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4-Chloro-6-hydroxyquinoline

Product Name
4-Chloro-6-hydroxyquinoline
CAS No.
148018-29-5
Chemical Name
4-Chloro-6-hydroxyquinoline
Synonyms
4-Chloroquinolin-6-ol;4-Chloro-6-quinolinol;6-Quinolinol, 4-chloro-;4-Chloro-6-hydroxyquinoline;4-chloroquinolin-6-ol - [C20033]
CBNumber
CB7947809
Molecular Formula
C9H6ClNO
Formula Weight
179.6
MOL File
148018-29-5.mol
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4-Chloro-6-hydroxyquinoline Property

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
Off-white to gray Solid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
C588118
Product name
4-Chloro-6-hydroxyquinoline
Packaging
10mg
Price
$60
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC137486
Product name
4-Chloro-6-hydroxyquinoline
Packaging
100mg
Price
$75
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC137486
Product name
4-Chloro-6-hydroxyquinoline
Packaging
250mg
Price
$130
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC137486
Product name
4-Chloro-6-hydroxyquinoline
Packaging
500mg
Price
$210
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC137486
Product name
4-Chloro-6-hydroxyquinoline
Packaging
1g
Price
$320
Updated
2021/12/16
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4-Chloro-6-hydroxyquinoline Chemical Properties,Usage,Production

Synthesis

4295-04-9

148018-29-5

General procedure for the synthesis of 4-chloro-6-hydroxyquinoline from 4-chloro-6-methoxyquinoline: 1. Synthesis of 4-chloro-6-hydroxyquinoline: To a stirred solution of 4-chloro-6-methoxyquinoline (500 mg, 2.5 mmol) in dichloromethane (DCM, 10 mL) was added an aqueous solution of hydriodic acid (HI) (5 mL, 45%). The reaction mixture was heated to 100 °C and stirred for 5 hours. Upon completion of the reaction, the solution was cooled to room temperature and diluted by adding water (20 mL). The organic phase was separated, the aqueous phase was alkalized and extracted with dichloromethane (DCM, 30 mL x 3). The organic phases were combined, washed sequentially with water and brine, dried over anhydrous sodium sulfate (Na2SO4), filtered, and concentrated in vacuum to give 4-chloro-6-hydroxyquinoline (300 mg, 67% yield) as a white solid, which was used directly in the next step of the reaction. lc-MS (ESI) m/z = 180.3 ([M + H]+). 2. Synthesis of 2-((4-chloroquinolin-6-yl)oxy)acetonitrile: Bromoacetonitrile (240 mg, 2.0 mmol) and cesium carbonate (Cs2CO3, 350 mg, 2.5 mmol) were added to a solution of 4-chloro-6-hydroxyquinoline (300 mg, 1.7 mmol) obtained above in N,N-dimethylformamide (DMF, 10 mL). The reaction mixture was heated to 60 °C and stirred for 3 hours. After the reaction was completed, the solution was cooled to room temperature and diluted by adding water (50 mL). It was extracted with ethyl acetate (EtOAc, 50 mL x 3), and the organic phases were combined, washed sequentially with water and brine, dried over anhydrous sodium sulfate (Na2SO4), filtered, and concentrated in vacuo to give 2-((4-chloroquinolin-6-yl)oxy)acetonitrile (300 mg, 81% yield) as an off-white solid. lc-MS (ESI) m/z = 219.1 ([M + H]+) . 3. The target product 30 was obtained as an off-white solid by using 2-((4-chloroquinolin-6-yl)oxy)acetonitrile in step 1 according to General Method A. 1H NMR (400 MHz, CD3OD) δ 8.49 (d, J = 4.9 Hz, 1H), 7.95 (d, J = 9.2 Hz, 1H), 7.65 (d, J = 2.8 Hz, 1H). 7.51 (dd, J = 9.2,3.0 Hz, 1H), 7.44 (d, J = 4.4 Hz, 1H), 5.20 (s, 2H), 2.97-3.02 (m, 2H), 2.27-2.41 (m, 3H), 2.05-2.08 (m, 1H).LC-MS (ESI) m/z = 313.1 ([M - H]-).

References

[1] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 2, p. 277 - 282
[2] Journal of the American Chemical Society, 1947, vol. 69, p. 1659,1660
[3] Justus Liebigs Annalen der Chemie, 1950, vol. 568, p. 73,79
[4] Patent: US5506235, 1996, A
[5] Patent: KR2016/6207, 2016, A. Location in patent: Paragraph 0516; 0519-0522

4-Chloro-6-hydroxyquinoline Preparation Products And Raw materials

Raw materials

Preparation Products

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4-Chloro-6-hydroxyquinoline Suppliers

PharmaBlock Sciences (Nanjing),Inc.
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025-86918202 4000255188
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86-025-86918232
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sales@pharmablock.com
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China
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5000
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Shanghai Boc Chemical Co.,Ltd
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021-34975603-808 18721111801
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+86-21-34975602-805
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sales@bocpharma.com
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China
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Nanjing Chemlin Chemical Co., Ltd
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025-83697070
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15883
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Shanghai Hanhong Scientific Co.,Ltd.
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Chengdu Forest Science and Technology Development Co., Ltd.
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18030648795
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1998
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Chiba Pharmaceutical Science and technology Co, Ltd.
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SynAsst Chemical.
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Bide Pharmatech Ltd.
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400-164-7117 13681763483
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+86-21-61629029
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product02@bidepharm.com
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China
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Shanghai Worldyang Chemical Co.,Ltd.
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021-021-56795766
Fax
+86-21-56795266
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sales@worldyachem.com
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China
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Shanghai Xingui Biotechnology Co., Ltd.
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15121041756
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xingui2022@126.com
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China
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9979
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58
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View Lastest Price from 4-Chloro-6-hydroxyquinoline manufacturers

Career Henan Chemical Co
Product
4-Chloro-6-hydroxyquinoline 148018-29-5
Price
US $9.80/KG
Min. Order
1g
Purity
≥99%
Supply Ability
100kg
Release date
2020-01-12