C99000
环庚酮
99%
别名:
琥珀酮, 酮七亚甲基, 酮环庚烷
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关于此项目
线性分子式:
C7H12(=O)
化学文摘社编号:
分子量:
112.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-937-6
Beilstein/REAXYS Number:
969823
MDL number:
Assay:
99%
Form:
liquid
form
liquid
InChI
1S/C7H12O/c8-7-5-3-1-2-4-6-7/h1-6H2
InChI key
CGZZMOTZOONQIA-UHFFFAOYSA-N
SMILES string
O=C1CCCCCC1
assay
99%
Quality Level
bp
179 °C (lit.)
density
0.951 g/mL at 25 °C (lit.)
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 3
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
131.0 °F
flash_point_c
55 °C
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
法规信息
危险化学品
此项目有
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
Takuya Hashimoto et al.
Journal of the American Chemical Society, 131(18), 6614-6617 (2009-04-22)
Insertion of one methylene unit into the C-C bond of cyclohexanones is a potentially useful, straightforward method for the construction of seven-membered carbocycles. An especially appealing but largely unexplored method in this arena is the nucleophilic addition of diazoalkanes to
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)
M Juza
Journal of chromatography. A, 865(1-2), 35-49 (2000-02-16)
A binary test mixture consisting of cyclopentanone and cycloheptanone is used for the performance evaluation of a pilot-scale simulated moving bed unit. The involved adsorption equilibria and the kinetic behavior are discussed in detail. The results of the test runs
Avidor Shulman et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 8(1), 229-239 (2002-02-02)
Antibody 38C2 efficiently catalyzes deuterium-exchange reactions at the alpha position of a variety of ketones and aldehydes, including substrates that have a variety of sensitive functional groups. In addition to the regio- and chemoselectivity of these reactions, the catalytic rates
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