544639
Methanesulfonylacetone
97%
Synonym(s):
1-(Methylsulfonyl)-2-propanone, NSC 35395
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10 G
$90.80
About This Item
Linear Formula:
CH3C(O)CH2SO2CH3
CAS Number:
Molecular Weight:
136.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
97%
form
powder or crystals
mp
48-52 °C (lit.)
functional group
ketone
sulfone
SMILES string
CC(=O)CS(C)(=O)=O
InChI
1S/C4H8O3S/c1-4(5)3-8(2,6)7/h3H2,1-2H3
InChI key
NWEYGXQKFVGUFR-UHFFFAOYSA-N
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General description
Methanesulfonylacetone is a sulfonyl group-containing active methylene compound. It can react with Baylis–Hillman acetates in dimethylformamide/potassium carbonate system to form ortho-hydroxyacetophenone derivatives.[1]
Application
Methanesulfonylacetone may be used in the preparation of 6-bromo-3-methanesulfonyl-2-methyl-quinolin-4-ol.[2]
Reactant for:
- Stereoselective preparation of chiral cyclic ketones
- Preparation of poly-substituted pyridines
- Multicomponent cyclocondensation with aldehydes and aminoazoles
- Gold-catalyzed Friedlander cyclocondensation reaction
- Radical homoallylation reactions
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Find documentation for the products that you have recently purchased in the Document Library.
New vistas in quinoline synthesis.
Atechian S, et al.
Tetrahedron, 63(13), 2811-2823 (2007)
Synthesis of ortho-hydroxyacetophenone derivatives from Baylis?Hillman acetates.
Kim JN, et al.
Tetrahedron Letters, 43(37), 6597-6600 (2007)
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