JP2009510201A5 - - Google Patents

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Publication number

JP2009510201A5

JP2009510201A5 JP2008532733A JP2008532733A JP2009510201A5 JP 2009510201 A5 JP2009510201 A5 JP 2009510201A5 JP 2008532733 A JP2008532733 A JP 2008532733A JP 2008532733 A JP2008532733 A JP 2008532733A JP 2009510201 A5 JP2009510201 A5 JP 2009510201A5

Authority

JP

Japan

Prior art keywords

carbon atoms

group

groups

alkyl

substituted

Prior art date

2006-09-21

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.)

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• 125000004432 carbon atom Chemical group C* 0.000 claims 47
• 125000000217 alkyl group Chemical group 0.000 claims 21
• 238000000034 method Methods 0.000 claims 15
• -1 hydroxy, amino Chemical group 0.000 claims 12
• 239000000654 additive Substances 0.000 claims 11
• 230000000996 additive effect Effects 0.000 claims 10
• 125000003277 amino group Chemical group 0.000 claims 9
• 229920001169 thermoplastic Polymers 0.000 claims 7
• 229920006395 saturated elastomer Polymers 0.000 claims 6
• 150000002894 organic compounds Chemical class 0.000 claims 5
• FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims 4
• 239000002253 acid Substances 0.000 claims 4
• 125000000753 cycloalkyl group Chemical group 0.000 claims 4
• 239000000155 melt Substances 0.000 claims 4
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 4
• 229920000768 polyamine Polymers 0.000 claims 4
• 239000000600 sorbitol Substances 0.000 claims 4
• KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims 3
• 125000003545 alkoxy group Chemical group 0.000 claims 3
• 125000003118 aryl group Chemical group 0.000 claims 3
• 210000000988 bone and bone Anatomy 0.000 claims 3
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 3
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 3
• 125000005842 heteroatom Chemical group 0.000 claims 3
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
• 239000007787 solid Substances 0.000 claims 3
• 125000002723 alicyclic group Chemical group 0.000 claims 2
• 125000001931 aliphatic group Chemical group 0.000 claims 2
• 150000001875 compounds Chemical class 0.000 claims 2
• 125000005843 halogen group Chemical group 0.000 claims 2
• 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
• 238000002844 melting Methods 0.000 claims 2
• 230000008018 melting Effects 0.000 claims 2
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
• 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims 2
• DKBCURTUXYMRFB-LXTVHRRPSA-N (2r,3r,4s,5r)-7-(3,4-dimethylphenyl)hept-6-ene-1,2,3,4,5,6-hexol Chemical compound CC1=CC=C(C=C(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO)C=C1C DKBCURTUXYMRFB-LXTVHRRPSA-N 0.000 claims 1
• 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 claims 1
• 125000003542 3-methylbutan-2-yl group Chemical group [H]C([H])([H])C([H])(*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
• 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 1
• 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 1
• 125000001960 7 membered carbocyclic group Chemical group 0.000 claims 1
• 150000007513 acids Chemical class 0.000 claims 1
• 125000003342 alkenyl group Chemical group 0.000 claims 1
• 125000003282 alkyl amino group Chemical group 0.000 claims 1
• 125000005332 alkyl sulfoxy group Chemical group 0.000 claims 1
• 125000004414 alkyl thio group Chemical group 0.000 claims 1
• 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 claims 1
• 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
• 125000002619 bicyclic group Chemical group 0.000 claims 1
• 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 claims 1
• 229910052799 carbon Inorganic materials 0.000 claims 1
• 238000005266 casting Methods 0.000 claims 1
• 238000002425 crystallisation Methods 0.000 claims 1
• 230000008025 crystallization Effects 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
• 230000001747 exhibiting effect Effects 0.000 claims 1
• 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims 1
• 125000000623 heterocyclic group Chemical group 0.000 claims 1
• 229910052739 hydrogen Inorganic materials 0.000 claims 1
• 239000001257 hydrogen Substances 0.000 claims 1
• 125000001165 hydrophobic group Chemical group 0.000 claims 1
• 150000002484 inorganic compounds Chemical class 0.000 claims 1
• 229910010272 inorganic material Inorganic materials 0.000 claims 1
• 230000003993 interaction Effects 0.000 claims 1
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
• 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
• 230000007774 longterm Effects 0.000 claims 1
• 238000004519 manufacturing process Methods 0.000 claims 1
• 238000010128 melt processing Methods 0.000 claims 1
• 238000002156 mixing Methods 0.000 claims 1
• 125000001624 naphthyl group Chemical group 0.000 claims 1
• 125000001326 naphthylalkyl group Chemical group 0.000 claims 1
• 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
• 125000004430 oxygen atom Chemical group O* 0.000 claims 1
• 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 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
• 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
• 229910052717 sulfur Inorganic materials 0.000 claims 1
• 125000004434 sulfur atom Chemical group 0.000 claims 1
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 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 claims 1