5650-41-9

Basic information

• Product Name: 3'-HYDROXYPROPIOPHENONE
• Synonyms: 2-benzoylethanol;m-Hydroxypropiophenone;3-hydroxy-1-phenylpropan-1-one;1-Propanone, 3-hydroxy-1-pheny;1-Propanone, 3-hydroxy-1-phenyl
• CAS NO: 5650-41-9
• Molecular Formula: C₉H₁₀O₂
• Molecular Weight: 150.17
• Mol File: 5650-41-9.mol
• Article Data: 80

Chemical Properties

• Melting Point: 24°C
• Boiling Point: 231.72°C (rough estimate)
• Appearance: /
• Density: 1.1078
• Refractive Index: 1.5450 (estimate)
• PKA: 14.37±0.10(Predicted)
• CAS DataBase Reference: 3'-HYDROXYPROPIOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3'-HYDROXYPROPIOPHENONE(5650-41-9)
• EPA Substance Registry System: 3'-HYDROXYPROPIOPHENONE(5650-41-9)

Safety Data

• Hazardous Substances Data: 5650-41-9(Hazardous Substances Data)

Upstream product

• 590-92-1 3-Bromopropionic acid 
• 7334-41-0 3-acetoxypropiophenone 
• 26029-34-5 2-methyl-3-phenyl-2-cyclopentenone 
• 1504-58-1 3-Phenyl-2-propyn-1-ol 
• 1600-27-7 mercury(II) diacetate 
• 50-00-0 formaldehyd 
• 536-74-3 phenylacetylene 
• 71-43-2 benzene 
• 29526-96-3 1-phenylcyclopropan-1-ol 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 67-56-1 methanol 
• 84965-95-7 4-hexyl-3-phenyl-4,5-dihydroisoxazole 
• 5650-34-0 2,3-epoxy-1-phenylpropan-1-one 
• 14397-33-2 3-phenyl-2-isoxazoline 

Downstream Products

• 768-03-6 Phenyl vinyl ketone 
• 2538-52-5 1,3-diphenyl-4,5-dihydro-1H-pyrazole 
• 92567-73-2 (tetrahydropyrannyloxy-2')-3 phenyl-1 propanone-1 
• 92567-74-3 phenyl-1 vinyloxy-3 propanone-1 
• 56323-47-8 3-Hydroxypropiophenoncarbamat 
• 96854-34-1 (S)-3-phenyl-1,3-propanediol 
• 95700-06-4 N,N-bis-(3-hydroxyimino-3-phenyl-propyl)-hydroxylamine 
• 96170-50-2 N,N-bis-(3-oxo-3-phenyl-propyl)-hydroxylamine 
• 866269-79-6 3-oxo-2-phenylpropyl (E)-3-phenylpropenoate 
• 14593-04-5 3-amino-3-phenyl-1-propanol 
• 170564-98-4 (R)-3-amino-3-phenyl-1-propanol 
• 406468-05-1 3-[N-(phenylacetyl)amino]-3-phenyl-1-propanol 
• 881853-41-4 3-[N-(phenylacetyl)amino]-3-phenyl-1-propanol 
• 936499-93-3 (S)-3-amino-3-phenyl-1-propanol hydrochloride 

Relevant articles and documents

Porous organic polymer-supported manganese catalysts with tunable wettability for efficient oxidation of secondary alcohols

Porous organic polymers (POPs) feature high surface areas, tunable components, and designable hierarchical pores, thus showing versatile applications including catalysis, separation, gas storage and so on. However, the inherently hydrophobic property may be unfavorable for the catalytic reaction that involves hydrophilic reactants. By using the hydrophilic principle of the amide bond, R-NH-CO-R can be constructed in the porous frameworks to regulate the wettability. Herein, we report the construction of an amphiphilic and hierarchical porous Mn-N4 catalyst via the solvothermal copolymerization, in which N,N-methylenebisacrylamide is used as a hydrophilic monomer. This POP-based manganese catalyst can effectively promote the oxidation of secondary alcohol to produce the ketone using aqueous hydrogen peroxide as the oxidant under mild conditions. Note that this amphiphilic catalyst displays high catalytic activity as its homogeneous counterpart in the selective oxidation of alcohols. The present work has provided a successful approach for improving the catalytic activity by tuning the wettability of POP-based heterogeneous catalysts.

Catalytic Net Oxidative C-C Activation and Silylation of Cyclopropanols with a Traceless Acetal Directing Group

Redox-neutral carbon-carbon (C-C) bond activation and functionalization strategies of cyclopropanols that give metallo homoenolate have offered merits to construct a range of useful β-functionalized ketones in an inverse-polarity fashion. Discovery and id

LIGHT INDUCED CATALYTIC C-H OXYGENATION OF ALKANES

A method of oxygenating a benzylic C-H bond is provided. The method comprises light induced activation of an initiator and subsequent reaction with oxygen, resulting in the formation of free radicals. Subsequently, free radicals catalyze the reaction of the benzylic C-H bond with oxygen, thereby forming an oxygenated compound.