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C99000

Sigma-Aldrich

Cycloheptanone

99%

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Linear Formula:
C7H12(=O)
CAS Number:
Molecular Weight:
112.17
Beilstein:
969823
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

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

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1 of 4

This Item
CX2335475378176613
Cycloheptanone 99%

Sigma-Aldrich

C99000

Cycloheptanone

Cyclohexanone Meets ACS Specifications GR ACS

Supelco

CX2335

Cyclohexanone

Cyclohexanone-d10 98 atom % D

Sigma-Aldrich

475378

Cyclohexanone-d10

form

liquid

form

liquid

form

-

form

-

refractive index

n20/D 1.461 (lit.)

refractive index

-

refractive index

n20/D 1.45 (lit.)

refractive index

n20/D 1.449 (lit.)

bp

179 °C (lit.)

bp

155 °C/1013 hPa

bp

155 °C (lit.)

bp

153 °C (lit.)

density

0.951 g/mL at 25 °C (lit.)

density

0.95 g/cm3 at 20 °C

density

1.044 g/mL at 25 °C

density

0.986 g/mL at 25 °C

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

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
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)
K D Holland et al.
Molecular pharmacology, 37(1), 98-103 (1990-01-01)
The convulsant and/or anticonvulsant activity of unsubstituted and mono-alkyl-substituted cyclopentanones and cyclohexanones were examined by testing the ability of these compounds to produce seizures or to inhibit seizures induced by pentylenetetrazol and maximal electroshock in CF-1 mice. In addition, these
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

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