ETHYL-O-TOLYL KETONE

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ETHYL-O-TOLYL KETONE manufacturers

  • ETHYL-O-TOLYL KETONE
  • ETHYL-O-TOLYL KETONE pictures
  • $1.00
  • 2020-01-09
  • CAS:2040-14-4
  • Min. Order: 1KG
  • Purity: 98% HPLC
  • Supply Ability: 10 tons/month
ETHYL-O-TOLYL KETONE Basic information
Product Name:ETHYL-O-TOLYL KETONE
Synonyms:2'-Methylpropiophenone 98%;1-(2-Methylphenyl)propan-1-one, 2-(Ethylcarbonyl)toluene;2'-Methylpropiophenone98%;O-METHYL-PROPIOPHENONE;ETHYL-O-TOLYL KETONE;o-Methyl-propiophenone, 97 % min.;1-(2-methylphenyl)propan-1-one;Tolperisone Impurity D
CAS:2040-14-4
MF:C10H12O
MW:148.2
EINECS:
Product Categories:
Mol File:2040-14-4.mol
ETHYL-O-TOLYL KETONE Structure
ETHYL-O-TOLYL KETONE Chemical Properties
Melting point -27.6°C
Boiling point 219.5°C (estimate)
density 1.0119
refractive index 1.5413 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Sparingly), Methanol (Slightly)
form liquid
color Light Yellow
InChIInChI=1S/C10H12O/c1-3-10(11)9-7-5-4-6-8(9)2/h4-7H,3H2,1-2H3
InChIKeyVQHKICGSBBPFFJ-UHFFFAOYSA-N
SMILESC(C1=CC=CC=C1C)(=O)CC
Safety Information
HS Code 2914390090
MSDS Information
ETHYL-O-TOLYL KETONE Usage And Synthesis
Uses2'-Methylpropiophenone can be used for volatile component analysis in infant formula using SPME coupled with GCxGC-TOFMS.
Synthesis
1-(2-METHYLPHENYL)-1-PROPANOL

61017-92-3

ETHYL-O-TOLYL KETONE

2040-14-4

1-(p-formyl)ethanol (1 mmol) was used as starting material with chloramine-T (1 mmol) and In(OTf)3 (0.3 mmol) in a 100 mL round-bottomed flask fitted with a magnetic stirrer and dissolved in acetonitrile (10 mL). The reaction mixture was heated and refluxed under argon protection for 3 h. The reaction progress was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the mixture was cooled to room temperature and the solvent was removed by rotary evaporator. The residue was purified by fast column chromatography on silica gel. The final product was analyzed by spectroscopy for structural confirmation.

References[1] Journal of Organic Chemistry, 1986, vol. 51, # 9, p. 1402 - 1406
[2] Phytochemistry, 2013, vol. 96, p. 223 - 234
[3] European Journal of Medicinal Chemistry, 1995, vol. 30, # 1, p. 85 - 94
[4] Journal of Organic Chemistry, 2003, vol. 68, # 4, p. 1594 - 1596
[5] Chemical and Pharmaceutical Bulletin, 2017, vol. 65, # 8, p. 801 - 804
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