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4-Ethylacetophenone

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4-Ethylacetophenone Basic information

Product Name:
4-Ethylacetophenone
Synonyms:
  • 1-(4-ETHYL-PHENYL)ETHANONE
  • AKOS BBS-00004394
  • 4-ETHYLACETOPHENONE
  • 4-ETHYL-1-ACETYLBENZENE
  • 1-(4-ethylphenyl)-ethanon
  • Acetophenone, 4'-ethyl-
  • p-Acetylethylbenzene
  • p-Ethylphenyl methyl ketone
CAS:
937-30-4
MF:
C10H12O
MW:
148.2
EINECS:
213-326-5
Product Categories:
  • Aromatic Acetophenones & Derivatives (substituted)
  • Adehydes, Acetals & Ketones
  • Acetophenones (Building Blocks for Liquid Crystals)
  • Building Blocks for Liquid Crystals
  • Functional Materials
  • C10
  • Carbonyl Compounds
  • Ketones
  • john's
  • K00001
Mol File:
937-30-4.mol
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4-Ethylacetophenone Chemical Properties

Melting point:
−20.6 °C(lit.)
Boiling point:
125 °C20 mm Hg(lit.)
Density 
0.993 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.5293(lit.)
Flash point:
195 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly)
form 
Oil
color 
Clear Colourless
Specific Gravity
0.993
Odor
at 1.00 % in dipropylene glycol. floral hawthorn
Odor Type
floral
Water Solubility 
Not miscible or difficult to mix in water. Soluble in alcohol.
BRN 
1906029
Cosmetics Ingredients Functions
PERFUMING
LogP
2.507 (est)
CAS DataBase Reference
937-30-4(CAS DataBase Reference)
NIST Chemistry Reference
Ethanone, 1-(4-ethylphenyl)-(937-30-4)
EPA Substance Registry System
p-Ethylacetophenone (937-30-4)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
TSCA 
TSCA listed
HS Code 
29143990

MSDS

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4-Ethylacetophenone Usage And Synthesis

Chemical Properties

clear colorless to yellow liquid

Uses

It can be used to produce 1,1'-p-phenylene-bis-ethanone. This reaction will need reagent air, cobalt naphthenate. The reaction temperature is 125°C.

Uses

Intermediates of Liquid Crystals

General Description

4-Ethylacetophenone is one of the attractive components of a carob-peanut extract that elicited a positive behavioral response from Oryzaephilus surinamensis, S. granarius and C. ferrugineus.

Synthesis

4-Ethylacetophenone is prepared from para-Ethylphenol plus Acetylchloridewith Aluminum chloride in an inert solvent (Fnedel-Craft’s reaction).

References

[1] ACS Catalysis, 2014, vol. 4, # 1, p. 321 - 327
[2] Synlett, 2016, vol. 27, # 16, p. 2378 - 2383
[3] Green Chemistry, 2015, vol. 17, # 1, p. 532 - 537
[4] Tetrahedron, 2013, vol. 69, # 19, p. 3775 - 3781
[5] Journal of Organic Chemistry, 2015, vol. 80, # 7, p. 3538 - 3546

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