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245542

Sigma-Aldrich

4,4-Dimethyl-2-cyclohexen-1-one

97%

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Linear Formula:
(CH3)2C6H6(=O)
CAS Number:
1073-13-8
Molecular Weight:
124.18
MDL number:
MFCD00009695
PubChem Substance ID:
24854739

Assay

97%

refractive index

n20/D 1.473 (lit.)

bp

72-73.5 °C/20 mmHg (lit.)

density

0.944 g/mL at 25 °C (lit.)

SMILES string

CC1(C)CCC(=O)C=C1

InChI

1S/C8H12O/c1-8(2)5-3-7(9)4-6-8/h3,5H,4,6H2,1-2H3

InChI key

HAUNPYVLVAIUOO-UHFFFAOYSA-N

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1 of 4

This Item
D154008771368336521
4,4-Dimethyl-2-cyclohexen-1-one 97%

Sigma-Aldrich

245542

4,4-Dimethyl-2-cyclohexen-1-one

3,5-Dimethyl-2-cyclohexen-1-one 98%

Sigma-Aldrich

D154008

3,5-Dimethyl-2-cyclohexen-1-one

2-Methyl-2-cyclohexen-1-one ≥90%

Sigma-Aldrich

771368

2-Methyl-2-cyclohexen-1-one

4,4-Dimethyl-2-cyclopenten-1-one 99%

Sigma-Aldrich

336521

4,4-Dimethyl-2-cyclopenten-1-one

refractive index

n20/D 1.473 (lit.)

refractive index

n20/D 1.483 (lit.)

refractive index

n20/D 1.487

refractive index

n20/D 1.457 (lit.)

bp

72-73.5 °C/20 mmHg (lit.)

bp

211-212 °C (lit.)

bp

176-179 °C/760 mmHg

bp

158 °C (lit.)

density

0.944 g/mL at 25 °C (lit.)

density

0.881 g/mL at 25 °C (lit.)

density

0.972 g/mL at 25 °C

density

0.903 g/mL at 25 °C (lit.)

Quality Level

200

Quality Level

100

Quality Level

-

Quality Level

100

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(C)

64 °C - closed cup

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Guifang Zhang et al.
Investigative ophthalmology & visual science, 48(11), 5243-5249 (2007-10-27)
To describe a method of drug delivery to the retina via aerosolized nanoparticles in the gas phase during the gas-exchange stage of vitrectomy in a porcine model. An ultrasonically atomized and dried sodium fluorescein aerosol was produced with a concentration
Studies on the reactions of α, β-enones with allyl indium reagent; effects of TMSCl as promoter on regioselectivity.
Lee PH, et al.
Tetrahedron Letters, 42(1), 37-39 (2001)
Borja Oliver-Tomas et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(52), 12900-12908 (2017-07-06)
For the reaction mechanism of the ketonic decarboxylation of two carboxylic acids, a β-keto acid is favored as key intermediate in many experimental and theoretical studies. Hydrogen atoms in the α-position are an indispensable requirement for the substrates to react

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