56010-63-0

Basic information

• Product Name: 1-Propanone, 3-hydroxy-2,2-dimethyl-1-phenyl-
• CAS NO: 56010-63-0
• Molecular Formula: C11H14O2
• Molecular Weight: 178.231
• Mol File: 56010-63-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 3-hydroxy-2,2-dimethyl-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 3-hydroxy-2,2-dimethyl-1-phenyl-(56010-63-0)
• EPA Substance Registry System: 1-Propanone, 3-hydroxy-2,2-dimethyl-1-phenyl-(56010-63-0)

Safety Data

• Hazardous Substances Data: 56010-63-0(Hazardous Substances Data)

Upstream product

• 1750-74-9 2-benzoyl-2-methylpropanal 
• 100-52-7 benzaldehyde 
• 67-56-1 methanol 
• 611-70-1 phenyl isopropyl ketone 
• 33950-46-8 1-phenyl-2,2-dimethyl-1,3-propanediol 
• 24290-47-9 1-(phenyl)-2-(methyl)-1-propylamine hydrochloride 
• 67-68-5 dimethyl sulfoxide 
• 50-00-0 formaldehyd 
• 58908-50-2 3-acetoxy-2,2-dimethylpropionyl chloride 
• 38111-44-3 phenylzinc(II) bromide 

Downstream Products

• 26921-44-8 (1-methylcyclopropyl)phenylketone 
• 15429-30-8 3-bromo-2,2-dimethyl-1-phenyl-propan-1-one 
• 100127-54-6 3-iodo-2,2-dimethyl-1-phenyl-propan-1-one 
• 101734-77-4 2,2-dimethyl-3-(4-nitro-benzoyloxy)-1-phenyl-propan-1-one 
• 50-00-0 formaldehyd 
• 611-70-1 phenyl isopropyl ketone 
• 1415476-02-6 2,2-dimethyl-1-phenyl-3-((3,3,3-trifluoroprop-1-en-2-yl)oxy)propan-1-one 
• 1372861-85-2 (S)-2,2-dimethyl-1-phenyl-1,3-propanediol 3-O-pivaloate 
• 1273614-88-2 (S)-2,2-dimethyl-1-phenyl-1,3-propanediol 3-O-benzoate 
• 98674-79-4 (S)-(+)-1-phenyl-2,2-dimethyl-1,3-propanediol 
• 130857-26-0 (S)-2,2-dimethyl-1-phenylpropane-1,3-diol 
• 128419-49-8 N-(2,2-dimethyl-1-phenyl-1-cyclopropyl)trifluoroacetamide 
• 109296-31-3 N-(benzylidene)-2,2-dimethyl-1-phenylcyclopropylamine 
• 109296-40-4 2,2-dimethyl-1-phenylcyclopropylamine 

Relevant articles and documents

Phosphinous Acid Platinum Complex as Robust Catalyst for Oxidation: Comparison with Palladium and Mechanistic Investigations

Secondary phosphine oxides proved to be effective preligands to stabilise a hydroxy-platinum based catalyst that allows the aerobic/anaerobic oxidation of challenging substrates. Kinetic comparisons showed that this system is more efficient and stable than previously reported similar palladium-based catalysts. A neutral platinum dimer bearing bridging hydroxy ligands has been isolated and fully characterised by X-ray diffraction and its involvement in the mechanism has been evidenced by mechanistic studies.

Selective aldehyde reduction in ketoaldehydes with NaBH4-Na 2CO3-H2O at room temperatures

A variety of aliphatic and aromatic ketoaldehydes were reduced to the corresponding ketoalcohols with a mixture of sodium borohydride (1.2 equivalents) and sodium carbonate (sixfold molar excess) in water. Reactions were performed at room temperatures(typically) 2 h, and yields of isolated products generally ranged from 70% to 85%. A bis-carbonate-borane complex, [(BH3)2CO2]2- 2Na+, possibly formed from the reagent mixture, is likely the active reductant. The moderated reactivity of this acylborane species would explain the chemoselectivity observed in the reactions. The readily available reagents and the mild aqueous conditions make for ease of operation and environmental compatibility, and make a useful addition to available methodology. Copyright

CHEMOSELECTIVE REDUCTION OF ALDEHYDES WITH ZINC BOROHYDRIDE IN TETRAHYDROFURAN

A variety of structurally different aldehydes undergo chemoselective reduction over ketones with zinc borohydride in tetrahydrofuran at -10 deg C to the corresponding alcohols.