376892
2,3-Dimethylanthraquinone
98%
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About This Item
Empirical Formula (Hill Notation):
C16H12O2
CAS Number:
Molecular Weight:
236.27
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
Form:
solid
InChI
1S/C16H12O2/c1-9-7-13-14(8-10(9)2)16(18)12-6-4-3-5-11(12)15(13)17/h3-8H,1-2H3
SMILES string
Cc1cc2C(=O)c3ccccc3C(=O)c2cc1C
InChI key
KIJPZYXCIHZVGP-UHFFFAOYSA-N
assay
98%
form
solid
mp
210-212 °C (lit.)
functional group
ketone
Quality Level
Related Categories
General description
2,3-Dimethylanthraquinone is 2,3-dimethyl substituted anthraquinone and its synthesis has been reported. Electron transfer rate constants for the reaction between radical anions of 2,3-dimethylanthraquinone with benzyl bromide has been evaluated. The photoreactivity of 2,3-dimethylanthraquinone has been evaluated to investigate its usefulness as a photo-reagent for the analysis of ginsenosides using photoreduction fluorescence (PRF) detection method.
Application
2,3-Dimethylanthraquinone may be used as starting reagent in the regioselective synthesis of 6-amino-2,3-anthracenedimethanol.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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2, 3-Dimethylanthraquinone.
Allen CFH and Alan Bell.
Organic Syntheses, 37-37 (1942)
Regioselective syntheses of 5-and 6-aminoanthracene-2, 3-dimethanol.
Sun S and Desper J.
Tetrahedron, 54(3), 411-422 (1998)
Is samarium diiodide an inner-or outer-sphere electron donating agent?
Enem?rke RJ, et al.
Chemical Communications (Cambridge, England), 4, 343-344 (1999)
Photoreactivity of anthraquinones for the analysis of ginsenosides using photoreduction fluorescence detection-HPLC
Park MK, et al.
Archives of Pharmacal Research, 19(6), 562-565 (1996)
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