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(2S)-2-benzyl-N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-N,2-dimethylbutanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1068601-18-2

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1068601-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1068601-18-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,8,6,0 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1068601-18:
(9*1)+(8*0)+(7*6)+(6*8)+(5*6)+(4*0)+(3*1)+(2*1)+(1*8)=142
142 % 10 = 2
So 1068601-18-2 is a valid CAS Registry Number.

1068601-18-2Downstream Products

1068601-18-2Relevant academic research and scientific papers

Pseudoephenamine: A practical chiral auxiliary for asymmetric synthesis

Morales, Marvin R.,Mellem, Kevin T.,Myers, Andrew G.

supporting information; experimental part, p. 4568 - 4571 (2012/06/30)

Unrestricted: Pseudoephenamine is introduced as a versatile chiral auxiliary and an alternative to pseudoephedrine in asymmetric synthesis. It is free from regulatory restrictions and leads to remarkable stereocontrol in alkylation reactions, especially in those that form quaternary carbon centers. Amides derived from pseudoephenamine exhibit a high propensity to be crystalline substances, and provide sharp, well-defined signals in NMR spectra. Copyright

Stereocontrolled alkylative construction of quaternary carbon centers

Kummer, David A.,Chain, William J.,Morales, Marvin R.,Quiroga, Olga,Myers, Andrew G.

supporting information; experimental part, p. 13231 - 13233 (2009/02/06)

Protocols for the stereodefined formation of α,α-disubstituted enolates of pseudoephedrine amides are presented followed by the implementation of these in diastereoselective alkylation reactions. Direct alkylation of α,α-disubstituted pseudoephedrine amide substrates is demonstrated to be both efficient and diastereoselective across a range of substrates, as exemplified by alkylation of the diastereomeric pseudoephedrine α-methylbutyramides, where both substrates are found to undergo stereospecific replacement of the α-C-H bond with α-C-alkyl, with retention of stereochemistry. This is shown to arise by sequential stereospecific enolization and alkylation reactions, with the alkyl halide attacking a common π-face of the E- and Z-enolates, proposed to be opposite the pseudoephedrine alkoxide side chain. Pseudoephedrine α-phenylbutyramides are found to undergo highly stereoselective but not stereospecific α-alkylation reactions, which evidence suggests is due to facile enolate isomerization. Also, we show that α,α-disubstituted pseudoephedrine amide enolates can be generated in a highly stereocontrolled fashion by conjugate addition of an alkyllithium reagent to the s-cis-conformer of an α-alkyl-α,β-unsaturated pseudoephedrine amide, providing α,α-disubstituted enolate substrates that undergo alkylation in the same sense as those formed by direct deprotonation. Methods are presented to transform the α-quaternary pseudoephedrine amide products into optically active carboxylic acids, ketones, primary alcohols, and aldehydes. Copyright

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