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(2S,3S)-2-{(S)-2-[(R)-1-(2,2-Dimethyl-propionylamino)-ethyl]-benzenesulfinyl}-3-hydroxy-4,4-dimethyl-pentanoic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144434-08-2

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144434-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144434-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,3 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 144434-08:
(8*1)+(7*4)+(6*4)+(5*4)+(4*3)+(3*4)+(2*0)+(1*8)=112
112 % 10 = 2
So 144434-08-2 is a valid CAS Registry Number.

144434-08-2Downstream Products

144434-08-2Relevant academic research and scientific papers

Recoverable Chiral Sulfoxides for Asymmetric Synthesis: Preparation, Regeneration and Application to the Asymmetric Aldol Reaction

Butlin, Roger J.,Linney, Ian D.,Critcher, Douglas J.,Mahon, Mary F.,Molloy, Kieran C.,Wills, Martin

, p. 1581 - 1590 (2007/10/02)

The synthesis of a novel source of chiral sulfoxide and its application to the control of asymmetric aldol reactions is described.The sulfoxide precursor S(S)R-(+)-cis-4 may be recycled and thus affords a considerable advantage over currently a

A New Class of Recoverable Chiral Sulphoxide: Application to the Asymmetric Synthesis of β-Hydroxy Esters.

Wills, Martin,Butlin, Roger J.,Linney, Ian D.

, p. 5427 - 5430 (2007/10/02)

Enantiomerically pure cyclic sulphinamide S(S)R-(+)-2 was prepared from homochiral sulphinic acid R-(-)-1 and subsequently converted to the ester S(S)R-(-)-3 via ring opening with an ester enolate.Aldol reactions of S(S)R-

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