Merck
CN

C99000

Sigma-Aldrich

环庚酮

99%

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别名:
Ketocycloheptane, Ketoheptamethylene, Suberone
线性分子式:
C7H12(=O)
CAS号:
分子量:
112.17
Beilstein:
969823
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99%

形式

liquid

折射率

n20/D 1.461 (lit.)

bp

179 °C (lit.)

密度

0.951 g/mL at 25 °C (lit.)

SMILES字符串

O=C1CCCCCC1

InChI

1S/C7H12O/c8-7-5-3-1-2-4-6-7/h1-6H2

InChI key

CGZZMOTZOONQIA-UHFFFAOYSA-N

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象形图

FlameExclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral - Flam. Liq. 3

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

131.0 °F

闪点(°C)

55 °C

个人防护装备

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

法规信息

危险化学品

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Brian T Sullivan et al.
Journal of chemical ecology, 47(1), 10-27 (2021-01-07)
We investigated geographic variation in the semiochemistry of major disturbance agents of western North American pine forests, Dendroctonus brevicomis Le Conte and Dendroctonus barberi Hopkins (Coleoptera: Curculionidae: Scolytinae), species separated by the Great Basin in the USA that until recently
R Singh et al.
Current medicinal chemistry. Anti-cancer agents, 3(6), 431-438 (2003-10-08)
A series of naturally occurring and synthetic novel oxapenam (4-oxa-1-azabicyclo[3.2.0] heptan-7-one) derivatives with their antitumor activity and the structure-activity relationship among this class of compounds is reported. Among the synthetic 4-oxa-1-azabicyclo[3.2.0]heptan-7-one having an ester, amide, ether derivatives of hydroxy group
Richmond Sarpong et al.
Journal of the American Chemical Society, 125(45), 13624-13625 (2003-11-06)
A set of mild processes for the conversion of vinyl cyclopropyl diazo ketones to highly functionalized cycloheptadienones and vinyl cyclopentenones by use of a target-inspired tandem Wolff/Cope rearrangement sequence is described. A divergent reaction course of the vinyl cyclopropyl diazo
Redouane Beniazza et al.
The Journal of organic chemistry, 76(3), 791-799 (2011-01-13)
A short access to homocalystegine analogues silylated at C7 is described. The synthesis involves the desymmetrization of a (phenyldimethylsilyl)methylcycloheptatriene using osmium-mediated dihydroxylation, followed by the diol protection and a cycloaddition involving the remaining diene moiety and an acylnitroso reagent. Additions
Khairia M Youssef et al.
Archiv der Pharmazie, 337(1), 42-54 (2004-02-05)
New series of 3, 5-bis(substituted benzylidene)-4-piperidones, 2, 7-bis(substituted benzylidene)cycloheptanones, 1, 5-bis(substituted phenyl)-1, 4-pentadien-3-ones, 1, 7-bis(substituted phenyl)-1, 6-heptadien-3, 5-diones, 1, 1-bis(substituted cinnamoyl)-cyclopentanes, and 1, 1-bis(substituted cinnamoyl)cyclohexanes have been synthesized and tested for their antioxidant activity. Among the tested compounds, compounds II(4)

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