7-Bromoquinolin-3-ol
- Product Name
- 7-Bromoquinolin-3-ol
- CAS No.
- 1261487-70-0
- Chemical Name
- 7-Bromoquinolin-3-ol
- Synonyms
- 7-Bromo-3-quinolinol;7-Bromoquinolin-3-ol;3-Quinolinol, 7-bromo-
- CBNumber
- CB83037690
- Molecular Formula
- C9H6BrNO
- Formula Weight
- 224.05
- MOL File
- 1261487-70-0.mol
7-Bromoquinolin-3-ol Property
- storage temp.
- Sealed in dry,Room Temperature
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye 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
- CD11310698
- Product name
- 7-Bromoquinolin-3-ol
- Purity
- 95+%
- Packaging
- 250mg
- Price
- $359
- Updated
- 2021/12/16
- Product number
- 1261487700
- Product name
- 7-Bromo-3-hydroxyquinoline
- Packaging
- 250mg
- Price
- $488.01
- Updated
- 2021/12/16
- Product number
- CM145548
- Product name
- 7-Bromoquinolin-3-ol
- Purity
- 95%
- Packaging
- 1g
- Price
- $840
- Updated
- 2021/12/16
- Product number
- CD11310698
- Product name
- 7-Bromoquinolin-3-ol
- Purity
- 95+%
- Packaging
- 1g
- Price
- $898
- Updated
- 2021/12/16
- Product number
- 1261487700
- Product name
- 7-Bromo-3-hydroxyquinoline
- Packaging
- 1g
- Price
- $1308.8
- Updated
- 2021/12/16
7-Bromoquinolin-3-ol Chemical Properties,Usage,Production
Synthesis
1246548-95-7
1261487-70-0
General procedure for the synthesis of 7-bromoquinolin-3-ol from 7-bromo-3-methoxyquinoline: 7-bromo-3-methoxyquinoline (1.1 g, 4.62 mmol) was dissolved in acetic acid (20 mL), 48% hydrobromic acid (5.0 mL, 92 mmol) was added, and the reaction was carried out by refluxing the mixture at 120 °C for 4 days. The progress of the reaction was monitored by LCMS, showing a conversion of about 50%. Upon completion of the reaction, the mixture was poured into ice water and the pH was adjusted to alkaline with ammonia. Subsequently, the aqueous phase was extracted with ether (3 x 20 mL), and the organic phases were combined and concentrated. The residue was purified by fast column chromatography (eluent: 10-50% ethyl acetate/hexane) to afford the target product 7-bromoquinolin-3-ol (500 mg, 2.232 mmol, 48% yield) as a tan solid. The product was characterized by 1H NMR (400 MHz, DMSO-d6), chemical shift δ (ppm): 7.55 (d, J=2.53 Hz, 1H), 7.63 (dd, J=8.59,2.02 Hz, 1H), 7.80 (d, J=8.84 Hz, 1H), 8.10 (d, J=1.77 Hz, 1H), 8.60 (d , J=2.78Hz, 1H), 10.51 (s, 1H).
References
[1] Patent: WO2013/52716, 2013, A1. Location in patent: Page/Page column 52
[2] Patent: WO2014/8223, 2014, A2. Location in patent: Page/Page column 74
7-Bromoquinolin-3-ol Preparation Products And Raw materials
Raw materials
Preparation Products
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