Cookies disclaimer

I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.

93-55-0 - Propiophenone, 99% - Ethyl phenyl ketone - 1-Phenyl-1-propanone - A15140 - Alfa Aesar

A15140 Propiophenone, 99%

CAS-Nummer
93-55-0
Synonyme
Ethyl phenyl ketone
1-Phenyl-1-propanone

Größe Preis ($) Menge Verfügbarkeit
100g 16,11
500g 36,72
2500g 129,60
Zum Warenkorb hinzufügen Zur Angebotsanfrage hinzufügen Artikel anzeigen

Propiophenone, 99%

MDL
MFCD00009309
EINECS
202-257-6

Chemische Eigenschaften

Formel
C9H10O
Molmasse
134.18
Schmelzpunkt
17-18°
Siedepunkt
217-218°
Flammpunkt
87°(188°F)
Dichte
1.008
Brechungsindex
1.5260
Löslichkeit
Difficult to mix.

Anwendungen

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.

Bemerkungen

Keep container tightly closed. Store in cool, dry conditions in well sealed containers.

Literaturverweise

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):

GHS Gefahren- und Sicherheitshinweise

Gefahrenhinweise (EU): H227

Combustible liquid.

Sicherheitshinweise: P210-P280-P370+P378a-P403+P235-P501a

Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Wear protective gloves/protective clothing/eye protection/face protection. In case of fire: Use for extinction: CO2, powder or water spray. Store in a well-ventilated place. Keep cool. Dispose of contents/container in accordance with local/regional/national/international regulations.

Weitere Referenzen

Merck
14,7830
Beilstein
606215
Harmonized Tariff Code
2914.39
TSCA
Yes
RTECS
UG7175000

Empfohlen

Kürzlich angesehen

Chemikalien

Life science

Metalle und Stoffe

Katalysatoren

Forschungs- und Laborbedarf