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540641

Sigma-Aldrich

4′-Butoxyacetophenone

97%

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About This Item

Linear Formula:
CH3(CH2)3OC6H4COCH3
CAS Number:
Molecular Weight:
192.25
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.531 (lit.)

bp

302-304 °C (lit.)

density

1.017 g/mL at 25 °C (lit.)

SMILES string

CCCCOc1ccc(cc1)C(C)=O

InChI

1S/C12H16O2/c1-3-4-9-14-12-7-5-11(6-8-12)10(2)13/h5-8H,3-4,9H2,1-2H3

InChI key

YYLCJWIQUFHYMY-UHFFFAOYSA-N

General description

4′-Butoxyacetophenone is a mildly electron-enriched phenylmethylketone.

Application

4′-Butoxyacetophenone (4-Butoxyacetophenone) may be used to synthesize:
  • 3,5-di-(4-butoxyphenyl)-1H-pyrazole
  • (E)-1-(4-butoxyphenyl)-3-phenylprop-2-en-1-one
  • 5-aryl-6H-1,3,4-thiadiazine

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Multinuclear NMR study of Au (I), Pd (II) and Ag (I) pyrazole complexes to investigate the coordination mode.
Cornago P, et al.
ARKIVOC (Gainesville, FL, United States), 9, 21-29 (2005)
NIR optical carbon dioxide sensors based on highly photostable dihydroxy-aza-BODIPY dyes.
Schutting S, et al.
Journal of Material Chemistry C, 3(21), 5474-5483 (2015)
A Versatile One-Pot Procedure for the Synthesis of 5-Aryl-6H-1, 3, 4-thiadiazine-2-amines from Aromatic Ketones.
Hartmann R, et al.
Synlett, 27(6), 864-867 (2016)

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