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Propiophenone, 99%, Thermo Scientific Chemicals
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Catalog number A15140.0E
also known as A15140-0E
Price (USD)/ Each
197.65
Online exclusive
219.00 Save 21.35 (10%)
-
Quantity:
2500 g
Price (USD)/ Each
197.65
Online exclusive
219.00 Save 21.35 (10%)
Propiophenone, 99%, Thermo Scientific Chemicals
Catalog numberA15140.0E
Price (USD)/ Each
197.65
Online exclusive
219.00 Save 21.35 (10%)
-
Chemical Identifiers
CAS93-55-0
IUPAC Name1-phenylpropan-1-one
Molecular FormulaC9H10O
InChI KeyKRIOVPPHQSLHCZ-UHFFFAOYSA-N
SMILESCCC(=O)C1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetFormLiquid
Appearance (Color)Clear colorless to yellow to brown
Assay (GC)≥98.5%
Refractive Index1.5245-1.5280 @ 20?C
Propiophenone is an intermediate in the synthesis of pharmaceuticals and organic compounds. It is used in the synthesis of ephedrine and propiophenone derivatives such as cathinone, and methcathinone. It can also be used in the synthesis of aryl alkenes.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Propiophenone is an intermediate in the synthesis of pharmaceuticals and organic compounds. It is used in the synthesis of ephedrine and propiophenone derivatives such as cathinone, and methcathinone. It can also be used in the synthesis of aryl alkenes.
Solubility
Difficult to mix.
Notes
Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
Propiophenone is an intermediate in the synthesis of pharmaceuticals and organic compounds. It is used in the synthesis of ephedrine and propiophenone derivatives such as cathinone, and methcathinone. It can also be used in the synthesis of aryl alkenes.
Solubility
Difficult to mix.
Notes
Keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only
General References:
- Shu Kobayashi.; Satoshi Nagayama. Aldehydes vs Aldimines. Unprecedented Reactivity in Their Enolate Addition Reactions. J. Org. Chem. 1997, 62, (2), 232-233.
- David P. Thomasa.; Joe P. Foley. Improved efficiency in micellar liquid chromatography using triethylamine and 1-butanol as mobile phase additives to reduce surfactant adsorption. Journal of Chromatography A. 2008, 1205, (1-2), 36-45.
- Propiophenone and its derivatives are readily rearranged to methyl esters of ɑ-methyl arylacetic acids by reaction with I2, ICl or ICl3 in trimethyl orthoformate: J. Org. Chem., 53, 4859 (1988).
- Undergoes a Mannich reaction with hexamethylenetetramine in acetic anhydride. The resulting ɑ-methylene derivative can be cyclized to an indanone in high yield: Synth. Commun., 26, 1775 (1996):