Skip to Content
Merck
All Photos(1)

Key Documents

144789

Sigma-Aldrich

2,3-Dihydroxyquinoxaline

98%

Synonym(s):

2,3(1H,4H)-Quinoxalinedione, 2,3-Quinoxalinediol

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C8H6N2O2
CAS Number:
Molecular Weight:
162.15
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

solid

mp

>300 °C (lit.)

SMILES string

Oc1nc2ccccc2nc1O

InChI

1S/C8H6N2O2/c11-7-8(12)10-6-4-2-1-3-5(6)9-7/h1-4H,(H,9,11)(H,10,12)

InChI key

ABJFBJGGLJVMAQ-UHFFFAOYSA-N

Gene Information

Looking for similar products? Visit Product Comparison Guide

General description

2,3-Dihydroxyquinoxaline(dhq) undergoes electrophilic substitution reaction with sulphuric acid solution and potassium nitrate to form 2,3-dihydroxy-6-nitroquinoxaline. It reacts with Ru3(CO)12 in DMSO to give the Ru(CO)2(dhq)(DMSO) complex.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Ruthenium, osmium and rhodium-2, 3-bis (2'-pyridyl) quinoxaline complexes.
Abdel-Shafi AA, et al.
Transition Met. Chem. (London), 27(1), 69-74 (2002)
The measurement of urinary oxalic acid by derivatization coupled with liquid chromatography.
J F Murray et al.
Analytical biochemistry, 121(2), 301-309 (1982-04-01)
223. Quinoxalines and related compounds. Part VI. Substitution of 2, 3-dihydroxyquinoxaline and its 1, 4-dimethyl derivative.
Cheeseman GWH.
Journal of the Chemical Society, 27(1), 1170-1176 (1962)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service