InChI key
RZVHIXYEVGDQDX-UHFFFAOYSA-N
InChI
1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H
SMILES string
O=C1c2ccccc2C(=O)c3ccccc13
grade
analytical standard
vapor density
7.16 (vs air)
vapor pressure
1 mmHg ( 190 °C)
packaging
ampule of 1 g
manufacturer/tradename
Chem Service, Inc. PS-926
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
379-381 °C (lit.)
mp
284-286 °C (lit.)
format
neat
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Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
signalword
Danger
hcodes
Hazard Classifications
Carc. 1B - Skin Sens. 1
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
flash_point_f
482.0 °F - closed cup
flash_point_c
250 °C - closed cup
Leila Qasemian et al.
Chemosphere, 84(10), 1321-1328 (2011-06-15)
Mediterranean coastal ecosystems are known to be highly subject to natural and anthropic environmental stress. In this study, we examine the effects of anthracene as a common pollutant on the total microbial communities from a Pinus halepensis litter of a
A A Stepanov et al.
The Journal of organic chemistry, 76(21), 8737-8748 (2011-09-14)
The nature of products in the diazotization of 1-amino-2-acetylenyl-9,10-anthraquinones strongly depends on the nature of substituents at both the alkyne and at the anthraquinone core. Donor substitution (NHAr, OH) at the fourth position stabilizes the diazonium salt at C1, decelerating
Witold Nowik et al.
Journal of chromatography. A, 1218(23), 3636-3647 (2011-05-03)
A series of reversed phases bonded with several functional groups was investigated for separation of anthraquinone derivatives, following the previous work, dedicated to the selectivity of octadecyl silica bonded phases. Considering wide diversity of substitutions in hydrophobic anthraquinone skeleton, interactions
Gui'e Xie et al.
British journal of pharmacology, 159(3), 689-697 (2010-02-05)
The aims of this study were to investigate the anti-cancer activity of SZ-685C, an anthracycline analogue isolated from marine-derived mangrove endophytic fungi, and to explore the molecular mechanisms underlying such activity. The effect of SZ-685C on the viability of cancer
Myriam Bonose-Crosnier de Bellaistre et al.
Journal of chromatography. A, 1218(6), 778-786 (2011-01-14)
Chromatographic study of natural products helps to determine their molecular composition and to identify their sources (biological, geographical, etc.). However, identifying anthraquinoids is still a challenge because this chemical family is composed of more than half a thousand molecules. In
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