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5,6,7,8-Tetrahydroquinoline

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5,6,7,8-Tetrahydroquinoline Basic information

Product Name:
5,6,7,8-Tetrahydroquinoline
Synonyms:
  • 5,6,7,8-Tetrahydroquinoline ,98%
  • 5,6,7,8- fourhydrogenation ofquinoline
  • 25G/100G/1KG
  • quinoline,5,6,7,8-tetrahydro-
  • 2,3-CYCLOHEXENO PYRIDINE
  • 5,6,7,8-TETRAHYDROQUINOLINE
  • 2,3-CYCLOHEXANO PYRIDINE
  • 5,6,7,8-Tetrahydroquinoline97%
CAS:
10500-57-9
MF:
C9H11N
MW:
133.19
EINECS:
234-030-2
Product Categories:
  • API intermediates
  • Quinoline Derivertives
  • Quinoline&Isoquinoline
Mol File:
10500-57-9.mol
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5,6,7,8-Tetrahydroquinoline Chemical Properties

Boiling point:
238°C
Density 
1,08 g/cm3
refractive index 
1.5420 to 1.5450
Flash point:
90°C
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform (Slightly), DMSO (Sparingly) Methanol (Slightly)
form 
Oil
pka
6.30±0.20(Predicted)
color 
Colourless
Specific Gravity
1.0341.0304 (20/4℃)
InChI
InChI=1S/C9H11N/c1-2-6-9-8(4-1)5-3-7-10-9/h3,5,7H,1-2,4,6H2
InChIKey
YQDGQEKUTLYWJU-UHFFFAOYSA-N
SMILES
N1C2=C(CCCC2)C=CC=1
CAS DataBase Reference
10500-57-9(CAS DataBase Reference)
NIST Chemistry Reference
Quinoline, 5,6,7,8-tetrahydro-(10500-57-9)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-20/21/22
Safety Statements 
26-36/37/39-37/39
HS Code 
29334900
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5,6,7,8-Tetrahydroquinoline Usage And Synthesis

Chemical Properties

Colorless to light yellow liquid

Uses

5,6,7,8-Tetrahydroquinoline can be used to prevent and treat of hyperlipemia.

Synthesis

5,6,7,8-Tetrahydroquinoline is prepared by the reaction of pyridine and 1,4-dichlorobutane. The specific synthesis steps are as follows:
At 25℃ and an inert atmosphere,Compound 2 (2.67 g, 21.02 mmol) was added to a suspension of aluminum chloride (0.20 g, 1.5 mmol) in pyridine (10 mL). After stirring the obtained orange solution for 24 hours, It was poured into an ice water mixture (50 g) and extracted with ethyl acetate (50 mL).The organic layer was separated and washed sequentially with water (50 mL). The organic layer was washed with saturated sodium bicarbonate solution (50 mL) and brine (50 mL). It was then dried over NaSO4 and concentrated in vacuo. The yellow oil was subjected to flash chromatography on silica gel (eluent: hexane), Obtaining 5,6,7,8-tetrahydroquinoline, 2.66 g, yield 95%.

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