ChemicalBook--->CAS DataBase List--->14631-46-0

14631-46-0

14631-46-0 Structure

14631-46-0 Structure
IdentificationBack Directory
[Name]

5,6,7,8-Tetrahydroquinolin-8-ol
[CAS]

14631-46-0
[Synonyms]

in-8-oL
Tetrahydro-quinolin-8-ol
5,6,7,8-tetrahydro-8-Quinolinol
5,6,7,8-TETRAHYDRO-QUINOLIN-8-OL
8-quinolinol,5,6,7,8-tetrahydro-
5,6,7,8-Tetrahydroquinoline-8-ol
5,6,7,8-Tetrahydroquinolin-8-ol ISO 9001:2015 REACH
[Molecular Formula]

C9H11NO
[MDL Number]

MFCD07369987
[MOL File]

14631-46-0.mol
[Molecular Weight]

149.19
Chemical PropertiesBack Directory
[Melting point ]

64-65 °C
[Boiling point ]

88-96 °C(Press: 2 Torr)
[density ]

1.179±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[form ]

solid
[pka]

13.44±0.20(Predicted)
[Appearance]

Off-white to yellow Solid
[InChI]

1S/C9H11NO/c11-8-5-1-3-7-4-2-6-10-9(7)8/h2,4,6,8,11H,1,3,5H2
[InChIKey]

YCQHYOBSOVFBEB-UHFFFAOYSA-N
[SMILES]

OC1CCCc2cccnc12
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[RIDADR ]

UN2811
[WGK Germany ]

WGK 3
[HazardClass ]

6.1
[HS Code ]

2933499090
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Hazard InformationBack Directory
[Chemical Properties]

off-white crytalline
[Synthesis Reference(s)]

Journal of Heterocyclic Chemistry, 15, p. 249, 1978 DOI: 10.1002/jhet.5570150213
[Synthesis]

2-Chloro-5,6,7,8-tetrahydro-8-quinolinol

130861-73-3

5,6,7,8-Tetrahydroquinolin-8-ol

14631-46-0

General procedure for the synthesis of 5,6,7,8-tetrahydro-8-hydroxyquinolines from 2-chloro-5,6,7,8-tetrahydroquinolin-8-ol: a generalized method was employed using PdCl2 (dppf), PdCl2 (tbpf), or (A.caPhos) PdCl2 as catalyst. First, the halogenated heterocyclic compound (0.66 mmol) was dissolved in anhydrous THF (13.2 mL) and degassed by drumming argon for a few minutes. Subsequently, PdCl2 (dppf) (27.0 mg, 0.033 mmol, 5.0 mol%), TMEDA (0.130 g, 1.12 mmol, 1.7 equiv) and NaBH4 (42.4 mg, 1.12 mmol, 1.7 equiv) were added sequentially. The reaction mixture was stirred under argon protection at room temperature for an appropriate time, after which it was post-treated as described above.

[References]

[1] Tetrahedron Letters, 2010, vol. 51, # 12, p. 1562 - 1565
[2] Journal of Molecular Catalysis A: Chemical, 2014, vol. 393, p. 191 - 209
Spectrum DetailBack Directory
[Spectrum Detail]

5,6,7,8-Tetrahydroquinolin-8-ol(14631-46-0)1HNMR
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