Detail of "19286-75-0"
- CAS Number:
- 19286-75-0
- Name:
9,10-Anthracenedione,1-hydroxy-4-(phenylamino)-
- Molecular Structure:
- Formula:
- C20H13 N O3
- Molecular Weight:
- 315.32212
- Deleted CAS:
- 12217-94-6|68858-89-9
- Synonyms:
- Anthraquinone,1-anilino-4-hydroxy- (6CI,7CI,8CI);1-(Phenylamino)-4-hydroxyanthraquinone;1-Hydroxy-4-(phenylamino)anthraquinone;1-Hydroxy-4-anilinoanthraquinone;C.I.60724;C.I. Disperse Violet 103;C.I. Disperse Violet 23;C.I. Disperse Violet27;C.I. Disperse Violet 30;C.I. Disperse Violet 37;Disperse Violet 103;Disperse Violet 27;Disperse Violet 37;Foron Brilliant Violet E-BL;ForonBrilliant Violet E-BLN;Latyl Violet BN;Miketon Polyester Violet BN;NSC118283;Sumikaron Violet E-RL;Sumikaron Violet R;Sumikaron Violet RL;
- Density:
- 1.41g/cm3
- Boiling Point:
- 507.2°Cat760mmHg
- Flash Point:
- 260.5°C
9,10-Anthracenedione,1-hydroxy-4-(phenylamino)-
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Reference
- Photochemical reactions of N-substituted 2-amino-1-acetoxy-9,10-anthraquinones
- Photochemical reactions of N-substituted 2-amino-1-acetoxy-9,10-anthraquinones. Russkikh, S. A.; Klimenko, L.Some commonly used reagents like 19286-75-0 is used in this experiment. S.; Gritsan, N. P.; Fokin, E. P. (Novosib. Inst. Org. Khim., Novosibirsk, USSR). Zh. Org. Khim., 20(9), 1949-56 (Russian) 1984. CODEN: ZORKAE. ISSN: 0514-7492. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) Photolysis of 9,10-anthraquinones I (R = NHAc, NMe2, piperidino; R1 = H, OAc, NHAc) with UV light at 77 K gave 1,10-anthraquinones II; these isomerizations were thermally reversible. Photolysis of I with visible light at 298 K gave anthra[2,1-d]oxazolines (e.g., III) and 2-(alkylamino)-1-hydroxy- and 2-(alkylformylamino)-1-hydroxy-9,10-anthraquinones in reversible processes. .