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(R,R)-2-benzyl-3,4-dimethylisoxazolidin-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

613672-40-5

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613672-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 613672-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,3,6,7 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 613672-40:
(8*6)+(7*1)+(6*3)+(5*6)+(4*7)+(3*2)+(2*4)+(1*0)=145
145 % 10 = 5
So 613672-40-5 is a valid CAS Registry Number.

613672-40-5Relevant academic research and scientific papers

BETA-AMINO ACIDS AND METHODS AND INTERMEDIATES FOR MAKING SAME

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Page/Page column 11-12; 14-15, (2011/10/02)

Disclosed are β-amino acids that are unsubstituted in the β position; that are substituted in the β position with an aryl group; that are substituted in the α position with an aryl group; that bear two substituents in the α position; and/or that are substituted in the α and β positions with groups which, together with the carbon atoms at the α and β positions, form a ring. Also disclosed are methods for making the above-mentioned β-amino acids and other β-amino acids which involve providing an α,β-unsaturated imide; converting the α,β-unsaturated imide to a 2-substituted-isoxazolidin-5-one; and converting the 2-substituted-isoxazolidin-5-one to a β-amino acid.

Enantioselective synthesis of α,β-disubstituted-β-amino acids

Sibi, Mukund P.,Prabagaran, Narayanasamy,Ghorpade, Sandeep G.,Jasperse, Craig P.

, p. 11796 - 11797 (2007/10/03)

Highly diastereoselective and enantioselective addition of N-benzylhydroxylamine to imides 17 and 20-30 produces α,β-trans-disubstituted N-benzylisoxazolidinones 19 and 31-41. These reactions proceed in 60-96% ee with 93-99% de's using 5 mol % of Mg(NTf2)2 and ligand 18. The product isoxazolidinones can be hydrogenolyzed directly to provide ∞,β-disubstituted-β-amino acids. Copyright

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