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Key Documents

245542

Sigma-Aldrich

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

97%

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About This Item

Linear Formula:
(CH3)2C6H6(=O)
CAS Number:
Molecular Weight:
124.18
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

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.)

functional group

ketone

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

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

147.2 °F - closed cup

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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