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X600

Xanthone

Name: Xanthone
Brand: ALDRICH

97%

Synonym(s):

9-Xanthenone

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About This Item

Empirical Formula (Hill Notation):

C₁₃H₈O₂

CAS Number:

90-47-1

Molecular Weight:

196.20

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24902151

EC Number:

201-997-7

Beilstein/REAXYS Number:

140443

MDL number:

MFCD00005060

Assay:

97%

Form:

powder

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Properties

Quality Level

100

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)

Description

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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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Synthesis and cancer cell cytotoxicity of substituted xanthenes.

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

Benzophenones and xanthones from Garcinia cantleyana var. cantleyana and their inhibitory activities on human low-density lipoprotein oxidation and platelet aggregation.

Ibrahim Jantan et al.

Phytochemistry, 80, 58-63 (2012-05-30)

Three benzophenones, 2,6,3',5'-tetrahydroxybenzophenone (1), 3,4,5,3',5'-pentahydroxybenzophenone (3) and 3,5,3',5'-tetrahydroxy-4-methoxybenzophenone (4), as well as a xanthone, 1,3,6-trihydroxy-5-methoxy-7-(3'-methyl-2'-oxo-but-3'-enyl)xanthone (9), were isolated from the twigs of Garcinia cantleyana var. cantleyana. Eight known compounds, 3,4,5,3'-tetrahydroxy benzophenone (2), 1,3,5-trihydroxyxanthone (5), 1,3,8-trihydroxyxanthone (6), 2,4,7-trihydroxyxanthone (7), 1,3,5,7-tetrahydroxyxanthone (8)

Copper(I)-catalyzed intramolecular O-arylation for the synthesis of 2,3,4,9-tetrahydro-1H-xanthen-1-ones with low loads of CuCl.

Kavitha Sudheendran et al.

The Journal of organic chemistry, 77(22), 10194-10210 (2012-10-17)

As little as 0.5 mol % CuCl is sufficient to catalyze the intramolecular O-arylation of easily accessible 2-(2-bromobenzyl)cyclohexane-1,3-diones to provide the corresponding 2,3,4,9-tetrahydro-1H-xanthen-1-ones with yields ranging from 83% to 99%.

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Global Trade Item Number

SKU	GTIN
X600-25G	04061837549809