C99000
Cycloheptanone
99%
Synonym(s):
Ketocycloheptane, Ketoheptamethylene, Suberone
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About This Item
Linear Formula:
C7H12(=O)
CAS Number:
Molecular Weight:
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
Quality Level
assay
99%
form
liquid
refractive index
n20/D 1.461 (lit.)
bp
179 °C (lit.)
density
0.951 g/mL at 25 °C (lit.)
SMILES string
O=C1CCCCCC1
InChI
1S/C7H12O/c8-7-5-3-1-2-4-6-7/h1-6H2
InChI key
CGZZMOTZOONQIA-UHFFFAOYSA-N
Related Categories
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 3
Storage Class
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)
Regulatory Information
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
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
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| C99000-100G | 04061833531334 |
| C99000-250G | 04061836696160 |
| C99000-25G | 04061833531341 |
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