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(S)-(+)-N-((2E)-3-phenylprop-2-enylidene)-p-toluenesulfinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

153277-52-2

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153277-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153277-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,2,7 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 153277-52:
(8*1)+(7*5)+(6*3)+(5*2)+(4*7)+(3*7)+(2*5)+(1*2)=132
132 % 10 = 2
So 153277-52-2 is a valid CAS Registry Number.

153277-52-2Relevant academic research and scientific papers

Stereoselective synthesis of β-amino acid derivatives by asymmetric mannich reaction in flow

Yoshida, Masahito,Umeda, Koji,Doi, Takayuki

, p. 1157 - 1163 (2017/10/25)

A continuous flow synthesis of β-amino acid derivatives has been demonstrated using an asymmetric Mannich reaction. An enolate of tert-butyl acetate was successfully prepared in 10s at room temperature in a flow reactor, and the desired β-amino acid derivatives were stereoselectively obtained within a short residence time (40 s) in moderate-to-good yields. Sequential Nalkylation of the Mannich product in the flow reactor was also achieved in the presence of DMPU that provided N-alkylated β-amino acid derivatives in good yields.

Synthesis of highly functionalized pyrrolidines via a selective iodide-mediated ring expansion of methylenecyclopropyl amides

Scott, Mark E.,Lautens, Mark

supporting information; experimental part, p. 8154 - 8162 (2009/04/04)

(Chemical Equation Presented) This manuscript describes a highly selective iodide-mediated, tandem Mannich/cyclization to afford trans-2,3-disubstituted pyrrolidines from methylenecyclopropyl amides in good to excellent yields and selectivities. The reaction scope has been drastically expanded to include a wide array of aromatic, heteroaromatic and α,β-unsaturated imines, as well as a variety of methylenecyclopropyl amides. Additionally, mechanistic studies were carried out to ascertain the nature of the ring-opening/ring- closing mechanism using deuterated substrates. Results from these studies indicate that the primary mechanism is an SN2/SN2 ring opening/ring closing and that iodine- or iodide-mediated isomerization of the iodo enolate is likely occurring.

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