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6-BroMoisoquinolin-4-ol

Product Name
6-BroMoisoquinolin-4-ol
CAS No.
1015070-56-0
Chemical Name
6-BroMoisoquinolin-4-ol
Synonyms
6-BroMoisoquinolin-4-ol;4-Isoquinolinol, 6-bromo-
CBNumber
CB72732595
Molecular Formula
C9H6BrNO
Formula Weight
224.05
MOL File
1015070-56-0.mol
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6-BroMoisoquinolin-4-ol Property

Boiling point:
476.4±25.0 °C(Predicted)
Density 
1.705±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
4.79±0.40(Predicted)
Appearance
Light brown to brown Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
HCH0367832
Product name
6-BROMOISOQUINOLIN-4-OL
Purity
95.00%
Packaging
5MG
Price
$504.52
Updated
2021/12/16
Crysdot
Product number
CD11366814
Product name
6-Bromoisoquinolin-4-ol
Purity
95+%
Packaging
1g
Price
$588
Updated
2021/12/16
Acrotein
Product number
UT01926
Product name
6-Bromoisoquinolin-4-ol
Purity
97%
Packaging
0.5g
Price
$600
Updated
2021/12/16
Alichem
Product number
1015070560
Product name
6-Bromoisoquinolin-4-ol
Packaging
1g
Price
$669.5
Updated
2021/12/16
Chemenu
Product number
CM145038
Product name
6-bromoisoquinolin-4-ol
Purity
95%
Packaging
1g
Price
$729
Updated
2021/12/16
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6-BroMoisoquinolin-4-ol Chemical Properties,Usage,Production

Synthesis

1235382-79-2

1015070-56-0

General procedure for the synthesis of 6-bromo-4-hydroxyisoquinoline from the compound (CAS: 1235382-79-2): 6-bromo-2-(phenylsulfonyl)-2,3-dihydroisoquinolin-4(1H)-one was first prepared from 4-bromobenzyl bromide with reference to the method reported in Tetrahedron 61 (2005) 8282 (29 g, 79.2 mmol ). The product was then suspended in ethanol (300 mL). To this suspension was added 21% sodium ethoxide/ethanol solution (88.6 mL, 238 mmol) and the reaction was stirred for 1 hour at room temperature. Upon completion of the reaction, 5 M hydrochloric acid (~50 mL) was added to the reaction solution for neutralization, followed by removal of ethanol by distillation under reduced pressure. The precipitated solid precipitate was collected by filtration. The resulting solid was dried and purified by silica gel column chromatography (eluent: dichloromethane/methanol, gradient from 100:0 to 50:50, v/v), resulting in the target product 6-bromo-4-hydroxyisoquinoline (13.2 g, 75% yield).1H-NMR (DMSO-d6) δ: 7.79 (1H, dd, J = 8.7, 1.8 Hz),. 8.03 (1H, d, J = 8.7 Hz), 8.11 (1H, s), 8.25-8.27 (1H, m), 8.82 (1H, s), 10.62 (1H, s).

References

[1] Patent: EP2380878, 2011, A1. Location in patent: Page/Page column 30

6-BroMoisoquinolin-4-ol Preparation Products And Raw materials

Raw materials

Preparation Products

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6-BroMoisoquinolin-4-ol Suppliers

Chengdu Forest Science and Technology Development Co., Ltd.
Tel
18030648795
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028-61777050
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sales@cdforestchem.com
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China
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Nantong MYBio-pharm. Co., Ltd.
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ShangHai AmK Pharmaceutical Technology Co., Ltd.
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Amadis Chemical Company Limited
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Cochemical Ltd.
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Aikon International Limited
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Shanghai Jizhi Biochemical Technology Co. Ltd.
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Nantong puyue biomedical Co., Ltd
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1015070-56-0, 6-BroMoisoquinolin-4-olRelated Search:


  • 6-BroMoisoquinolin-4-ol
  • 4-Isoquinolinol, 6-bromo-
  • 1015070-56-0