JPS57177057A - Fluoran compound - Google Patents

Info

Publication number

JPS57177057A

JPS57177057A JP56061258A JP6125881A JPS57177057A JP S57177057 A JPS57177057 A JP S57177057A JP 56061258 A JP56061258 A JP 56061258A JP 6125881 A JP6125881 A JP 6125881A JP S57177057 A JPS57177057 A JP S57177057A

Authority

JP

Japan

Prior art keywords

compound

cyclohexyl

methyl

lower alkyl

toluene

Prior art date

1981-04-24

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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• -1 Fluoran compound Chemical class 0.000 title abstract 2
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 6
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
• 125000000217 alkyl group Chemical group 0.000 abstract 2
• WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 2
• 238000004040 coloring Methods 0.000 abstract 2
• 150000001875 compounds Chemical class 0.000 abstract 2
• DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 abstract 2
• 239000000463 material Substances 0.000 abstract 2
• 239000005711 Benzoic acid Substances 0.000 abstract 1
• 239000007864 aqueous solution Substances 0.000 abstract 1
• 235000010233 benzoic acid Nutrition 0.000 abstract 1
• 239000012965 benzophenone Substances 0.000 abstract 1
• 239000003795 chemical substances by application Substances 0.000 abstract 1
• 239000000975 dye Substances 0.000 abstract 1
• 239000005457 ice water Substances 0.000 abstract 1
• 238000000034 method Methods 0.000 abstract 1
• 239000002243 precursor Substances 0.000 abstract 1
• 239000011541 reaction mixture Substances 0.000 abstract 1
• QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 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 abstract 1