China supplier 4-Methylpropiophenone 5337-93-9 (1-(p-Tolyl)propan-1-one 1-(4-methylphenyl)propan-1
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4-Methylpropiophenone
1-(p-Tolyl)propan-1-one
1-(4-methylphenyl)propan-1-one
4'-Methylpropiophenone
EINECS 226-267-5
MFCD00009312
1-(4-Methylphenyl)-1-propanone
1-Propanone, 1-(4-methylphenyl)-
p-Tolyl ethyl ketone
1-(p-tolyl)propan-1-on
p-methylpropiophenone
what is 4-methylpropiophenone ?
4-methylpropiophenone is an aromatic ketone that is propiophenone bearing a methyl group at C-4. It derives from a propiophenone
4-methylpropiophenone uses
4-Methylpropiophenone is a chemical reagent used in electrocarboxylation reactions. It is as a raw material for organic synthesis of agrochemicals, pharmaceuticals and dyestuff.
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What is 4-Methylpropiophenone CAS 5337-93-9?
4-Methylpropiophenone, also known as 4'-Methylpropiophenone Cas 5337-93-9, 4-Methylpropiophenone Cas 5337-93-9, p-Methylpropiophenone Cas 5337-93-9. It is It is an organic intermediate, which can be obtained from pentanone as raw material and p-methyl. It is reported to be used in the preparation of histone demethylase inhibitors. Its CAS number is 5337-93-9, molecular weight is 148.2 g/mol, and molecular formula is C10H12O. 4'-Methylpropiophenone Cas 5337-93-9 is used as organic reagent for qualitative or quantitative determination of chemical elements and for separation, enrichment and concealment of organic compounds. This product is widely used in various fields, as well as fragrances, and organic reagents. In terms of usage, organic reagents can be used as indicator, precipitant, titrant, colorant, extractant, adsorbent and concealer. In terms of reaction mechanism, organic reagents are mainly complexation reactions, from monotypic binary di-chelates to multi-chelates (see chelation) and multi-complexes, with an increasingly wide range of applications . The following is a brief description of 4'-methylpropiophenone Cas 5337-93-9.
How to Make 4 Methylpropiophenone?
Production of 4-Methylpropiophenone
4-Methylpropiophenone is prepared via Friedel Craft reaction for Toluene and propionyl chloride, in the presence of Aluminium Chloride as a catalyst.
