所有图片(1)
About This Item
经验公式（希尔记法）:
C18H12O
CAS号:
分子量:
244.29
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
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)
Synthesis and study of film-forming properties and light sensitivity of 4-acyloxy-3-methoxy (ethoxy) phenylmethylidene-(chrysen-2-yl) amines.
Dikusar EA, et al.
Russ. J. Gen. Chem., 77(2), 278-281 (2007)
H Surya Prakash Rao et al.
Beilstein journal of organic chemistry, 3, 31-31 (2007-10-02)
The cycloaddition of the von Leusen's reagent (p-tolylsulfonyl)methyl isocyanide (TosMIC) to alpha-aroylketene dithioacetals (AKDTAs) in the presence of sodium hydride in THF at rt resulted in a facile synthesis of the 4-aroyl-3-methylsulfanyl-2-tosylpyrroles 3 in good yield along with a minor
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)
Synthesis, characterization and pharmacological investigations of some novel heterocyclic derivatives incorporating pyrene and sugar moieties.
Khalifa NM, et al.
Research on Chemical Intermediates, 40(4), 1565-1574 (2014)
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