方案
97%
表单
solid
mp
86-89 °C (lit.)
官能团
ketone
SMILES字符串
CC(=O)c1ccc2ccc3cccc4ccc1c2c34
InChI
1S/C18H12O/c1-11(19)15-9-7-14-6-5-12-3-2-4-13-8-10-16(15)18(14)17(12)13/h2-10H,1H3
InChI key
KCIJNJVCFPSUBQ-UHFFFAOYSA-N
一般描述
1-Acetylpyrene is a pyrene derivative. Its synthesis has been reported. Its phytophysical properties have been studied using absolute fluorescence quantum yield measurement and time-dependent density functional theory (TD-DFT) calculations. Its ability to interact with human cytochromes P450 2A13, 2A6, and 1B1 and enzyme inhibition has been reported. Its function as an environment-sensitive fluorophore has been investigated.
应用
1-Acetylpyrene is suitable for use in a comparative study on the photoinitiating efficiency of pyrene, 1-acetylpyrene and 1-(bromoacetyl)pyrene for copolymerization of styrene with acrylonitrile. It may be used in the following studies:
- As a starting material in the synthesis of ethynlypyrene. 1-(1-chlorovinyl)pyrene was also isolated during this reaction.
- As a starting material in the synthesis of substituted pyrene derivatives incorporated heterocyclic and sugar moieties.
- Synthesis of (E)-pyrene oxime ester conjugates of carboxylic acids.
- Synthesis of tertiary alcohols based on 1-acetylpyrene.
- Synthesis of (E)-N-[1-(pyren-1-yl)ethylidene]chrysene-2-amine.
- Synthesis of 3,3-di(methylsulfanyl)-1-(1-pyrenyl)-2-propen-1-one.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
1-(Bromoacetyl) pyrene, a novel photoinitiator for the copolymerization of styrene and acrylonitrile.
Mishra A and Daswal S.
Coll. Polymer Sci., 285(4), 397-404 (2007)
Synthesis and fluorescent properties of 5-(1-pyrenylethynyl)-2'-deoxyuridine-containing oligodeoxynucleotides.
Malakhov AD, et al.
Russian J. Bioorg. Chem., 26(1), 34-44 (2000)
Tsutomu Shimada et al.
Chemical research in toxicology, 26(4), 517-528 (2013-02-26)
A total of 68 chemicals including derivatives of naphthalene, phenanthrene, fluoranthene, pyrene, biphenyl, and flavone were examined for their abilities to interact with human P450s 2A13 and 2A6. Fifty-one of these 68 chemicals induced stronger Type I binding spectra (iron
One-pot synthesis of 1-acetylpyrene over supported phosphotungstic heteropoly acid catalysts.
He MQ, et al.
Reaction Kinetics, Mechanisms and Catalysis, 108(2), 531-544 (2013)
Tertiary alcohols based on 1-acetylpyrene.
Dikusar EA.
Russ. J. Org. Chem., 43(10), 1492-1494 (2007)
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