JP2009057460A5 - - Google Patents

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Publication number

JP2009057460A5

JP2009057460A5 JP2007225735A JP2007225735A JP2009057460A5 JP 2009057460 A5 JP2009057460 A5 JP 2009057460A5 JP 2007225735 A JP2007225735 A JP 2007225735A JP 2007225735 A JP2007225735 A JP 2007225735A JP 2009057460 A5 JP2009057460 A5 JP 2009057460A5

Authority

JP

Japan

Prior art keywords

alkyl

replaced

halogen

independently

hydrogen

Prior art date

2007-08-31

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

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• 125000000217 alkyl group Chemical group 0.000 claims description 17
• 150000001875 compounds Chemical class 0.000 claims description 13
• 125000004432 carbon atom Chemical group C* 0.000 claims description 11
• 229910052736 halogen Inorganic materials 0.000 claims description 9
• 150000002367 halogens Chemical class 0.000 claims description 9
• 229910052739 hydrogen Inorganic materials 0.000 claims description 9
• 239000001257 hydrogen Substances 0.000 claims description 9
• 239000004973 liquid crystal related substance Substances 0.000 claims description 8
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
• UWCWUCKPEYNDNV-LBPRGKRZSA-N 2,6-dimethyl-n-[[(2s)-pyrrolidin-2-yl]methyl]aniline Chemical compound CC1=CC=CC(C)=C1NC[C@H]1NCCC1 UWCWUCKPEYNDNV-LBPRGKRZSA-N 0.000 claims description 6
• 125000002947 alkylene group Chemical group 0.000 claims description 6
• 125000003118 aryl group Chemical group 0.000 claims description 4
• 229910052799 carbon Inorganic materials 0.000 claims description 2
• 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
• 125000001188 haloalkyl group Chemical group 0.000 claims description 2
• 150000002431 hydrogen Chemical class 0.000 claims description 2
• 125000003342 alkenyl group Chemical group 0.000 description 2
• 238000004364 calculation method Methods 0.000 description 2
• 230000000704 physical effect Effects 0.000 description 2
• 239000003795 chemical substances by application Substances 0.000 description 1
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([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
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
• 238000005259 measurement Methods 0.000 description 1
• 238000000691 measurement method Methods 0.000 description 1
• 238000000034 method Methods 0.000 description 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 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
• 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 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
• 238000006467 substitution reaction Methods 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