245542
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
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Product Name
4,4-Dimethyl-2-cyclohexen-1-one, 97%
InChI
1S/C8H12O/c1-8(2)5-3-7(9)4-6-8/h3,5H,4,6H2,1-2H3
SMILES string
CC1(C)CCC(=O)C=C1
InChI key
HAUNPYVLVAIUOO-UHFFFAOYSA-N
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
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
147.2 °F - closed cup
flash_point_c
64 °C - closed cup
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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.
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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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