ChemicalBook > CAS DataBase List > 7-Bromoquinolin-3-ol

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
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7-Bromoquinolin-3-ol Property

storage temp. 
Sealed in dry,Room Temperature
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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

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

Crysdot
Product number
CD11310698
Product name
7-Bromoquinolin-3-ol
Purity
95+%
Packaging
250mg
Price
$359
Updated
2021/12/16
Alichem
Product number
1261487700
Product name
7-Bromo-3-hydroxyquinoline
Packaging
250mg
Price
$488.01
Updated
2021/12/16
Chemenu
Product number
CM145548
Product name
7-Bromoquinolin-3-ol
Purity
95%
Packaging
1g
Price
$840
Updated
2021/12/16
Crysdot
Product number
CD11310698
Product name
7-Bromoquinolin-3-ol
Purity
95+%
Packaging
1g
Price
$898
Updated
2021/12/16
Alichem
Product number
1261487700
Product name
7-Bromo-3-hydroxyquinoline
Packaging
1g
Price
$1308.8
Updated
2021/12/16
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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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