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C99000

Sigma-Aldrich

Cycloheptanone

99%

Sinónimos:

Ketocycloheptane, Ketoheptamethylene, Suberone

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About This Item

Fórmula lineal:
C7H12(=O)
Número de CAS:
502-42-1
Peso molecular:
112.17
Beilstein/REAXYS Number:
969823
EC Number:
207-937-6
MDL number:
MFCD00004159
UNSPSC Code:
12352100
PubChem Substance ID:
24893205
NACRES:
NA.22

Quality Level

100

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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pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

hcodes

H226,H302

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

131.0 °F

flash_point_c

55 °C

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
STBK6043
STBK5768
S45944
11527TD
07715JD

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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
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
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
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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