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C99000

Sigma-Aldrich

Cycloheptanone

99%

Synonym(s):

Ketocycloheptane, Ketoheptamethylene, Suberone

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About This Item

Linear Formula:
C7H12(=O)
CAS Number:
502-42-1
Molecular Weight:
112.17
Beilstein:
969823
EC Number:
207-937-6
MDL number:
MFCD00004159
UNSPSC Code:
12352100
PubChem Substance ID:
24893205
NACRES:
NA.22

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

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Related Categories

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H302

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

131.0 °F

Flash Point(C)

55 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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
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
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
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
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