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180610

Sigma-Aldrich

9,10-Dihydrobenzo[a]pyrene-7(8H)-one

97%

Synonym(s):

7-Oxo-7,8,9,10-tetrahydrobenzo[a ]pyrene

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About This Item

Empirical Formula (Hill Notation):
C20H14O
CAS Number:
3331-46-2
Molecular Weight:
270.32
Beilstein/REAXYS Number:
1985273
EC Number:
222-055-1
MDL number:
MFCD00003601
UNSPSC Code:
12352103
PubChem Substance ID:
24850880
NACRES:
NA.23

assay

97%

mp

172-175 °C (lit.)

SMILES string

O=C1CCCc2c1cc3ccc4cccc5ccc2c3c45

InChI

1S/C20H14O/c21-18-6-2-5-15-16-10-9-13-4-1-3-12-7-8-14(11-17(15)18)20(16)19(12)13/h1,3-4,7-11H,2,5-6H2

Inchi Key

AIGDHFJPKNZUOR-UHFFFAOYSA-N

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Application

Precursor to benzo[a]pyrene derivatives.[1]

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
03802JZ
11211CZ
00316MY
07610BL
07011KF

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The Journal of Organic Chemistry, 58, 7283-7283 (1993)
Khin K Chin et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 7(1), 49-55 (2008-01-03)
The photophysical properties of a novel series of non-homoconjugated 1,2-di-, 1,2,3,4-tetra-, and 1,2,3,4,5,6-hexasubstituted fullerenes (compounds 1, 2, and 3, respectively) have been systematically investigated. In this report, we examine the effect of substitution pattern of non-homoconjugated derivatized fullerenes on the
Y L Ha et al.
Cancer research, 50(4), 1097-1101 (1990-02-15)
Grilled ground beef contains factors that inhibit the initiation of mouse epidermal carcinogenesis by 7,12-dimethylbenz(a)anthracene. Previously we isolated an active principal and characterized it as an isomeric mixture of conjugated dienoic derivatives of linoleic acid (CLA). We now show that
Xue Zhao et al.
Food chemistry, 239, 781-788 (2017-09-07)
Changes in polycyclic (PAH) and oxygenated (OPAH) aromatic hydrocarbon concentrations in vegetable oils during storage for 270days at 25°C or 4°C were investigated. The concentrations of OPAHs and PAHs increased with storage time. The increase in PAH concentration was mainly
Large polycyclic aromatic hydrocarbons: synthesis and discotic organization
Feng, X., Pisula, W., & Mullen, K.
Pure and Applied Chemistry. Chimie Pure Et Appliquee, 81(12), 2203-2224 (2009)
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