A89502
蒽黄酸
technical grade, 90%
别名:
2,6-二羟基蒽醌, 蒽黄素
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关于此项目
经验公式（希尔记法）:
C14H8O4
化学文摘社编号:
分子量:
240.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
201-544-3
MDL number:
产品名称
蒽黄酸, technical grade, 90%
InChI
1S/C14H8O4/c15-7-1-3-9-11(5-7)14(18)10-4-2-8(16)6-12(10)13(9)17/h1-6,15-16H
InChI key
APAJFZPFBHMFQR-UHFFFAOYSA-N
SMILES string
Oc1ccc2C(=O)c3cc(O)ccc3C(=O)c2c1
grade
technical grade
assay
90%
form
powder
mp
>320 °C (lit.)
Quality Level
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Application
蒽黄酸可用作合成四羟基四硫富瓦烯(TTF)衍生物的起始材料，在超分子和材料科学中用作氧化还原活性合成砌块。它还还可与乙炔二羧酸二烷基酯和三苯基膦反应，用于制备膦亚基蒽[2,1-b]呋喃。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
A Rodriguez et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 75(1), 479-485 (2009-12-08)
Semiconducting molecular-material thin-films of tetrabenzo (b,f,j,n) [1,5,9,13] tetraazacyclohexadecine copper(II) and nickel(II) bisanthraflavates have been prepared by using vacuum thermal evaporation on Corning glass substrates and crystalline silicon wafers. The films thus obtained were characterized by infrared spectroscopy (FTIR), atomic force
A D Ayrton et al.
Mutation research, 207(3-4), 121-125 (1988-03-01)
The ability of anthraflavic acid to inhibit the mutagenicity of IQ was investigated using the Ames test and employing hepatic activation systems from Aroclor 1254-pretreated rats. Incorporation of anthraflavic acid into the S9 mix caused a concentration-dependent decrease in the
Jie Liu et al.
Nature communications, 6, 10032-10032 (2015-12-02)
The integration of high charge carrier mobility and high luminescence in an organic semiconductor is challenging. However, there is need of such materials for organic light-emitting transistors and organic electrically pumped lasers. Here we show a novel organic semiconductor, 2,6-diphenylanthracene
Extrapolation of in vitro antimutagenicity to the in vivo situation: the case for anthraflavic acid.
C Ioannides et al.
Basic life sciences, 61, 103-110 (1993-01-01)
H Mukhtar et al.
Cancer research, 48(9), 2361-2365 (1988-05-01)
Our recent studies have shown that naturally occurring dietary plant phenols such as tannic acid, quercetin, myricetin, and anthraflavic acid are capable of inhibiting polycyclic aromatic hydrocarbon (PAH) metabolism and subsequent PAH-DNA adduct formation in epidermis of SENCAR mice (M.
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