JP2002363280A5 - - Google Patents

Info

Publication number

JP2002363280A5

JP2002363280A5 JP2001177493A JP2001177493A JP2002363280A5 JP 2002363280 A5 JP2002363280 A5 JP 2002363280A5 JP 2001177493 A JP2001177493 A JP 2001177493A JP 2001177493 A JP2001177493 A JP 2001177493A JP 2002363280 A5 JP2002363280 A5 JP 2002363280A5

Authority

JP

Japan

Prior art keywords

group

polyamide

formula

alkyl

represented

Prior art date

2001-06-12

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

Links

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• 239000004952 Polyamide Substances 0.000 description 44
• 229920002647 polyamide Polymers 0.000 description 44
• 125000000217 alkyl group Chemical group 0.000 description 32
• 239000004973 liquid crystal related substance Substances 0.000 description 24
• 239000003795 chemical substances by application Substances 0.000 description 20
• 239000002966 varnish Substances 0.000 description 20
• 125000004432 carbon atom Chemical group C* 0.000 description 16
• 125000000962 organic group Chemical group 0.000 description 14
• 125000003118 aryl group Chemical group 0.000 description 12
• 229910052760 oxygen Inorganic materials 0.000 description 12
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 12
• 125000002723 alicyclic group Chemical group 0.000 description 8
• 125000002947 alkylene group Chemical group 0.000 description 8
• 150000001875 compounds Chemical class 0.000 description 8
• 125000004122 cyclic group Chemical group 0.000 description 8
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 8
• 125000000623 heterocyclic group Chemical group 0.000 description 8
• URLKBWYHVLBVBO-UHFFFAOYSA-N Cc1ccc(C)cc1 Chemical compound Cc1ccc(C)cc1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 6
• 0 CC(N(*)c1ccc(C)cc1)=O Chemical compound CC(N(*)c1ccc(C)cc1)=O 0.000 description 4
• 125000003545 alkoxy group Chemical group 0.000 description 4
• 125000003368 amide group Chemical group 0.000 description 4
• 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 4
• 125000003709 fluoroalkyl group Chemical group 0.000 description 4
• 229910052736 halogen Inorganic materials 0.000 description 4
• 150000002367 halogens Chemical class 0.000 description 4
• 229910052739 hydrogen Inorganic materials 0.000 description 4
• 229910052698 phosphorus Inorganic materials 0.000 description 4
• 229920000642 polymer Polymers 0.000 description 4
• 125000002345 steroid group Chemical group 0.000 description 4
• 125000001424 substituent group Chemical group 0.000 description 4
• MGDNHIJGIWHQBL-UHFFFAOYSA-N CCN(C)C(C)=O Chemical compound CCN(C)C(C)=O MGDNHIJGIWHQBL-UHFFFAOYSA-N 0.000 description 2
• 239000004642 Polyimide Substances 0.000 description 2
• KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
• 229920005575 poly(amic acid) Polymers 0.000 description 2
• 229920001721 polyimide Polymers 0.000 description 2
• ZMYCGFKAPZHNPC-UHFFFAOYSA-N CC(N(C)c1ccc(C)cc1)=O Chemical compound CC(N(C)c1ccc(C)cc1)=O ZMYCGFKAPZHNPC-UHFFFAOYSA-N 0.000 description 1
• WLECPEWQOMTQOI-UHFFFAOYSA-N CCN(C(C)=O)c1ccc(C)cc1 Chemical compound CCN(C(C)=O)c1ccc(C)cc1 WLECPEWQOMTQOI-UHFFFAOYSA-N 0.000 description 1
• 101000634526 Homo sapiens Nucleolar pre-ribosomal-associated protein 1 Proteins 0.000 description 1
• 102100029053 Nucleolar pre-ribosomal-associated protein 1 Human genes 0.000 description 1
• UHOVQNZJYSORNB-UHFFFAOYSA-N c1ccccc1 Chemical compound c1ccccc1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
• 230000000052 comparative effect Effects 0.000 description 1
• 230000000694 effects Effects 0.000 description 1