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(R)-3-Diphenylphosphinoyl-2-hydroxy-2-methylpropanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

165557-48-2

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165557-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 165557-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,5,5 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 165557-48:
(8*1)+(7*6)+(6*5)+(5*5)+(4*5)+(3*7)+(2*4)+(1*8)=162
162 % 10 = 2
So 165557-48-2 is a valid CAS Registry Number.

165557-48-2Upstream product

165557-48-2Relevant academic research and scientific papers

Synthesis of (R)- or (S)-diphenylphosphinoyl hydroxy aldehydes and 1,2-diols using Mukaiyama's bicyclic aminal methodology and Sharpless asymmetric dihydroxylation

O'Brien, Peter,Warren, Stuart

, p. 2129 - 2138 (2007/10/03)

Two different approaches to diphenylphosphinoyl hydroxy aldehydes and 1,2-diols are compared. A lengthy chiral auxiliary approach using proline-derived aminals enables hydroxy aldehydes and 1,2-diols of known absolute stereochemistry and high enantiomeric

Stereocontrolled Synthesis of R or S Diphenylphosphinoyl Hydroxy Aldehydes and 1,2-Diols Using Bicyclic Aminals

O'Brien, Peter,Warren, Stuart

, p. 2681 - 2684 (2007/10/02)

Homochiral diphenylphosphinoyl hydroxy aldehydes 1 and 2 have been made by diastereoselective additions of metallated methyldiphenylphosphine oxides 10 to Mukaiyama's keto aminals 8 and 9.Reduction to diphenylphosphinoyl 1,2 diols 3 and 4 is also described.Sharpless asymmetric dihydroxylation provides an alternative route diphenylphosphinoyl 1,2 diols 3 and 4, the two approaches are compared.

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