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3-Hydroxy-2-methyl-1-phenyl-4-penten-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79314-56-0

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79314-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79314-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,1 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79314-56:
(7*7)+(6*9)+(5*3)+(4*1)+(3*4)+(2*5)+(1*6)=150
150 % 10 = 0
So 79314-56-0 is a valid CAS Registry Number.

79314-56-0Relevant academic research and scientific papers

Lanthanide Triflates as Water-Tolerant Lewis Acids. Activation of Commercial Formaldehyde Solution and Use in the Aldol Reaction of Silyl Enol Ethers with Aldehydes in Aqueous Media

Kobayashi, Shu,Hachiya, Iwao

, p. 3590 - 3596 (1994)

Lanthanide trifluoromethanesulfonates (triflates), especially ytterbium triflate (Yb(OTf)3), were found to be stable Lewis acids in water.In the presence of a catalytic amount of lanthanide triflate, formaldehyde in water solution (commercial formaldehyde

Iron(III) chloride as a water-compatible lewis acid for diastereoselective aldol reactions in water in the presence of a surfactant

Aoyama, Naohiro,Manabe, Kei,Kobayashi, Shu

, p. 312 - 313 (2007/10/03)

Diastereoselective aldol reactions of various aldehydes with silicon enolates in water have been successfully carried out using iron(III) chloride and a surfactant. Contrary to previous understanding, iron(III) chloride has been shown to be a water-compat

Rare Earth Metal Complexes as Water-Tolerant Lewis Acid Catalysts in Organic Synthesis

Kobayashi,Hashiya,Ishitani,Moriwaki,Nagayama

, p. 193 - 202 (2007/10/03)

Rare earth metal triflates are stable in aqueous media and can act as Lewis acid catalysts in several carbon-carbon bond forming reactions. This article describes some of these reactions; aldol and Mannich-type reactions in aqueous solution, and Friedel-Crafts acylations and Fries rearrangement in organic solvents. The reactions proceeded smoothly in the presence of a catalytic amount of the triflate under mild conditions. Moreover, the catalysts could be recovered after the reactions were completed and could be reused.

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