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About This Item
Linear Formula:
CH3C6H4COC2H5
CAS Number:
Molecular Weight:
148.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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grade
technical grade
Quality Level
Assay
90%
refractive index
n20/D 1.528 (lit.)
bp
238-239 °C (lit.)
density
0.993 g/mL at 25 °C (lit.)
functional group
ketone
SMILES string
CCC(=O)c1ccc(C)cc1
InChI
1S/C10H12O/c1-3-10(11)9-6-4-8(2)5-7-9/h4-7H,3H2,1-2H3
InChI key
PATYHUUYADUHQS-UHFFFAOYSA-N
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Application
4′-Methylpropiophenone can be used as a building block to synthesize:
- N
- -(4-Chlorophenyl)-N′-[1-(4-methylphenyl)propyl]urea as a potential CRAC channel inhibitor.[1]
- Mono and trinuclear cobaloxime/organocobaloxime complexes, which are used as efficient catalysts for the synthesis of cyclic carbonates.[2]
- Tolperisone (TOL) via acid-catalyzed reaction with piperidine hydrochloride and 1,2-dioxolane.[3]
Other Notes
Remainder 3′-methylpropiophenone
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
228.2 °F - closed cup
Flash Point(C)
109.00 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Alkaloid induced asymmetric electrocarboxylation of 4-methylpropiophenone.
Zhao SF, et al.
Tetrahedron Letters, 52(21), 2702-2705 (2011)
TLC-densitometric determination of tolperisone and its impurities 4-methylpropiophenone and piperidine in pharmaceutical preparations
Hubicka U, et al.
Journal of Liquid Chromatography and Related Technologies, 35(10), 1325-1335 (2012)
V Karunakaran et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 128, 1-14 (2014-03-25)
Combined experimental and theoretical studies have been performed on the structure and vibrational spectra (IR and Raman spectra) of 4'-methylpropiophenone (MPP). The FT-IR and FT-Raman spectra of 4'-methylpropiophenone (MPP) have been recorded in the region 4000-400 cm(-1) and 3500-100 cm(-1)
Paul I Dargan et al.
Drug testing and analysis, 3(7-8), 454-463 (2011-07-15)
Mephedrone (4-methylmethcathinone) is a synthetic cathinone that is used as a recreational drug. It has been available since 2007 but its availability and use increased significantly during 2009 and 2010. In this review article we will summarize the available literature
Ketone synthesized cobaloxime/organocobaloxime catalysts for cyclic carbonate synthesis from CO2 and epoxides: Characterization and electrochemistry
Kilic A, et al.
Journal of Organometallic Chemistry, 767, 150-159 (2014)
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