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D146706

Sigma-Aldrich

9,10-Dimethylanthracene

99%

Sinónimos:

9,10-Dimethylanthracene

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About This Item

Fórmula empírica (notación de Hill):
C16H14
Número de CAS:
781-43-1
Peso molecular:
206.28
Beilstein/REAXYS Number:
1909028
EC Number:
212-308-4
MDL number:
MFCD00001262
UNSPSC Code:
12352100
PubChem Substance ID:
24893449
NACRES:
NA.22

assay

99%

form

crystals

mp

182-184 °C (lit.)

SMILES string

Cc1c2ccccc2c(C)c3ccccc13

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

InChI key

JTGMTYWYUZDRBK-UHFFFAOYSA-N

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pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Resp. Sens. 1 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Certificados de análisis (COA)

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Alan Sholto et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 7(3), 344-351 (2008-04-05)
Six amphiphilic silicon phthalocyanines (SiPc's) axially linked to a dimethylated amino alkyl group of varying length have been examined for their potential suitability as photosensitizers for photodynamic therapy (PDT). This group of molecules was chosen because the length of the
David Bailey et al.
Chemical communications (Cambridge, England), (20)(20), 2569-2571 (2005-05-19)
Irradiating 2,3,6,7-tetraphenylanthracene in the presence of 9,10-dimethylanthracene leads to exclusive formation of the cross-dimer. No photochemical reaction is observed when either of these chromophores is irradiated in the absence of the other.
E Gross et al.
Photochemistry and photobiology, 57(5), 808-813 (1993-05-01)
Two new sensitizers are introduced for a potential use in photodynamic therapy: Zn(2+)- and MG(2+)-tetrabenzoporphyrin (ZnTBP and MgTBP). A comparative study of the quantum yields of singlet oxygen generation (phi delta) of hematoporphyrin derivative (HpD), Photofrin II (PF-II), Zn(2+)-phthalocyanine tetrahydroxyl
E W Vogel et al.
Mutation research, 250(1-2), 291-298 (1991-09-01)
A set of six Drosophila strains was developed, by inducing by chemical treatment with N-ethyl-N-nitrosourea (ENU) new white and, in some strains, yellow mutations in 3 wild-type (WT) and 3 insecticide-resistant (IR) populations. These strains were previously shown to vary
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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