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517925

4′-Methylpropiophenone

90%, technical grade

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About This Item

Linear Formula:
CH3C6H4COC2H5
CAS Number:
5337-93-9
Molecular Weight:
148.20
NACRES:
NA.22
PubChem Substance ID:
24873986
UNSPSC Code:
12352100
EC Number:
226-267-5
MDL number:
MFCD00009312
Assay:
90%
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grade

technical grade

Quality Level

100

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

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.
  • Mono and trinuclear cobaloxime/organocobaloxime complexes, which are used as efficient catalysts for the synthesis of cyclic carbonates.
  • Tolperisone (TOL) via acid-catalyzed reaction with piperidine hydrochloride and 1,2-dioxolane.

Other Notes

Remainder 3′-methylpropiophenone

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

228.2 °F - closed cup

flash_point_c

109.00 °C - closed cup

ppe

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Certificates of Analysis (COA)

Lot/Batch Number
MKBS5733V
MKBS5734V
MKBS0722V
MKBQ2645V
MKBP0477V

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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)
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)
Discovery and structural optimization of 1-phenyl-3-(1-phenylethyl) urea derivatives as novel inhibitors of CRAC channel
Zhang Hai-zhen, et al.
Acta Pharmacologica Sinica, 36(9), 1137-1144 (2015)
View All Related Papers

Global Trade Item Number

SKUGTIN
517925-100ML04061832541754