推荐产品
等級
technical grade
品質等級
化驗
90%
形狀
powder
mp
>320 °C (lit.)
SMILES 字串
Oc1ccc2C(=O)c3cc(O)ccc3C(=O)c2c1
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 密鑰
APAJFZPFBHMFQR-UHFFFAOYSA-N
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應用
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。
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
其他客户在看
Regioselective synthesis of novel functionalized phosphanylidene anthra [2, 1-b] furan derivatives under solvent-free conditions
Nourmohammadian F and Gholami MD
Phosphorus, Sulfur, and Silicon and the Related Elements, 185(2), 340-346 (2010)
A D Ayrton et al.
Biochimica et biophysica acta, 916(3), 328-331 (1987-12-18)
Consideration of the computer-optimised dimensions of anthraflavic acid indicates that it is essentially a planar molecule with a large area/depth ratio, that would preferentially interact with the polycyclic aromatic hydrocarbon-induced family of cytochrome P-450 proteins (cytochromes P-448). Anthraflavic acid was
A D Ayrton et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 26(11-12), 909-915 (1988-11-01)
Administration of the antimutagen anthraflavic acid to rats gave rise to significant increases in the hepatic microsomal O-deethylations of ethoxyresorufin and ethoxycoumarin, but not in the O-dealkylation of pentoxyresorufin nor in cytosolic glutathione S-transferase activity. Immunoblot studies of solubilized microsomes
M Das et al.
Cancer research, 47(3), 767-773 (1987-02-01)
Naturally occurring plant phenols such as tannic acid, quercetin, myricetin, and anthraflavic acid are known to inhibit the mutagenicity of several bay-region diol-epoxides of polycyclic aromatic hydrocarbons (PAHs). The binding of bay-region diol-epoxides of PAHs to target tissue DNA is
Synthesis of tetrahydroxy-?-extended tetrathiafulvalenes as new supramolecular redox building blocks
Diaz Marta C, et al.
Tetrahedron Letters, 44(5), 945-948 (2003)
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