D153303
5,5-Dimethyl-1,3-cyclohexanedione
95%
Synonym(s):
Dimedone, Methone
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All Photos(2)
About This Item
Linear Formula:
(CH3)2C6H6(=O)2
CAS Number:
Molecular Weight:
140.18
Beilstein:
471489
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
95%
form
powder
mp
146-148 °C (lit.)
SMILES string
CC1(C)CC(=O)CC(=O)C1
InChI
1S/C8H12O2/c1-8(2)4-6(9)3-7(10)5-8/h3-5H2,1-2H3
InChI key
BADXJIPKFRBFOT-UHFFFAOYSA-N
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Application
Part of furannulation strategy for the synthesis of naturally occurring fused 3-methylfurans.
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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The Journal of Organic Chemistry, 58, 3960-3960 (1993)
Kimberly J Nelson et al.
Methods in enzymology, 473, 95-115 (2010-06-02)
Reversible thiol modification is a major component of the modulation of cell-signaling pathways by reactive oxygen species. Hydrogen peroxide, peroxynitrite, or lipid hydroperoxides are all able to oxidize cysteines to form cysteine sulfenic acids; this reactive intermediate can be directly
Osama I El-Sabbagh et al.
Archiv der Pharmazie, 343(9), 519-527 (2010-09-04)
New nonclassical acridines, quinolines, and quinazolines were prepared starting from cyclic β-diketones, namely dimedone, through application of Hantzsch addition, Michael addition, and Mannich reactions, respectively. The antimicrobial activity revealed that decahydroacridin-1,8-dione 2e bearing a 3-nitrophenyl group and hexahydroquinoline 4e having
Chananat Klomsiri et al.
Methods in enzymology, 473, 77-94 (2010-06-02)
Sulfenic acids, formed as transient intermediates during the reaction of cysteine residues with peroxides, play significant roles in enzyme catalysis and regulation, and are also involved in the redox regulation of transcription factors and other signaling proteins. Therefore, interest in
Bahjat A Saeed et al.
Molecules (Basel, Switzerland), 14(6), 2278-2285 (2009-06-26)
Symmetrical and non-symmetrical diimines derived from dimedone were synthesized by the reaction of their corresponding enaminothiones with primary amines. The synthesized compounds were characterized using micro analytical data and NMR spectroscopy. Theoretical calculations by B3LYP/6-31G(d,p) level of theory show that
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