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Merck
CN

141062

蒽

ReagentPlus®, 99%

别名:

蒽, 蒽醌

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关于此项目

经验公式（希尔记法）:
C14H10
化学文摘社编号:
120-12-7
分子量:
178.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57647135
eCl@ss:
39011608
EC Number:
204-371-1
MDL number:
MFCD00001240
Colour Index Number:
10790
Beilstein/REAXYS Number:
1905429
Assay:
99%
Form:
powder or flakes

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Quality Level

200

InChI key

MWPLVEDNUUSJAV-UHFFFAOYSA-N

InChI

1S/C14H10/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-10H

SMILES string

c1ccc2cc3ccccc3cc2c1

vapor density

6.15 (vs air)

vapor pressure

1 mmHg ( 145 °C)

product line

ReagentPlus®

assay

99%

form

powder or flakes

autoignition temp.

1004 °F

color

blue-violet fluorescence

bp

340 °C (lit.)

Gene Information

human ... CYP1A2(1544)

solubility

toluene: soluble 20 mg/mL, clear, colorless to faintly yellow, alcohols: soluble, benzene: soluble, chloroform: soluble, hydronaphthalenes: soluble, supercritical carbon dioxide: soluble

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General description

蒽衍生物可用于制备稳定的蓝光发射有机电致发光器件 。 分枝杆菌 sp 将其氧化为蒽 顺式 -1,2-二氢二醇。菌株 PYR-12 。它通过与[5,6]-富勒烯C60的[4 + 2]-环加成反应形成双加合物。

Application

蒽已被证明可溶于各种环己酮、乙酸乙酯和甲醇的二元和三元混合物中。
蒽用于研究蒽在超临界CO2中的光二聚反应。

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

249.8 °F - closed cup

flash_point_c

121.0 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

pictograms

Environment
GHS09

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - PBT

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000520882
0000520882
0000515645
0000515645
0000496449

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Anthracene derivatives for stable blue-emitting organic electroluminescence devices.
Jianmin S and Tang CW.
Applied Physics Letters, 80(17), 3201-3203 (2002)
Christopher E. Bunker et al.
The Journal of organic chemistry, 62(21), 7324-7329 (2001-10-24)
The photodimerization reaction of anthracene in supercritical CO(2) was studied systematically at different CO(2) densities. Unlike in normal liquid solvents, the reaction in supercritical CO(2) is significant even at anthracene concentrations as low as a few micromolar. At comparable anthracene
J D Moody et al.
Applied and environmental microbiology, 67(4), 1476-1483 (2001-04-03)
Cultures of Mycobacterium sp. strain PYR-1 were dosed with anthracene or phenanthrene and after 14 days of incubation had degraded 92 and 90% of the added anthracene and phenanthrene, respectively. The metabolites were extracted and identified by UV-visible light absorption
The bis-adducts of the [5, 6]-fullerene C60 and anthracene.
Duarte-Ruiz A, et al.
Tetrahedron, 57(17), 3709-3714 (2001)
Jiang-Fei Xu et al.
Organic letters, 15(24), 6148-6151 (2013-11-19)
Dynamic covalent bonds supplied by reversible anthracene dimerization were combined with pillar[5]arene/imidazole host-guest interactions to construct double-dynamic polymers. Heating such polymers (in solution or as a gel) led to depolymerization by dissociation of either the host-guest complexes alone or the
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Dihydropinene Pinane Greener Solvent for Organic Synthesis

Effective in key synthesis reactions like Knoevenagel condensation, thalidomide synthesis, and Suzuki coupling for sustainable chemical transformations.

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