180610
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:
Molecular Weight:
270.32
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
222-055-1
Beilstein/REAXYS Number:
1985273
MDL number:
InChI key
AIGDHFJPKNZUOR-UHFFFAOYSA-N
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
SMILES string
O=C1CCCc2c1cc3ccc4cccc5ccc2c3c45
assay
97%
Application
Precursor to benzo[a]pyrene derivatives.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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The Journal of Organic Chemistry, 58, 7283-7283 (1993)
Large polycyclic aromatic hydrocarbons: synthesis and discotic organization
Feng, X., Pisula, W., & Mullen, K.
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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
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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
Xue Zhao et al.
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