ChemicalBook > CAS DataBase List > 6-Bromoquinolin-4(1H)-one

6-Bromoquinolin-4(1H)-one

Product Name
6-Bromoquinolin-4(1H)-one
CAS No.
332366-57-1
Chemical Name
6-Bromoquinolin-4(1H)-one
Synonyms
6-Bromoquinolin-4(1H);6-BroMo-1H-quinolin-4-one;6-Bromoquinolin-4(1H)-one;6-Bromo-4(1H)-quinolinone;4(1H)-Quinolinone, 6-bromo-;6-BROMO-1,4-DIHYDROQUINOLIN-4-ONE
CBNumber
CB72504330
Molecular Formula
C9H6BrNO
Formula Weight
224.05
MOL File
332366-57-1.mol
More
Less

6-Bromoquinolin-4(1H)-one Property

Melting point:
282-284 °C
Boiling point:
321.7±42.0 °C(Predicted)
Density 
1.620±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
1.39±0.50(Predicted)
Appearance
Off-white to light yellow Solid
More
Less

Hazard and Precautionary Statements (GHS)

More
Less

N-Bromosuccinimide Price

TRC
Product number
B807888
Product name
6-Bromoquinolin-4(1H)-one
Packaging
1g
Price
$60
Updated
2021/12/16
AK Scientific
Product number
3851AB
Product name
6-Bromoquinolin-4(1H)-one
Packaging
1g
Price
$107
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0060987
Product name
6-BROMO-1,4-DIHYDROQUINOLIN-4-ONE
Purity
95.00%
Packaging
1G
Price
$852.55
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0060987
Product name
6-BROMO-1,4-DIHYDROQUINOLIN-4-ONE
Purity
95.00%
Packaging
2.5G
Price
$1227.82
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0060987
Product name
6-BROMO-1,4-DIHYDROQUINOLIN-4-ONE
Purity
95.00%
Packaging
5G
Price
$1548.26
Updated
2021/12/16
More
Less

6-Bromoquinolin-4(1H)-one Chemical Properties,Usage,Production

Uses

6-Bromoquinolin-4(1H)-one is a reagent used for the enantioselective prepartion of tetrahydroquinolinones and dihydro- and tetrahydropyridinones by copper-catalyzed addn. of Grignard reagents to quinolinones and pyridones

Synthesis

187278-01-9

145369-94-4

General procedure for the synthesis of 6-bromo-4-hydroxyquinoline from 5-[(4-bromophenylamino)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione: First, Meldrum acid (1) (32.4 g, 225.0 mmol) was dissolved in trimethyl orthoformate (250 mL), stirred and heated to reflux for 3 h under nitrogen protection to obtain Intermediate 2. After the solution was cooled to about 50 °C, a solution of 4-bromoaniline (25.8 g, 150.0 mmol) in trimethyl orthoformate (80 mL) was slowly added dropwise. After the dropwise addition was completed, the reaction mixture was continued to be heated and refluxed for 2 hours. Upon completion of the reaction, the solvent was evaporated under reduced pressure, the residue was diluted with hexane, filtered, and the solid portion was washed with hexane and dried to afford the yellow solid Meldrum's acid derivative 3. Subsequently, compound 3 was slowly added in portions (~1.0 g each) to diphenyl ether (Ph2O, 500 mL) preheated to 245°C. The rate of addition needs to be carefully controlled to prevent violent gas release. The reaction mixture was heated at 250 °C with stirring for 15 min, then cooled to room temperature, diluted with hexane and filtered. The solids were washed sequentially with hexane and 30% ether/hexane mixture. The crude product was purified by silica gel column chromatography (eluent ratio 16:1 to 10:1 dichloromethane/methanol), resulting in a light brown solid 6-bromo-4-hydroxyquinoline (4) (24.6 g, 73% yield) with a melting point of 282-284 °C (literature value 282-284 °C). Its 1H NMR (DMSO-d6) data were as follows: δ 11.93 (broad single peak, 1H, NH), 8.17 (double peak, J=2.0 Hz, 1H, Ar-H), 7.96 (double double peak, J=7.5,6.0 Hz, 1H), 7.79 (double double peak, J=9.0,2.5 Hz, 1H, Ar-H), 7.53 (double peak, J= 8.5 Hz, 1H), 6.08 (double peak, J=2.5 Hz, 1H, Ar-H).

References

[1] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 4, p. 1569 - 1574
[2] Tetrahedron, 2001, vol. 57, # 6, p. 1005 - 1013
[3] Advanced Synthesis and Catalysis, 2010, vol. 352, # 14-15, p. 2445 - 2449
[4] Patent: EP2913330, 2015, A1. Location in patent: Paragraph 0583
[5] Patent: CN106432073, 2017, A. Location in patent: Paragraph 0050; 0051; 0054; 0055

6-Bromoquinolin-4(1H)-one Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

6-Bromoquinolin-4(1H)-one Suppliers

Shanghai Sunway Pharmaceutical Technology Co., Ltd
Tel
18270980682
Fax
021 51613951
Email
mlcheng@sunwaypharm.cn
Country
China
ProdList
8669
Advantage
57
SuZhou ShiYa Biopharmaceuticals, Inc.
Tel
86(512)5235 8471 17715136450
Fax
86(512)5235 6881
Email
sales@shiyabiopharm.com
Country
China
ProdList
4169
Advantage
58
Shanghai Carlow Chemicals Co., Ltd.
Tel
21-33526724 18930996265
Fax
37023730
Email
info@carlowchem.com
Country
China
ProdList
1922
Advantage
58
JW & Y Pharmlab Co., Ltd.
Tel
021-64340559 13651849907;
Fax
021- 64345308
Email
xinyu_shi@jwypharmlab.com.cn
Country
China
ProdList
12000
Advantage
58
Shanghai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847; 18021002903
Fax
QQ:3008007432
Email
3008007409@qq.com
Country
China
ProdList
71826
Advantage
60
ChengDu TongChuangYuan Pharmaceutical Co.Ltd
Tel
028-83379370 13880556291
Fax
028-87747383
Email
tcy@tcypharm.com
Country
China
ProdList
7218
Advantage
58
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131957
Advantage
58
Chongqing Chemieliva Pharmaceutical Co., Ltd.
Tel
18696571988
Fax
+86 (23) 6777-0220
Email
amy.lei@chemieliva.com
Country
China
ProdList
1554
Advantage
60
Zhengzhou Huiju Chemical Co., Ltd.
Tel
0371-55900031 18137872243
Fax
QQ:2853979815
Email
2853979815@qq.com
Country
China
ProdList
9996
Advantage
55
Aikon International Limited
Tel
025-66061636 18013972705
Fax
(3)02557626880
Email
qqyang@aikonchem.com
Country
China
ProdList
15814
Advantage
58
More
Less

View Lastest Price from 6-Bromoquinolin-4(1H)-one manufacturers

Career Henan Chemical Co
Product
6-Bromoquinolin-4(1H)-one 332366-57-1
Price
US $1.00/KG
Min. Order
1KG
Purity
97%
Supply Ability
200KG
Release date
2018-08-15

332366-57-1, 6-Bromoquinolin-4(1H)-oneRelated Search:


  • 6-Bromoquinolin-4(1H)-one
  • 6-BroMo-1H-quinolin-4-one
  • 6-BROMO-1,4-DIHYDROQUINOLIN-4-ONE
  • 6-Bromoquinolin-4(1H)
  • 6-Bromo-4(1H)-quinolinone
  • 4(1H)-Quinolinone, 6-bromo-
  • 332366-57-1