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Merck
CN

P10801

Sigma-Aldrich

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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About This Item

经验公式(希尔记法):
C13H8O
CAS号:
分子量:
180.20
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

表单

powder

mp

153-156 °C (lit.)

SMILES字符串

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

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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
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
Xiaopeng Chen et al.
Chemical communications (Cambridge, England), 47(9), 2628-2630 (2011-01-15)
Phenalenone derivatives were efficiently constructed from 1,8-diiodonaphthalene and tertiary propynols via a one-pot domino reaction which eventually included Pd-catalyzed Sonogoshira coupling, Pd-catalyzed allylic oxidation and Pd-catalyzed C(sp(2))-H activation. Moreover, the synthesized phenalenone derivative presented a practical application as a fluorescent

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