ChemicalBook--->CAS DataBase List--->37593-02-5

37593-02-5

37593-02-5 Structure

37593-02-5 Structure
IdentificationMore
[Name]

4'-n-Amylacetophenone
[CAS]

37593-02-5
[Synonyms]

1-(4-PENTYL-PHENYL)ETHANONE
4-N-AMYLACETOPHENONE
4'-(N-PENTYL)ACETOPHENONE
4-N-PENTYLACETOPHENONE
4'-PENTYLACETOPHENONE
LABOTEST-BB LT00159042
P-AMYL ACETOPHENONE
P-PENTYLACETOPHENONE
TIMTEC-BB SBB007687
1-(4-pentylphenyl)-ethanon
Acetophenone, 4'-pentyl-
Ethanone, 1-(4-pentylphenyl)-
p-n-Pentylacetophenone
4'-(N-PENTYL)ACETOPHENONE 98+%
4'-AmylAcetophenone
1-(4-pentylphenyl)ethan-1-one
[Molecular Formula]

C13H18O
[MDL Number]

MFCD00043687
[Molecular Weight]

190.28
[MOL File]

37593-02-5.mol
Chemical PropertiesBack Directory
[Boiling point ]

132-133°C 4mm
[density ]

0,95 g/cm3
[refractive index ]

1.5140 to 1.5160
[Fp ]

132-133°C/4mm
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

clear liquid
[color ]

Colorless to Light yellow
[Specific Gravity]

0.95
[Usage]

Intermediates of Liquid Crystals
[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]

37593-02-5(EPA Substance)
Safety DataBack Directory
[TSCA ]

Yes
[HS Code ]

2914390090
Hazard InformationBack Directory
[Chemical Properties]

Light yellow transparent liquid
[Uses]

Intermediates of Liquid Crystals
[Synthesis]

1-Ethynyl-4-pentylbenzene

79887-10-8

4'-n-Amylacetophenone

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
Spectrum DetailBack Directory
[Spectrum Detail]

4'-n-Amylacetophenone(37593-02-5)MS
4'-n-Amylacetophenone(37593-02-5)IR1
4'-n-Amylacetophenone(37593-02-5)Raman
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

4'-n-Pentylacetophenone, 98%(37593-02-5)
[TCI AMERICA]

4'-Pentylacetophenone,>95.0%(GC)(37593-02-5)
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