X201
Xanthene
99%
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About This Item
Empirical Formula (Hill Notation):
C13H10O
CAS Number:
Molecular Weight:
182.22
EC Number:
202-194-4
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
133939
MDL number:
Assay:
99%
InChI key
GJCOSYZMQJWQCA-UHFFFAOYSA-N
InChI
1S/C13H10O/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12/h1-8H,9H2
SMILES string
C1c2ccccc2Oc3ccccc13
assay
99%
bp
310-312 °C (lit.)
General description
Xanthene (10H-9-oxaanthracene) is a heterocyclic compound generally used as an important building block in organic synthesis. It is a core moiety of many dyes like fluorescein, eosins, and rhodamines.
Application
Xanthene can be used as:
- A reactant in the dehydrogenative cross-coupling reaction with carbonyl compounds.
- A substrate to synthesize N-xanthyl-p-toluenesulfonamide via C−H amination with tosyl azide using rhodium catalyst.
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Meng Chen et al.
Journal of chromatography. A, 1590, 27-38 (2019-01-12)
An analytical methodology for comprehensive screening of 63 coloring agents of great concern for regulatory control in cosmetics has been established using ultra-high-performance liquid chromatography (UHPLC) coupled with quadrupole-Orbitrap high-resolution mass spectrometry (Q-Orbitrap HRMS). An effective, rapid, and simple sample
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Electrochemical dehydrogenative cross-coupling of xanthenes with ketones
Yang Y-Z, et al.
Chemical Communications (Cambridge, England), 56(14), 7585-7588 (2020)
Yita Wang et al.
Nanomaterials (Basel, Switzerland), 8(7) (2018-07-07)
The electro-Fenton (EF) process is a type of electrochemical oxidation process; ·OH radicals are generated on the cathode using electricity and decolorize dye wastewaters. Most studies on EF systems in the past have focused on the operating parameters of this
Catalytic C-H amination driven by intramolecular ligand-to-nitrene one-electron transfer through a rhodium (III) centre
Fujita D, et al.
Chemical Communications (Cambridge, England), 53(35), 4849-4852 (2017)
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