CasNo.2213-63-0,2213-63-0 2,3-Dichloroquinoxaline Factory in China CAS NO.2213-63-0,(2213-63-0) Suppliers

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2213-63-0 2,3-Dichloroquinoxaline Factory in China CAS NO.2213-63-0 C8H4Cl2N2

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Tech Data Relevant

1.Certificate Of Analysis (COA)

2..Material Safety Data Sheet (MSDS)

3.Technical Data Sheet(TDS)

4.Route of synthesis (ROS)

5.Nuclear Magnetic Resonance(NMR)

6.Method of Analysis(MOA)

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2213-63-0

2,3-Dichloroquinoxaline

PRODUCT INFORMATION :

2,3-Dichloroquinoxaline Basic information

Product Name:	2,3-Dichloroquinoxaline
Synonyms:	2,3-dichloro-quinoxalin;cp42103-4;AKOS BBS-00006726;2,3-DICHLOROQUINOXALINE;SALOR-INT L497169-1EA;TIMTEC-BB SBB003555;2,3-Dichloroquinoxaline,96%;Quinoxaline, 2,3-dichloro.
CAS:	2213-63-0
MF:	C8H4Cl2N2
MW:	199.04
EINECS:	218-667-3
Product Categories:	Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;Quinoxalines;QuinoxalinesHeterocyclic Building Blocks
Mol File:	2213-63-0.mol

2,3-Dichloroquinoxaline Chemical Properties

mp	152-154 °C(lit.)
BRN	126076
Stability:	Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference	2213-63-0(CAS DataBase Reference)
EPA Substance Registry System	Quinoxaline, 2,3-dichloro-(2213-63-0)

Safety Information

Hazard Codes	T
Risk Statements	25-36/37/38
Safety Statements	26-36/37/39-45-37/39-28A
RIDADR	2811
WGK Germany	3
RTECS	VD1720000
HazardClass	6.1
PackingGroup	III

MSDS Information

Provider	Language
2,3-Dichloroquinoxaline	English
SigmaAldrich	English
ACROS	English
ALFA	English

2,3-Dichloroquinoxaline Usage And Synthesis

Chemical Properties	solid
Usage	2,3-Dichloroquinoxaline is a dichlorinated quinoxaline derivative with antimicrobial activity. 2,3-Dichloroquinoxaline is used in the preparation of quinoxaline derivatives of cancer chemopreventive a ctivity.
General Description	Gray solid. Insoluble in water.
Air & Water Reactions	Insoluble in water.
Reactivity Profile	A halogenated amine. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides.
Fire Hazard	2,3-Dichloroquinoxaline is probably combustible.