JP2010504386A5 - - Google Patents

Info

Publication number

JP2010504386A5

JP2010504386A5 JP2009528704A JP2009528704A JP2010504386A5 JP 2010504386 A5 JP2010504386 A5 JP 2010504386A5 JP 2009528704 A JP2009528704 A JP 2009528704A JP 2009528704 A JP2009528704 A JP 2009528704A JP 2010504386 A5 JP2010504386 A5 JP 2010504386A5

Authority

JP

Japan

Prior art keywords

composition

composition according

benzoxazine

component

formula

Prior art date

2007-09-18

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

• Espacenet
• Global Dossier
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• 239000000203 mixture Substances 0.000 claims description 53
• CMLFRMDBDNHMRA-UHFFFAOYSA-N 2h-1,2-benzoxazine Chemical compound C1=CC=C2C=CNOC2=C1 CMLFRMDBDNHMRA-UHFFFAOYSA-N 0.000 claims description 21
• 125000003118 aryl group Chemical group 0.000 claims description 18
• 125000000217 alkyl group Chemical group 0.000 claims description 15
• 239000003054 catalyst Substances 0.000 claims description 14
• 229910052739 hydrogen Inorganic materials 0.000 claims description 8
• 239000001257 hydrogen Substances 0.000 claims description 8
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
• 238000000576 coating method Methods 0.000 claims description 7
• 239000002184 metal Substances 0.000 claims description 7
• 229910052751 metal Inorganic materials 0.000 claims description 7
• 239000002685 polymerization catalyst Substances 0.000 claims description 7
• 239000000853 adhesive Substances 0.000 claims description 5
• 230000001070 adhesive effect Effects 0.000 claims description 5
• 239000000565 sealant Substances 0.000 claims description 5
• 239000004065 semiconductor Substances 0.000 claims description 4
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 3
• 239000011248 coating agent Substances 0.000 claims description 3
• 125000004122 cyclic group Chemical group 0.000 claims description 3
• 150000002739 metals Chemical class 0.000 claims description 3
• 229920000642 polymer Polymers 0.000 claims description 3
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
• 229910052794 bromium Inorganic materials 0.000 claims description 2
• 229910052799 carbon Inorganic materials 0.000 claims description 2
• 125000004432 carbon atom Chemical group C* 0.000 claims description 2
• 239000003795 chemical substances by application Substances 0.000 claims description 2
• 229910052801 chlorine Inorganic materials 0.000 claims description 2
• 229910052731 fluorine Inorganic materials 0.000 claims description 2
• 229910052736 halogen Inorganic materials 0.000 claims description 2
• 150000002367 halogens Chemical class 0.000 claims description 2
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
• 239000003446 ligand Substances 0.000 claims description 2
• 238000002360 preparation method Methods 0.000 claims description 2
• 125000001424 substituent group Chemical group 0.000 claims description 2
• 150000001875 compounds Chemical class 0.000 claims 1
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
• 0 Cc1c(*)c(*)c(CN(*)CO2)c2c1C Chemical compound Cc1c(*)c(*)c(CN(*)CO2)c2c1C 0.000 description 9
• 239000002904 solvent Substances 0.000 description 8
• 150000002576 ketones Chemical class 0.000 description 4
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
• 150000001298 alcohols Chemical class 0.000 description 2
• 150000001408 amides Chemical class 0.000 description 2
• 150000001491 aromatic compounds Chemical class 0.000 description 2
• 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 2
• 238000007334 copolymerization reaction Methods 0.000 description 2
• 150000002148 esters Chemical class 0.000 description 2
• 150000002170 ethers Chemical class 0.000 description 2
• JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-UHFFFAOYSA-N 0.000 description 2
• 239000000463 material Substances 0.000 description 2
• 229910044991 metal oxide Inorganic materials 0.000 description 2
• 150000004706 metal oxides Chemical class 0.000 description 2
• 239000002245 particle Substances 0.000 description 2
• 239000012255 powdered metal Substances 0.000 description 2
• HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
• 239000011256 inorganic filler Substances 0.000 description 1
• 229910003475 inorganic filler Inorganic materials 0.000 description 1
• 238000000034 method Methods 0.000 description 1
• 239000012766 organic filler Substances 0.000 description 1
• 229920000620 organic polymer Polymers 0.000 description 1
• 238000006116 polymerization reaction Methods 0.000 description 1
• 239000000843 powder Substances 0.000 description 1
• 150000004760 silicates Chemical class 0.000 description 1
• 239000000377 silicon dioxide Substances 0.000 description 1
• 239000000758 substrate Substances 0.000 description 1
• 239000002023 wood Substances 0.000 description 1