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(3^2S,3S)-N-(α-methylbenzyl)-β-aminobutyric acid is a chiral compound with a unique molecular structure. It is a derivative of β-aminobutyric acid (BABA), featuring an α-methylbenzyl group attached to the nitrogen atom. The compound's chirality arises from the presence of two chiral centers, resulting in four possible stereoisomers. The specific configuration mentioned, (3^2S,3S), indicates that both chiral centers have the S (sine) configuration. (32S,3S)-N-(α-methylbenzyl)-β-aminobutyric acid has potential applications in pharmaceuticals and chemical research due to its unique properties and reactivity.

3775-71-1

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3775-71-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3775-71-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,7 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3775-71:
(6*3)+(5*7)+(4*7)+(3*5)+(2*7)+(1*1)=111
111 % 10 = 1
So 3775-71-1 is a valid CAS Registry Number.

3775-71-1Relevant academic research and scientific papers

Evaluating β-amino acids as enantioselective organocatalysts of the Hajos-Parrish-Eder-Sauer-Wiechert reaction

Davies, Stephen G.,Russell, Angela J.,Sheppard, Ruth L.,Smith, Andrew D.,Thomson, James E.

, p. 3190 - 3200 (2008/03/14)

A systematic study of the effect of substitution within the β-amino acid framework indicates that both β2- and β3- amino acids catalyse the Hajos-Parrish-Eder-Sauer-Wiechert reaction with poor to reasonable levels of enantioselectivity. These results led to the evaluation of the conformationally constrained β-amino acid (1R,2S)-cispentacin, which catalyses the Hajos-Parrish-Eder-Sauer-Wiechert reaction with comparable or higher levels of enantioselectivity to l-proline. The Royal Society of Chemistry.

Synthesis and Stereochemistry of Chiral Azetidin-2-ones and Azetidine-2-thiones. I. Synthesis of Diastereomeric 2- and 3-Substituted N-(α-Methylbenzyl)-β-aminopropionic Acids

Romanova, N. N.,Tallo, T. G.,Bundel', Yu. G.

, p. 375 - 377 (2007/10/03)

Nucleophilic addition of α-methylbenzylamine to the double bond of 2- and 3-substituted acrylic acids in pyridine under reflux proceeds nonstereoselectively.

STEREOCHEMISTRY OF THE METHYLATION OF THE (11S,4S) AND (11S,4R) DIASTEREOMERS OF 4-METHYL-1-(α-METHYLBENZYL)AZETIDIN-2-ONE

Romanova, N. N.,Tallo, T. G.,Borisenko, A. A.,Bundel', Yu. G.

, p. 761 - 766 (2007/10/02)

The methylation of the lithium derivatives of the (11S,4S) and (11S,4R) diastereomers of 4-methyl-1-(α-methylbenzyl)azetidin-2-one proceeds stereospecifically with the formation of only trans-(3S,4S)- and trans-(3R,4R)-dimethyl-1-(S

ASYMMETRIC SYNTHESIS WITH CHIRAL HYDROXYLAMINES. SYNTHESIS OF OPTICALLY PURE 4-SUBSTITUTED AZETIDINONES

Baldwin, S. W.,Aube, J.

, p. 179 - 182 (2007/10/02)

The reaction between β-substituted acrylate esters and α-methylbenzyl hydroxyl amine affords diastereoisomeric 5-isoxazolidinones, convenient precursors of simple optically pure 2-azetidinones.

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