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6-(bromomethyl)quinoxaline

Product Name
6-(bromomethyl)quinoxaline
CAS No.
53967-21-8
Chemical Name
6-(bromomethyl)quinoxaline
Synonyms
6-(bromomethyl)quinoxaline;Quinoxaline, 6-(bromomethyl)-
CBNumber
CB31515812
Molecular Formula
C9H7BrN2
Formula Weight
223.07
MOL File
53967-21-8.mol
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6-(bromomethyl)quinoxaline Property

Boiling point:
325.7±27.0 °C(Predicted)
Density 
1.599±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
0.52±0.30(Predicted)
Appearance
Yellow to brown Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H302Harmful if swallowed

H314Causes severe skin burns and eye damage

Precautionary statements

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

P280Wear protective gloves/protective clothing/eye protection/face protection.

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

P310Immediately call a POISON CENTER or doctor/physician.

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N-Bromosuccinimide Price

Biosynth Carbosynth
Product number
FB144127
Product name
6-(Bromomethyl)quinoxaline
Packaging
100mg
Price
$72
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB144127
Product name
6-(Bromomethyl)quinoxaline
Packaging
250mg
Price
$145
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB144127
Product name
6-(Bromomethyl)quinoxaline
Packaging
500mg
Price
$250
Updated
2021/12/16
Biosynth Carbosynth
Product number
FB144127
Product name
6-(Bromomethyl)quinoxaline
Packaging
1g
Price
$437
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0367840
Product name
6-(BROMOMETHYL)QUINOXALINE
Purity
95.00%
Packaging
5MG
Price
$498.69
Updated
2021/12/16
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6-(bromomethyl)quinoxaline Chemical Properties,Usage,Production

Synthesis

6344-72-5

53967-21-8

General procedure for the synthesis of 6-bromomethylquinoxaline from 6-methylquinoxaline: a mixture of 6-methylquinoxaline (2.0 g, 13.9 mmol), N-bromosuccinimide (3.0 g, 16.9 mmol), and benzoyl peroxide (411 mg, 1.7 mmol) in anhydrous carbon tetrachloride (50 mL) was subjected to stirring and reacted for 48 hours under reflux conditions . Upon completion of the reaction, the mixture was cooled to room temperature and diluted with the addition of dichloromethane (50 mL). Subsequently, the reaction mixture was washed sequentially with 1N sodium hydroxide solution (1 x 100 mL) and saturated saline (1 x 100 mL). The organic phase was separated, dried with anhydrous magnesium sulfate, filtered and the solvent was concentrated under reduced pressure to give the crude product. Finally, the crude product was purified by fast column chromatography (eluent: 0-30% ethyl acetate/hexane gradient elution) to afford the target compound 6-bromomethylquinoxaline (1.10 g, 35% yield).

References

[1] ChemMedChem, 2017, vol. 12, # 3, p. 257 - 270
[2] Journal of Medicinal Chemistry, 1995, vol. 38, # 4, p. 617 - 628
[3] Patent: WO2010/132999, 2010, A1. Location in patent: Page/Page column 111
[4] Patent: WO2011/23753, 2011, A1. Location in patent: Page/Page column 74-75

6-(bromomethyl)quinoxaline Preparation Products And Raw materials

Raw materials

Preparation Products

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6-(bromomethyl)quinoxaline Suppliers

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