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Quinoxaline, 6-(chloromethyl)-

Product Name
Quinoxaline, 6-(chloromethyl)-
CAS No.
477776-17-3
Chemical Name
Quinoxaline, 6-(chloromethyl)-
Synonyms
6-(Chloromethyl)quinoxaline;Quinoxaline, 6-(chloromethyl)-
CBNumber
CB61860320
Molecular Formula
C9H7ClN2
Formula Weight
0
MOL File
477776-17-3.mol
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Quinoxaline, 6-(chloromethyl)- Property

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
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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

H332Harmful if inhaled

H335May cause respiratory irritation

Precautionary statements

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

Ambeed
Product number
A142308
Product name
6-(Chloromethyl)quinoxaline
Purity
95+%
Packaging
100mg
Price
$94
Updated
2021/12/16
Ambeed
Product number
A142308
Product name
6-(Chloromethyl)quinoxaline
Purity
95+%
Packaging
250mg
Price
$187
Updated
2021/12/16
Crysdot
Product number
CD11118864
Product name
6-(Chloromethyl)quinoxaline
Purity
95+%
Packaging
250mg
Price
$277
Updated
2021/12/16
Crysdot
Product number
CD11118864
Product name
6-(Chloromethyl)quinoxaline
Purity
95+%
Packaging
1g
Price
$554
Updated
2021/12/16
Alichem
Product number
477776173
Product name
6-(Chloromethyl)quinoxaline
Packaging
1g
Price
$896.66
Updated
2021/12/16
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Quinoxaline, 6-(chloromethyl)- Chemical Properties,Usage,Production

Synthesis

6344-72-5

477776-17-3

The general procedure for the synthesis of 6-(chloromethyl)quinoxaline from 6-methylquinoxaline is as follows: Example 1: Catalytic air dehydrogenation of 6-hydroxymethyl-methyl-quinoxaline In a 500 mL round-bottomed flask, 6-methylquinoxaline (10 g, 69.4 mmol) was dissolved in 240 g of acetonitrile with N-chlorosuccinimide (14 g, 105.3 mmol). Benzoyl peroxide (0.4 g, 1.65 mmol) was added as initiator. A reflux condenser was installed and the reaction mixture was heated and refluxed for 6 hours, followed by the addition of benzoyl peroxide (0.1 g). The reflux reaction was continued for a total reaction time of 12 hours. Upon completion of the reaction, the reaction solution was analyzed by gas chromatography (GC), which showed the generation of 6-(chloromethyl)quinoxaline with 80% selectivity and 60% conversion.

References

[1] Patent: US6559308, 2003, B1

Quinoxaline, 6-(chloromethyl)- Preparation Products And Raw materials

Raw materials

Preparation Products

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Quinoxaline, 6-(chloromethyl)- Suppliers

Aikon International Limited
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China
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Energy Chemical
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Jilin Chinese Academy of Sciences-yanshen Technology
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Synthonix Inc
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United States
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477776-17-3, Quinoxaline, 6-(chloromethyl)-Related Search:


  • Quinoxaline, 6-(chloromethyl)-
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