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Key Documents

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X600

Sigma-Aldrich

Xanthone

97%

Sinónimos:

9-Xanthenone

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About This Item

Fórmula empírica (notación de Hill):
C13H8O2
Número de CAS:
90-47-1
Peso molecular:
196.20
Beilstein/REAXYS Number:
140443
EC Number:
201-997-7
MDL number:
MFCD00005060
UNSPSC Code:
12352100
PubChem Substance ID:
24902151
NACRES:
NA.22

assay

97%

form

powder

bp

349-350 °C/730 mmHg (lit.)

mp

172-174 °C (lit.)

SMILES string

O=C1c2ccccc2Oc3ccccc13

InChI

1S/C13H8O2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1-8H

InChI key

JNELGWHKGNBSMD-UHFFFAOYSA-N

Gene Information

mouse ... Prkch(18755)

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Categorías relacionadas

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

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Thioxanthone European Pharmacopoeia (EP) Reference Standard

T1305000

Thioxanthone

Rajan Giri et al.
Bioorganic & medicinal chemistry, 18(4), 1456-1463 (2010-02-05)
A series of substituted xanthenes was synthesized and screened for activity using DU-145, MCF-7, and HeLa cancer cell growth inhibition assays. The most potent compound, 9 g ([N,N-diethyl]-9-hydroxy-9-(3-methoxyphenyl)-9H-xanthene-3-carboxamide), was found to inhibit cancer cell growth with IC(50) values ranging from
Ping Wang et al.
Organic letters, 14(3), 902-905 (2012-01-26)
A concise and straightforward strategy to construct a xanthone skeleton via an intramolecular cross-dehydrogenative coupling (CDC) of 2-aryloxybenzaldehydes has been developed. The reaction proceeded smoothly without any need of preactivation of the aldehyde group. It can tolerate various functional groups
Michael A Schätzle et al.
Journal of the American Chemical Society, 134(36), 14742-14745 (2012-08-23)
Reduction of emodin by sodium dithionite resulted in the formation of two tautomeric forms of emodin hydroquinone. Subsequent conversion by the short-chain dehydrogenase/reductase (SDR) MdpC into the corresponding 3-hydroxy-3,4-dihydroanthracen-1(2H)-one implies that deoxygenation is the first step in monodictyphenone biosynthesis. Implications
Jessie A Blake et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 11(3), 539-547 (2012-01-10)
We have attached the antiviral drug acyclovir (ACV) to a xanthone photolabile protecting group (or photocage) through the O6 position of acyclovir, a procedure designed for the treatment of ocular herpes simplex virus infections. Acyclovir is photoreleased from the photocage
Christiane Müller et al.
Journal of the American Chemical Society, 133(41), 16689-16697 (2011-10-01)
Six 2-quinolones, which bear a terminal alkene linked by a three- or four-membered tether to carbon atom C4 of the quinolone, were synthesized and subjected to an intramolecular [2 + 2]-photocycloaddition. The reaction delivered the respective products in high yields
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