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4053-45-6

4053-45-6 Structure

4053-45-6 Structure
IdentificationBack Directory
[Name]

5-(CHLOROMETHYL)-8-QUINOLINOL HYDROCHLORIDE
[CAS]

4053-45-6
[Synonyms]

SKL220
Nsc83066
Aids125750
Aids-125750
IFLAB-BB F2124-0006
TIMTEC-BB SBB000700
5-(Chloromethyl)-8-quinolinol
8-quinolinol, 5-(chloromethyl)-
5-(CHLOROMETHYL)QUINOLIN-8-OL HYDROCHLORIDE
5-(CHLOROMETHYL)-8-QUINOLINOL HYDROCHLORIDE
8-Quinolinol, 5-(chloromethyl)-, hydrochloride
5-(Chloromethyl)-8-hydroxyquinoline hydrochloride
5-(Chloromethyl)quinolin-8-ol hydrochloride (1:1)
[Molecular Formula]

C10H9Cl2NO
[MDL Number]

MFCD01790514
[MOL File]

4053-45-6.mol
[Molecular Weight]

230.09
Chemical PropertiesBack Directory
[Melting point ]

280 °C (decomp)
[storage temp. ]

2-8°C
[EPA Substance Registry System]

8-Quinolinol, 5-(chloromethyl)-, hydrochloride (1:1) (4053-45-6)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

22
[TSCA ]

TSCA listed
[HazardClass ]

IRRITANT
[HS Code ]

2933499090
Hazard InformationBack Directory
[Synthesis]

8-Hydroxyquinoline

148-24-3

Formaldehyde

50-00-0

5-(CHLOROMETHYL)-8-QUINOLINOL HYDROCHLORIDE

4053-45-6

14.6 g (0.1 mol) of 8-hydroxyquinoline, 16 mL of 32% aqueous hydrochloric acid and 16 mL (0.1 mol) of 37% aqueous formaldehyde were mixed at 0°C and passed through hydrogen chloride gas to react for 6 hours. After completion of the reaction, the mixture was allowed to stand at room temperature for 2 hours without stirring. The yellow solid produced by the reaction was collected by filtration, washed with 90% ethanol and dried under vacuum to afford 5-(chloromethyl)-8-quinolinol hydrochloride (19.0 g, 98% yield). The structure of the product was confirmed by 1H NMR (250 MHz, CDCl3): δ 5.32 (s, 2H), 7.53 (m, 1H), 7.85 (m, 2H), 8.12 (m, 1H), 9.12 (m, 1H), 9.28 (m, 1H).

[References]

[1] Journal of Medicinal Chemistry, 2014, vol. 57, # 24, p. 10455 - 10463
[2] Bioorganic and Medicinal Chemistry, 2005, vol. 13, # 3, p. 773 - 783
[3] Patent: WO2012/20389, 2012, A1. Location in patent: Page/Page column 22
[4] Journal of Medicinal Chemistry, 2015, vol. 58, # 21, p. 8616 - 8637
[5] Journal of Molecular Liquids, 2016, vol. 219, p. 396 - 404
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