ChemicalBook > CAS DataBase List > 2-chloro-5,6,7,8-tetrahydroquinoline

2-chloro-5,6,7,8-tetrahydroquinoline

Product Name
2-chloro-5,6,7,8-tetrahydroquinoline
CAS No.
21172-88-3
Chemical Name
2-chloro-5,6,7,8-tetrahydroquinoline
Synonyms
2-chloro-5,6,7,8-tetrahydroquinoline;Quinoline, 2-chloro-5,6,7,8-tetrahydro-
CBNumber
CB31557823
Molecular Formula
C9H10ClN
Formula Weight
167.64
MOL File
21172-88-3.mol
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2-chloro-5,6,7,8-tetrahydroquinoline Property

Melting point:
93-95 °C
Boiling point:
260℃
Density 
1.185
Flash point:
136℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
1.46±0.20(Predicted)
Appearance
Colorless to light yellow Liquid
InChI
InChI=1S/C9H10ClN/c10-9-6-5-7-3-1-2-4-8(7)11-9/h5-6H,1-4H2
InChIKey
ZUXMRCHYHAWERW-UHFFFAOYSA-N
SMILES
N1C2=C(CCCC2)C=CC=1Cl
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Safety

HS Code 
2933499090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
C433328
Product name
2-Chloro-5,6,7,8-tetrahydroquinoline
Packaging
20mg
Price
$45
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC141269
Product name
2-Chloro-5,6,7,8-tetrahydroquinoline
Packaging
25mg
Price
$60
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC141269
Product name
2-Chloro-5,6,7,8-tetrahydroquinoline
Packaging
50mg
Price
$100
Updated
2021/12/16
AK Scientific
Product number
Z4404
Product name
2-Chloro-5,6,7,8-tetrahydroquinoline
Packaging
100mg
Price
$103
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC141269
Product name
2-Chloro-5,6,7,8-tetrahydroquinoline
Packaging
100mg
Price
$150
Updated
2021/12/16
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2-chloro-5,6,7,8-tetrahydroquinoline Chemical Properties,Usage,Production

Synthesis

54802-19-6

21172-88-3

The general procedure for the synthesis of 2-chloro-5,6,7,8-tetrahydroquinoline from 5,6,7,8-tetrahydro-2-quinolinone is as follows: 1. 20 g (0.134 mol) of 5,6,7,8-tetrahydro-2-quinolinone was added to a 250 mL two-necked flask with 28.8 mL (0.38 mol) of phosphorus trichloride (molar ratio 1:2.3) under dry conditions. 2. The reaction was rapidly stirred and heated to 135 °C and kept at reflux for 16 hours. 3. Upon completion of the reaction, the reaction mixture was cooled to 60-80 °C and then slowly poured under vigorous stirring into a 0.1% (W/V) sodium hydroxide solution pre-cooled to 0-5 °C to adjust the pH to 8.5. 4. Extract twice with 250 mL of dichloromethane at 0 °C and combine the organic phases. 5. Concentrate the organic phase by rotary evaporation to obtain the crude product. 6. The crude product was subjected to reduced pressure distillation at a pressure of 12-15 mmHg and the fractions with boiling ranges of 135-137 °C were collected to afford 20.3 g of colorless to pale yellow 2-chloro-5,6,7,8-tetrahydroquinoline liquid in 90% yield.

References

[1] Patent: CN103992270, 2016, B. Location in patent: Paragraph 0030-0033
[2] Patent: WO2006/35967, 2006, A1. Location in patent: Page/Page column 86

2-chloro-5,6,7,8-tetrahydroquinoline Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from 2-chloro-5,6,7,8-tetrahydroquinoline manufacturers

Career Henan Chemical Co
Product
2-chloro-5,6,7,8-tetrahydroquinoline 21172-88-3
Price
US $7.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
100KG
Release date
2019-07-12