JP2009108302A5 - - Google Patents

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Publication number

JP2009108302A5

JP2009108302A5 JP2008238573A JP2008238573A JP2009108302A5 JP 2009108302 A5 JP2009108302 A5 JP 2009108302A5 JP 2008238573 A JP2008238573 A JP 2008238573A JP 2008238573 A JP2008238573 A JP 2008238573A JP 2009108302 A5 JP2009108302 A5 JP 2009108302A5

Authority

JP

Japan

Prior art keywords

optionally substituted

formula

integer

alkyl

hydrogen

Prior art date

2008-09-17

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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• 229910052739 hydrogen Inorganic materials 0.000 claims 22
• 239000001257 hydrogen Substances 0.000 claims 22
• 125000000217 alkyl group Chemical group 0.000 claims 19
• 150000002431 hydrogen Chemical class 0.000 claims 19
• 238000004132 cross linking Methods 0.000 claims 17
• 239000004033 plastic Substances 0.000 claims 10
• 229920003023 plastic Polymers 0.000 claims 10
• 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 9
• 125000004093 cyano group Chemical group *C#N 0.000 claims 9
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 8
• 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 8
• 239000011737 fluorine Substances 0.000 claims 8
• 229910052731 fluorine Inorganic materials 0.000 claims 8
• -1 pyrrolidino, piperidino Chemical group 0.000 claims 8
• 150000001875 compounds Chemical class 0.000 claims 7
• 239000000203 mixture Substances 0.000 claims 7
• 238000004519 manufacturing process Methods 0.000 claims 6
• 238000000034 method Methods 0.000 claims 6
• 125000003118 aryl group Chemical group 0.000 claims 5
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 5
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
• 239000004594 Masterbatch (MB) Substances 0.000 claims 4
• 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 4
• PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims 4
• 230000001588 bifunctional effect Effects 0.000 claims 4
• 239000000460 chlorine Substances 0.000 claims 4
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
• 125000003545 alkoxy group Chemical group 0.000 claims 3
• 229910052801 chlorine Inorganic materials 0.000 claims 3
• 238000004040 coloring Methods 0.000 claims 3
• 125000000753 cycloalkyl group Chemical group 0.000 claims 3
• 239000000975 dye Substances 0.000 claims 3
• 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 3
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 3
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
• 229910052794 bromium Inorganic materials 0.000 claims 2
• 125000001309 chloro group Chemical group Cl* 0.000 claims 2
• 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
• 238000006116 polymerization reaction Methods 0.000 claims 2
• 239000002994 raw material Substances 0.000 claims 2
• NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims 1
• OMJKVIFSWSQTGQ-UHFFFAOYSA-N 6,7-bis(aziridin-1-yl)quinazoline-5,8-dione Chemical compound C1CN1C=1C(=O)C2=NC=NC=C2C(=O)C=1N1CC1 OMJKVIFSWSQTGQ-UHFFFAOYSA-N 0.000 claims 1
• KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 1
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
• BTIIGNUPPKUQAP-UHFFFAOYSA-N [1-[2,3-dihydroxy-4-[4-(oxoazaniumylmethylidene)pyridin-1-yl]butyl]pyridin-4-ylidene]methyl-oxoazanium;diperchlorate Chemical compound [O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O.C1=CC(=C[NH+]=O)C=CN1CC(O)C(O)CN1C=CC(=C[NH+]=O)C=C1 BTIIGNUPPKUQAP-UHFFFAOYSA-N 0.000 claims 1
• 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims 1
• PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims 1
• 150000002148 esters Chemical class 0.000 claims 1
• 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 1
• 239000004615 ingredient Substances 0.000 claims 1
• 239000012948 isocyanate Substances 0.000 claims 1
• 150000002513 isocyanates Chemical class 0.000 claims 1
• 239000001048 orange dye Substances 0.000 claims 1
• 229910052760 oxygen Inorganic materials 0.000 claims 1
• 238000002360 preparation method Methods 0.000 claims 1
• 239000001044 red dye Substances 0.000 claims 1
• 229910052717 sulfur Inorganic materials 0.000 claims 1
• 239000012209 synthetic fiber Substances 0.000 claims 1
• 229920002994 synthetic fiber Polymers 0.000 claims 1
• CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims 1
• 0 *Oc(c(C(c1c2cccc1)=O)c1C2=O)cc(Sc(c(N)c2C(c3c4cccc3)=O)cc(O*)c2C4=O)c1N Chemical compound *Oc(c(C(c1c2cccc1)=O)c1C2=O)cc(Sc(c(N)c2C(c3c4cccc3)=O)cc(O*)c2C4=O)c1N 0.000 description 2
• FZERHIULMFGESH-UHFFFAOYSA-N CC(Nc1ccccc1)=O Chemical compound CC(Nc1ccccc1)=O FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 1