P10801
萘嵌苯酮
97%
别名:
1H-苯并萘-1-酮, 7-萘酚酮, 苯丙烯酮, 苯丙酮
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关于此项目
经验公式（希尔记法）:
C13H8O
化学文摘社编号:
分子量:
180.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
208-945-2
MDL number:
Assay:
97%
Form:
powder
InChI key
WWBGWPHHLRSTFI-UHFFFAOYSA-N
InChI
1S/C13H8O/c14-12-8-7-10-4-1-3-9-5-2-6-11(12)13(9)10/h1-8H
SMILES string
O=C1C=Cc2cccc3cccc1c23
assay
97%
form
powder
mp
153-156 °C (lit.)
Quality Level
Application
萘嵌苯酮可用于：
- 以gem-二氢过氧化物为化学计量氧化剂，通过Weitz-Scheffer环氧化作用合成相应的环氧化物。
- 作为戊唑醇光降解中的光敏剂。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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
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
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
Mahmoud F Elsebai et al.
Natural product reports, 31(5), 628-645 (2014-04-02)
Covering up to the end of August 2013. Phenalenones are members of a unique class of natural polyketides exhibiting diverse biological potential. This is a comprehensive review of 72 phenalenones with diverse structural features originating from fungal sources. Their bioactive
S Opitz et al.
Planta, 216(5), 881-889 (2003-03-08)
Phenylphenalenones represent a typical group of secondary metabolites of the Haemodoraceae. Some of these phenolic compounds show organ-specific distribution within the plant. However, detailed information on cellular localisation is still lacking. To this end, confocal laser-scanning microscopy, microspectral photometry and
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