51451-26-4

Basic information

• Product Name: 1-Propanone, 1-(2-hydroxy-6-methylphenyl)-
• CAS NO: 51451-26-4
• Molecular Formula: C10H12O2
• Molecular Weight: 164.204
• Mol File: 51451-26-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 1-(2-hydroxy-6-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 1-(2-hydroxy-6-methylphenyl)-(51451-26-4)
• EPA Substance Registry System: 1-Propanone, 1-(2-hydroxy-6-methylphenyl)-(51451-26-4)

Safety Data

• Hazardous Substances Data: 51451-26-4(Hazardous Substances Data)

Usage

Physical state

Colorless or pale yellow liquid

Odor

Sweet, floral

Uses

Production of fragrances and flavors, found in cosmetic and personal care products

Pharmaceutical and medicinal applications

Antioxidant and anti-inflammatory properties.

Upstream product

• 41389-11-1 2-allyl-3-hydroxymethylbenzene 
• 121194-61-4 2'-Hydroxy-3'-isopropyl-6'-methylpropiophenone 
• 137937-37-2 1-(2-methoxy-6-methylphenyl)-1-propanone 
• 7501-14-6 propionic acid-(2-tert-butyl-5-methyl-phenyl ester) 
• 51451-25-3 2-Propionyl-3-methyl-4-tert.-butylphenol 
• 137937-38-3 1-<3-(1,1-dimethylethyl)-2-hydroxy-6-methylphenyl>-1-propanone 

Downstream Products

• 567-61-3 2-hydroxy-6-methylbenzoic acid 
• 2886-52-4 1-(2-hydroxy-4-methyl-phenyl)-propan-1-one 
• 938-45-4 2-propionyl-p-cresol 
• 861619-09-2 3,5-dibromo-2-hydroxy-6-methyl-benzoic acid 
• 137937-37-2 1-(2-methoxy-6-methylphenyl)-1-propanone 

Relevant articles and documents

A REEXAMINATION OF THE RETRO-FRIES REARRANGEMENT OF SOME o-HYDROXYKETONES

The retro-Fries rearrangement, catalyzed by protic and Lewis acids, was studied for some o-hydroxyketones.The results are consistent with the mechanism of an heterolytic cleavage and rearrangement.It appears that, in general, Lewis acids do not induce the retro-Fries rearrangement of o-hydroxyketones.However, in certain cases, it may be brought about the presence of a protic acid generated in situ, from a solvent-catalyst interaction.

Ein neues Darstellungsverfahren fuer o-Hydroxy-propiophenone durch Reaktion von o-Allyl-phenolen mit Perbenzoesaeure

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