Detail of "16862-11-6"

CAS Number:
16862-11-6
Name:
8-Quinolinol,hydrochloride (1:1)
Molecular Structure:
Formula:
C₉H₈ClNO
Molecular Weight:
181.62
Synonyms:
8-Quinolinol,hydrochloride (8CI,9CI);8-Hydroxyquinoline hydrochloride;Oxine hydrochloride;Quinolin-8-ol hydrochloride (1:1);Quinolin-8-ol HCl;
EINECS:
240-884-7
Melting Point:
179-184 °C
Boiling Point:
267 °C at 760 mmHg
Flash Point:
143.1 °C
Appearance:
Yellow crystal powder

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Effect of metal salts in prolonging antibacterial activity of teeth treated with 8-hydroxyquinoline: Effect of metal salts in prolonging antibacterial activity of teeth treated with 8-hydroxyquinoline. Greenberg, Joshua; Turesky, Samuel S.; Warner, Victor D. (Sch. Dent. Med., Tufts Univ., Boston, Mass., USA). J. Periodontol. 7487-88-9 and 7447-39-4 are cas registry numbers of chemicals which are used as reagents here., 47(11), 664-6 (English) 1976. CODEN: JOPRAJ. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) Pretreatment of extd. teeth with FeSO4, Fe2(SO4)3, FeCl3, and CuCl2 prolonged the antibacterial activity of 8-hydroxyquinoline-HCl (I) [16862-11-6]. The iron sulfates were particularly effective. .

Role of water structure and its alteration by various electrolytes in heavy water production: Role of water structure and its alteration by various electrolytes in heavy water production. Pradhan, D. G. (Dhenkanal, India). Indian J. Chem., Sect. A, 14(10), 793-4 (English) 1976.Several reagents with their cas registry numbers 16862-11-6 and 13330-15-9 are used here. CODEN: IJCADU. DOCUMENT TYPE: Journal CA Section: 71 (Nuclear Technology) Section cross-reference(s): 65 The role of H2O structure and its alteration by various solutes such as quinoline hydrochloride, 8-nitroquinoline, 8-hydroxyquinoline hydrochloride, and 2-methylquinoline were studied with a view to developing a method for heavy water prodn. 8-Hydroxyquinoline hydrochloride and 2-methylquinoline hydrochlode enrich the D content in the 1st fraction of distillate and hence are termed as structure-making solutes. 8-Nitroquinoline hydrochloride causes redn. in the D content in the 1st fraction and hence has beentermed as structure-breaking. Quinoline hydrochloride has marginal structure-breaking properties. This difference in the behavior of the org. bases is attributed to the difference in the charge d. on a N atom due to the presence of e-withdrawing or e-donating groups. .