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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
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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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Find documentation for the products that you have recently purchased in the Document Library.
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)
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)
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