62894-04-6

Basic information

• Product Name: 3-Buten-1-one, 2,2-dimethyl-1-phenyl-
• Synonyms: 2,2-dimethyl-1-phenyl-3-buten-1-one;3-Buten-1-one,2,2-dimethyl-1-phenyl;2,2-dimethyl-1-phenyl-3-butene-1-one;phenyl prenyl ketone
• CAS NO: 62894-04-6
• Molecular Formula: C12H14O
• Molecular Weight: 174.243
• Mol File: 62894-04-6.mol
• Article Data: 27

Chemical Properties

• Boiling Point: 59-61 °C(Press: 0.1 Torr)
• Density: 0.956±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 3-Buten-1-one, 2,2-dimethyl-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Buten-1-one, 2,2-dimethyl-1-phenyl-(62894-04-6)
• EPA Substance Registry System: 3-Buten-1-one, 2,2-dimethyl-1-phenyl-(62894-04-6)

Safety Data

• Hazardous Substances Data: 62894-04-6(Hazardous Substances Data)

Upstream product

• 65755-93-3 5-methyl-2-phenyl-2-(trimethylsiloxy)-4-hexenal 
• 65755-94-4 3,3-dimethyl-2-phenyl-2-(trimethylsiloxy)-4-pentenal 
• 98-88-4 benzoyl chloride 
• 503-60-6 3,3-dimethyl-allyl chloride 
• 100-47-0 benzonitrile 
• 870-63-3 prenyl bromide 
• 177859-18-6 1-[(3-Methyl-but-2-enyloxy)-phenyl-methyl]-1H-benzotriazole 
• 93-97-0 benzoic acid anhydride 
• 39158-85-5 2-methyl-1-phenyl-1-trimethylsiloxy-1-propene 
• 1066-54-2 trimethylsilylacetylene 
• 100-52-7 benzaldehyde 
• 613-90-1 benzoyl cyanide 
• 27644-02-6 2,2-dimethyl-1-phenylbut-3-en-1-ol 
• 115-18-4 2-methyl-3-buten-2-ol 

Downstream Products

• 1221447-21-7 (E)-2,2-dimethyl-1-phenylbut-3-en-1-one oxime 

Relevant articles and documents

New electrochemical preparation of reactive zinc with a large surface area

Reactive zinc was readily prepared by electrolysis of a DMF solution containing 0.1M Et4NClO4 using a platinum cathode and a zinc anode. Characterization of the zinc metal showed that it was an aggregation of very line, crystalline z

Trifluoromethylthiolation and trifluoromethanesulfonylation of β,γ-unsaturated hydrazones

The trifluoromethylthiolation and trifluoromethanesulfonylation of β,γ-unsaturated hydrazones was accomplished with silver(I) trifluoromethanethiolate (AgSCF3) as a CF3S source and sodium trifluoromethylsulfinate (CF3SO2Na) as a CF3SO2 source, respectively. These general methods for the preparation of dihydropyrazoles containing CF3S or CF3SO2 groups were characterized by mild reaction conditions and good functional group tolerance.

Copper-Catalyzed Diamination of Alkenes of Unsaturated Ketohydrazones with Amines

A convenient copper-catalyzed intra-/intermolecular diamination of β,γ-unsaturated hydrazones has been developed with simple amines as external amine sources. The protocol enables efficient access to various nitrogen-containing pyrazolines under mild reaction conditions.