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
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
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.
N-Bromosuccinimide Price
- Product number
- HCH0367832
- Product name
- 6-BROMOISOQUINOLIN-4-OL
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $504.52
- Updated
- 2021/12/16
- Product number
- CD11366814
- Product name
- 6-Bromoisoquinolin-4-ol
- Purity
- 95+%
- Packaging
- 1g
- Price
- $588
- Updated
- 2021/12/16
- Product number
- UT01926
- Product name
- 6-Bromoisoquinolin-4-ol
- Purity
- 97%
- Packaging
- 0.5g
- Price
- $600
- Updated
- 2021/12/16
- Product number
- 1015070560
- Product name
- 6-Bromoisoquinolin-4-ol
- Packaging
- 1g
- Price
- $669.5
- Updated
- 2021/12/16
- Product number
- CM145038
- Product name
- 6-bromoisoquinolin-4-ol
- Purity
- 95%
- Packaging
- 1g
- Price
- $729
- Updated
- 2021/12/16
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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