D146706
9,10-二甲基蒽
99%
别名:
9,10-二甲基蒽
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关于此项目
经验公式（希尔记法）:
C16H14
化学文摘社编号:
分子量:
206.28
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-308-4
Beilstein/REAXYS Number:
1909028
MDL number:
产品名称
9,10-二甲基蒽, 99%
assay
99%
InChI key
JTGMTYWYUZDRBK-UHFFFAOYSA-N
InChI
1S/C16H14/c1-11-13-7-3-5-9-15(13)12(2)16-10-6-4-8-14(11)16/h3-10H,1-2H3
SMILES string
Cc1c2ccccc2c(C)c3ccccc13
form
crystals
mp
182-184 °C (lit.)
Quality Level
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flash_point_c
Not applicable
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Resp. Sens. 1 - Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
A smart polysaccharide/drug conjugate for photodynamic therapy.
So Young Park et al.
Angewandte Chemie (International ed. in English), 50(7), 1644-1647 (2011-02-11)
Sankarasharma Devipriya et al.
Chemico-biological interactions, 162(2), 106-113 (2006-07-19)
Administration of quercetin, a common polyphenolic component of many vascular and edible plants including vegetables, fruits and tea significantly reduced the tumor volume in rats induced for mammary carcinoma using dimethyl benz (a) anthracene (DMBA). Dose response was assessed, by
R K Saini et al.
Drug and chemical toxicology, 31(4), 459-471 (2008-10-14)
A single intratracheal instillation of 9,10-dimethyl benz(a)anthracene (DMBA) at 3 different doses of 5, 10, and 20 mg/kg body weight to Balb/c mice for 12 weeks had caused a significant incidence of pulmonary tumors along with inflammatory changes. The number
Shimshon Ben Dror et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 8(3), 354-361 (2009-03-04)
In this work we investigate the localization and photophysical properties of twelve synthetically derived chlorins in artificial membranes, with the goal of designing more effective photosensitizers for photodynamic therapy (PDT). The studied chlorins incorporate substituents of varying lipophilicity at the
M Elisa Milanesio et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2(9), 926-933 (2003-10-17)
A novel 5-[4-(trimethylammonium)phenyl]-10,15,20-tris(2,4,6-trimethoxyphenyl)porphyrin iodide (2) has been synthesized. A positive charge was incorporated at a peripheral position to increase the amphiphilic character of the structure. The photodynamic effect of the cationic porphyrin 2 was compared with that of non-charged 5-(4-aminophenyl)-10,15,20-tris(2,4,6-trimethoxyphenyl)porphyrin
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