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Merck
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주요 문서

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P10801

Sigma-Aldrich

Perinaphthenone

97%

동의어(들):

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

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모든 사진(1)

About This Item

실험식(Hill 표기법):
C13H8O
CAS Number:
548-39-0
Molecular Weight:
180.20
EC Number:
208-945-2
MDL number:
MFCD00004143
UNSPSC 코드:
12352100
PubChem Substance ID:
24898151
NACRES:
NA.22

Quality Level

100

분석

97%

양식

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

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
STBH9725
STBD2936V
STBC1138V
STBB9087V
STBB9087

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9-Fluorenone 98%

Sigma-Aldrich

F1506

9-Fluorenone

Mahmoud Fahmi Elsebai et al.
Organic & biomolecular chemistry, 9(3), 802-808 (2010-11-26)
The marine-derived fungus Coniothyrium cereale was isolated from the green alga Enteromorpha sp. and found to produce the new phenalenone derivatives 1-7 as well as the known compounds lactone 8, (-) sclerodin (9), lamellicolic anhydride (10), (-) scleroderolide (11), and
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
Zhiyong Guo et al.
Magnetic resonance in chemistry : MRC, 45(5), 439-441 (2007-03-21)
The complete (1)H and (13)C NMR assignments are reported for the novel natural product Bacillosporin D together with the known compound Bacillosporin C. These compounds containing seven rings were isolated from the mangrove endophytic fungus SBE-14 from the South China
Cristina Flors et al.
Accounts of chemical research, 39(5), 293-300 (2006-05-17)
Plants defend themselves from pathogen infections or mechanical injury by a number of mechanisms, including the induced biosynthesis of antimicrobial secondary metabolites. These compounds, termed phytoalexins, represent a very economical way to counteract hazard, because the carbon and energy resources
William Hidalgo et al.
Journal of agricultural and food chemistry, 57(16), 7417-7421 (2009-07-28)
The levels of native fungitoxic perinaphthenone phytoalexins in susceptible Musa varieties (banana), which are commercially grown in large plantations, are too low to provide plants with long-lasting protection against highly pathogenic fungi. Novel strategies for plant protection are necessary to
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