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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
Molecular Weight:
0
MDL Number:
MFCD15144408
MOL File:
477776-17-3.mol
Last updated:2026-05-28 02:19:43

Quinoxaline, 6-(chloromethyl)- Properties

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

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H332-H335
Precautionary statements  P280-P305+P351+P338-P310

Quinoxaline, 6-(chloromethyl)- price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Activate Scientific AS115660 6-(Chloromethyl)quinoxaline 97% 477776-17-3 1g $916 2026-06-04 Buy
Synthonix C51081 6-(Chloromethyl)quinoxaline 95+% 477776-17-3 100mg $300 2026-05-06 Buy
Synthonix C51081 6-(Chloromethyl)quinoxaline 95+% 477776-17-3 250mg $360 2026-05-06 Buy
Synthonix C51081 6-(Chloromethyl)quinoxaline 95+% 477776-17-3 1g $710 2026-05-06 Buy
Synthonix C51081 6-(Chloromethyl)quinoxaline 95+% 477776-17-3 5g $2000 2026-05-06 Buy
Product number Packaging Price Buy
AS115660 1g $916 Buy
C51081 100mg $300 Buy
C51081 250mg $360 Buy
C51081 1g $710 Buy
C51081 5g $2000 Buy

Quinoxaline, 6-(chloromethyl)- Chemical Properties,Uses,Production

Synthesis

6-Methylquinoxaline

6344-72-5

Quinoxaline,  6-(chloromethyl)-

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

Quinoxaline, 6-(chloromethyl)- Suppliers

Global( 12)Suppliers
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Aikon International Limited 025-66113011 19370895928 qzhang@aikonchem.com China 15390 58
Suzhou Nuoouman Biological Technology Co., Ltd. 15026866316 180642609@qq.com China 4969 58
Energy Chemical 021-58432009 400-005-6266 marketing@energy-chemical.com China 44871 58
Shanghai Sunway Pharmaceutical Technology Co.,Ltd. 13611835272 13611835272 mmwang@sunwaypharm.com China 44090 58
Hubei Co-prosperity Medicine Technonlogy Co., Ltd 2383948258 19172820304 2383948258@qq.com China 12983 58
Hefei Mokai Pharmaceutical Technology Co., Ltd 18130062233 690231469@qq.com China 8000 58
Biokitchen 021-021-021-31663258 13795219287 donghuanwen@126.com China 3077 58
Shanghai Kangenbo Medical Technology Co., Ltd. 17510465506 renhuirong@kangenbo.cn China 9998 58
Jilin Chinese Academy of Sciences-yanshen Technology 18143011203 info@chemextension.com China 42052 58
Quinoxaline, 6-(chloromethyl)- 6-(Chloromethyl)quinoxaline 477776-17-3