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MilliporeSigma

X201

Xanthene

99%

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About This Item

Empirical Formula (Hill Notation):
C13H10O
CAS Number:
92-83-1
Molecular Weight:
182.22
EC Number:
202-194-4
UNSPSC Code:
12352100
PubChem Substance ID:
24902135
Beilstein/REAXYS Number:
133939
MDL number:
MFCD00005055
Assay:
99%

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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.)

mp

101-102 °C (lit.)

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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.[1]

Application

Xanthene can be used as:
  • A reactant in the dehydrogenative cross-coupling reaction with carbonyl compounds.[2][3]
  • A substrate to synthesize N-xanthyl-p-toluenesulfonamide via C−H amination with tosyl azide using rhodium catalyst.[4]

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H317

pcodes

P280

Hazard Classifications

Skin Sens. 1

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, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBJ4251V
02014CJ
03003MP
00822CX
04511DW

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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
Electrochemical dehydrogenative cross-coupling of xanthenes with ketones
Yang Y-Z, et al.
Chemical Communications (Cambridge, England), 56(14), 7585-7588 (2020)
Evgeniy Dukhopelnykov et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 247, 119114-119114 (2020-11-10)
The interaction between xanthene dye eosin Y and double stranded DNA has been studied by spectrophotometry. The conventional titration study does not show the interaction in the eosin Y - DNA system. Therefore, the competitive binding assay was carried out.
Nguyen Khoa Hien et al.
ACS omega, 5(33), 21241-21249 (2020-09-03)
A novel coumarin derivative (5) was synthesized and used as a colorimetric and fluorescent probe for selective detection of Cu2+ ions in the presence of other metal ions, with the detection limits of 5.7 and 4.0 ppb, respectively. Cu2+ ion
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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