• 229910052739 hydrogen Inorganic materials 0.000 claims 9
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 8
• 150000002431 hydrogen Chemical class 0.000 claims 5
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 4
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
• 125000000753 cycloalkyl group Chemical group 0.000 claims 4
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 3
• 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 3
• 125000003342 alkenyl group Chemical group 0.000 claims 3
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 3
• 238000009472 formulation Methods 0.000 claims 3
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 3
• 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 3
• 239000000203 mixture Substances 0.000 claims 3
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 3
• 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims 3
• 229910052757 nitrogen Inorganic materials 0.000 claims 3
• 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
• 125000001424 substituent group Chemical group 0.000 claims 3
• 125000003725 azepanyl group Chemical group 0.000 claims 2
• 238000000034 method Methods 0.000 claims 2
• 125000002757 morpholinyl group Chemical group 0.000 claims 2
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
• 239000002904 solvent Substances 0.000 claims 2
• 239000004094 surface-active agent Substances 0.000 claims 2
• 230000001988 toxicity Effects 0.000 claims 2
• 231100000419 toxicity Toxicity 0.000 claims 2
• -1 1,3 - dimethylbutyl Chemical group 0.000 claims 1
• 241000257303 Hymenoptera Species 0.000 claims 1
• DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical group [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims 1
• 239000003905 agrochemical Substances 0.000 claims 1
• 125000003545 alkoxy group Chemical group 0.000 claims 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 claims 1
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
• 239000004615 ingredient Substances 0.000 claims 1
• 125000005468 isobutylenyl group Chemical group 0.000 claims 1
• JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 claims 1
• 125000003386 piperidinyl group Chemical group 0.000 claims 1
• 125000005936 piperidyl group Chemical group 0.000 claims 1
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
• 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
• 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
• 235000019333 sodium laurylsulphate Nutrition 0.000 claims 1