Basic information Safety Supplier Related

4'-n-Amylacetophenone

Basic information Safety Supplier Related

4'-n-Amylacetophenone Basic information

Product Name:
4'-n-Amylacetophenone
Synonyms:
  • 1-(4-pentylphenyl)-ethanon
  • Acetophenone, 4'-pentyl-
  • Ethanone, 1-(4-pentylphenyl)-
  • p-n-Pentylacetophenone
  • P-AMYL ACETOPHENONE
  • P-PENTYLACETOPHENONE
  • TIMTEC-BB SBB007687
  • 1-(4-PENTYL-PHENYL)ETHANONE
CAS:
37593-02-5
MF:
C13H18O
MW:
190.28
Product Categories:
  • Acetophenones (Building Blocks for Liquid Crystals)
  • Building Blocks for Liquid Crystals
  • Functional Materials
  • bc0001
Mol File:
37593-02-5.mol
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4'-n-Amylacetophenone Chemical Properties

Boiling point:
132-133°C 4mm
Density 
0,95 g/cm3
refractive index 
1.5140 to 1.5160
Flash point:
132-133°C/4mm
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
color 
Colorless to Light yellow
Specific Gravity
0.95
InChI
InChI=1S/C13H18O/c1-3-4-5-6-12-7-9-13(10-8-12)11(2)14/h7-10H,3-6H2,1-2H3
InChIKey
KBKGPMDADJLBEM-UHFFFAOYSA-N
SMILES
C(=O)(C1=CC=C(CCCCC)C=C1)C
CAS DataBase Reference
37593-02-5(CAS DataBase Reference)
NIST Chemistry Reference
p-Pentylacetophenone(37593-02-5)
EPA Substance Registry System
Ethanone, 1-(4-pentylphenyl)- (37593-02-5)
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Safety Information

TSCA 
Yes
HS Code 
2914390090

MSDS

  • Language:English Provider:ALFA
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4'-n-Amylacetophenone Usage And Synthesis

Chemical Properties

Light yellow transparent liquid

Uses

Intermediates of Liquid Crystals

Synthesis

79887-10-8

37593-02-5

GENERAL PROCEDURE: The reaction was carried out in a magnetically stirred circular three-necked flask equipped with a condenser, which was placed in a thermostatic oil bath. To a well stirred mixed solution of 4-pentylphenylacetylene (2 mmol) and H2O (8 mmol) was added zeolite (H-type, 100 mg) and the reaction mixture was stirred and reacted at 100 °C. The reaction progress was monitored by TLC and after complete disappearance of 4-pentylphenylacetylene or for a predetermined time, the reaction mixture was cooled to room temperature and diluted with ethyl acetate. The catalyst was separated by filtration and the solvent was subsequently evaporated under reduced pressure to give the crude product. The crude product was further purified by silica gel column chromatography (100-200 mesh) to give pure p-pentyl acetophenone. The structures of all the products were confirmed by 1H NMR and 13C NMR spectral data.

References

[1] Applied Catalysis A: General, 2015, vol. 505, p. 213 - 216
[2] European Journal of Organic Chemistry, 2018, vol. 2018, # 29, p. 3974 - 3981
[3] Tetrahedron Letters, 2013, vol. 54, # 33, p. 4414 - 4417
[4] Catalysis Communications, 2015, vol. 65, p. 102 - 104
[5] Applied Organometallic Chemistry, 2012, vol. 26, # 12, p. 722 - 726

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