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[2R,3R]-(+)-3-hydroxy-2,4,4-trimethyl-1-phenyl-1-pentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

283151-95-1

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283151-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 283151-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,3,1,5 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 283151-95:
(8*2)+(7*8)+(6*3)+(5*1)+(4*5)+(3*1)+(2*9)+(1*5)=141
141 % 10 = 1
So 283151-95-1 is a valid CAS Registry Number.

283151-95-1Downstream Products

283151-95-1Relevant academic research and scientific papers

Development of asymmetric reactions catalyzed by chiral organotin-alkoxide reagents

Yanagisawa, Akira,Yoshida, Kazuhiro

, p. 117 - 127 (2013)

Asymmetric catalysis under almost-neutral reaction conditions is key for the efficient synthesis of optically active polar molecules. We have developed catalytic enantioselective reactions of acyclic or cyclic alkenyl esters by using an (S)-BINOL-derived

Asymmetric aldol reactions using (S,S)-(+)-pseudoephedrine-based amides: Stereoselective synthesis of α-methyl-β-hydroxy acids, esters, ketones, and 1,3-syn and 1,3-anti diols

Vicario, Jose L.,Badia, Dolores,Dominguez, Esther,Rodriguez, Monica,Carrillo, Luisa

, p. 3754 - 3759 (2007/10/03)

A very efficient method for performing stereoselective aldol reactions is reported. The reaction of (S,S)-(+)-pseudoephedrine-derived propionamide enolates with several aldehydes yielded exclusively one of the four possible diastereomers in good yields, although transmetalation of the firstly generated lithium enolate with a zirconium(II) salt, prior to the addition of the aldehyde, is necessary in order to achieve high syn selectivity. The so-formed syn-α-methyl-β-hydroxy amides were transformed into other valuable chiral nonracemic synthons such as α-methyl-β-hydroxyacids, esters, and ketones. Finally, a stereocontrolled reduction procedure starting from the so-obtained α-methyl-β-hydroxy ketones has been developed allowing the synthesis of either 1,3-syn- or 1,3-anti-α-methyl-1,3-diols in almost enantiopure form by choosing the appropriate reaction conditions.

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