JP2013234139A5 - - Google Patents

Info

Publication number

JP2013234139A5

JP2013234139A5 JP2012106828A JP2012106828A JP2013234139A5 JP 2013234139 A5 JP2013234139 A5 JP 2013234139A5 JP 2012106828 A JP2012106828 A JP 2012106828A JP 2012106828 A JP2012106828 A JP 2012106828A JP 2013234139 A5 JP2013234139 A5 JP 2013234139A5

Authority

JP

Japan

Prior art keywords

group

methyl

nonanol

octanol

heptanol

Prior art date

2012-05-08

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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• SJWFXCIHNDVPSH-UHFFFAOYSA-N octan-2-ol Chemical compound CCCCCCC(C)O SJWFXCIHNDVPSH-UHFFFAOYSA-N 0.000 description 4
• BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 3
• 125000004432 carbon atom Chemical group C* 0.000 description 3
• CETWDUZRCINIHU-UHFFFAOYSA-N 2-heptanol Chemical compound CCCCCC(C)O CETWDUZRCINIHU-UHFFFAOYSA-N 0.000 description 2
• NGDNVOAEIVQRFH-UHFFFAOYSA-N 2-nonanol Chemical compound CCCCCCCC(C)O NGDNVOAEIVQRFH-UHFFFAOYSA-N 0.000 description 2
• WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 description 2
• QNVRIHYSUZMSGM-UHFFFAOYSA-N hexan-2-ol Chemical compound CCCCC(C)O QNVRIHYSUZMSGM-UHFFFAOYSA-N 0.000 description 2
• 125000001183 hydrocarbyl group Chemical group 0.000 description 2
• ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
• JYVLIDXNZAXMDK-UHFFFAOYSA-N pentan-2-ol Chemical compound CCCC(C)O JYVLIDXNZAXMDK-UHFFFAOYSA-N 0.000 description 2
• ACUZDYFTRHEKOS-SNVBAGLBSA-N 2-Decanol Natural products CCCCCCCC[C@@H](C)O ACUZDYFTRHEKOS-SNVBAGLBSA-N 0.000 description 1
• QNVRIHYSUZMSGM-LURJTMIESA-N 2-Hexanol Natural products CCCC[C@H](C)O QNVRIHYSUZMSGM-LURJTMIESA-N 0.000 description 1
• 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
• GUHWHNUGIGOSCN-UHFFFAOYSA-N 4-Methyl-2-heptanol Chemical compound CCCC(C)CC(C)O GUHWHNUGIGOSCN-UHFFFAOYSA-N 0.000 description 1
• KZUBXUKRWLMPIO-UHFFFAOYSA-N 4-methylhexan-2-ol Chemical compound CCC(C)CC(C)O KZUBXUKRWLMPIO-UHFFFAOYSA-N 0.000 description 1
• GENRWSDYODERST-UHFFFAOYSA-N 4-methylnonan-2-ol Chemical compound CCCCCC(C)CC(C)O GENRWSDYODERST-UHFFFAOYSA-N 0.000 description 1
• FYMBAYNKBWGEIK-UHFFFAOYSA-N 5-methylheptan-2-ol Chemical compound CCC(C)CCC(C)O FYMBAYNKBWGEIK-UHFFFAOYSA-N 0.000 description 1
• ZDVJGWXFXGJSIU-UHFFFAOYSA-N 5-methylhexan-2-ol Chemical compound CC(C)CCC(C)O ZDVJGWXFXGJSIU-UHFFFAOYSA-N 0.000 description 1
• KZTLXVUOEODDMR-UHFFFAOYSA-N 5-methylnonan-2-ol Chemical compound CCCCC(C)CCC(C)O KZTLXVUOEODDMR-UHFFFAOYSA-N 0.000 description 1
• OYTRLQQQIHEJFE-UHFFFAOYSA-N 6-methylnonan-2-ol Chemical compound CCCC(C)CCCC(C)O OYTRLQQQIHEJFE-UHFFFAOYSA-N 0.000 description 1
• IBCSSJYUKOBWLB-UHFFFAOYSA-N 6-methyloctan-2-ol Chemical compound CCC(C)CCCC(C)O IBCSSJYUKOBWLB-UHFFFAOYSA-N 0.000 description 1
• LPTWGVWNFGQDPV-UHFFFAOYSA-N CC(CCC(C)O)CCC.CC(CC(C)O)CCCC Chemical compound CC(CCC(C)O)CCC.CC(CC(C)O)CCCC LPTWGVWNFGQDPV-UHFFFAOYSA-N 0.000 description 1
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• ACUZDYFTRHEKOS-UHFFFAOYSA-N decan-2-ol Chemical compound CCCCCCCCC(C)O ACUZDYFTRHEKOS-UHFFFAOYSA-N 0.000 description 1
• 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
• 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([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
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
• QQZOPKMRPOGIEB-UHFFFAOYSA-N n-butyl methyl ketone Natural products CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 1
• 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
• 150000003333 secondary alcohols Chemical class 0.000 description 1
• 125000003944 tolyl group Chemical group 0.000 description 1