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1-Acetylpyren

97%

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About This Item

Empirische Formel (Hill-System):
C18H12O
CAS-Nummer:
3264-21-9
Molekulargewicht:
244.29
MDL-Nummer:
MFCD00021663
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24864377
NACRES:
NA.22

Assay

97%

Form

solid

mp (Schmelzpunkt)

86-89 °C (lit.)

SMILES String

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

InChIKey

KCIJNJVCFPSUBQ-UHFFFAOYSA-N

Verwandte Kategorien

Allgemeine Beschreibung

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.

Anwendung

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.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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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)
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)
Fundamental photoluminescence properties of pyrene carbonyl compounds through absolute fluorescence quantum yield measurement and density functional theory.
Niko Y, et al.
Tetrahedron, 68(31), 6177-6185 (2012)
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
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