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P10801

Sigma-Aldrich

Perinaphthenone

97%

Synonym(s):

1H-Benzonaphthen-1-one, 7-Perinaphthenone, Phenalenone, Phenalone

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About This Item

Empirical Formula (Hill Notation):
C13H8O
CAS Number:
Molecular Weight:
180.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

powder

mp

153-156 °C (lit.)

SMILES string

O=C1C=Cc2cccc3cccc1c23

InChI

1S/C13H8O/c14-12-8-7-10-4-1-3-9-5-2-6-11(12)13(9)10/h1-8H

InChI key

WWBGWPHHLRSTFI-UHFFFAOYSA-N

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Stefan Opitz et al.
Journal of natural products, 65(8), 1122-1130 (2002-08-24)
Phytochemical analysis of Xiphidium caeruleum, a neotropical member of the family Haemodoraceae, resulted in the isolation and identification of a variety of phenylphenalenone-related compounds. The structures of four new phenylbenzoisochromenones (3, 6, 7, 10), a new phenylbenzoisoquinolinone (4), and two
Kentaro Misaki et al.
Mutagenesis, 23(5), 359-366 (2008-05-16)
1H-Phenalen-1-one (phenalenone) is one of the major oxygenated polyaromatic compounds present in the atmospheric environment. In order to gain detailed information regarding the mutagenicity and physicochemical properties of the nitration products of phenalenone, we measured Ames Salmonella mutagenicity, lower LUMO
Felipe Otálvaro et al.
Journal of natural products, 70(5), 887-890 (2007-04-13)
Two perinaphthenone-type compounds (1 and 2) were isolated together with four known phenylphenalenones (3-6) from the rhizomes of Musa acuminata var. "Yangambi km 5". The structures of the new phenalenones were assigned as 2-hydroxy-1H-phenalen-1-one (1) and 2-methoxy-1H-phenalen-1-one (2) on the
Deski Beri et al.
Frontiers in chemistry, 8, 567-567 (2020-08-09)
Silicon nanocrystals (SiNCs) are regarded as a green and environmentally friendly material when compared with other semiconductor nanocrystals. Ultra-small SiNCs (with the size 4.6-5.2 nm) demonstrate strong UV absorption and photoluminescence in the near infrared (NIR) range with the high
Christopher M Whidbey et al.
Water research, 46(16), 5287-5296 (2012-08-11)
Steroid estrogens are endocrine disrupting contaminants frequently detected in natural waters. Because these estrogens can elicit significant biological responses in aquatic organisms, it is important to study their rates and pathways of degradation in natural waters and to identify whether

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