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136301

Sigma-Aldrich

2-Chloroquinoxaline

98%

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About This Item

Empirical Formula (Hill Notation):
C8H5ClN2
CAS Number:
Molecular Weight:
164.59
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

bp

100 °C/1.4 mmHg (lit.)

mp

47-50 °C (lit.)

functional group

chloro

SMILES string

Clc1cnc2ccccc2n1

InChI

1S/C8H5ClN2/c9-8-5-10-6-3-1-2-4-7(6)11-8/h1-5H

InChI key

BYHVGQHIAFURIL-UHFFFAOYSA-N

Application

2-Chloroquinoxaline (QCI) was used to study the effect of solvent on hydrolysis of QCI in aqueous–organic solvent mixtures with acetonitrile and dimethylesulphoxide. It was used in the synthesis of 2-(3-butynyl-2-methyl-2-ol) quinoxaline.It was used as reagent in the synthesis of chloroquinoxaline sulfamide.

Pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


Certificates of Analysis (COA)

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Kelly G Matz et al.
Inorganic chemistry, 50(20), 9804-9815 (2011-09-08)
A model system for the molybdenum cofactor has been developed that illustrates the noninnocent behavior of an N-heterocycle appended to a dithiolene chelate on molybdenum. The pyranopterin of the molybdenum cofactor is modeled by a quinoxalyldithiolene ligand (S(2)BMOQO) formed from
Kinetics of the Reaction of 2-Chloro-quinoxaline with Hydroxide Ion in ACN-H2O and DMSO-H2O Binary Solvent Mixtures.
Fathalla MF.
Journal of Solution Chemistry, 40(7), 1258-1270 (2011)

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