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Benzenesulfonamide, N-[(1R)-1-[[2-[(2R,5S)-2,5-bis[[(1,1-dimethylethyl)dimethylsilyl]oxy]nonyl] -1,3-dithian-2-yl]methyl]butyl]-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

692730-44-2

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692730-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 692730-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,2,7,3 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 692730-44:
(8*6)+(7*9)+(6*2)+(5*7)+(4*3)+(3*0)+(2*4)+(1*4)=182
182 % 10 = 2
So 692730-44-2 is a valid CAS Registry Number.

692730-44-2Relevant academic research and scientific papers

A general, convergent strategy for the construction of indolizidine alkaloids: Total syntheses of (-)-indolizidine 223AB and alkaloid (-)-205B

Smith III, Amos B.,Kim, Dae-Shik

, p. 2547 - 2557 (2007/10/03)

N-Toluenesulfonyl aziridines comprise effective second electrophiles in the solvent controlled three-component linchpin union of silyl dithianes for the stereocontrolled convergent elaboration of protected 1,5-amino alcohols. This tactic, in conjunction w

Multicomponent linchpin coupling of silyl dithianes employing an N-Ts aziridine as the second electrophile: Synthesis of (-)-indolizidine 223AB

Smith III, Amos B.,Kim, Dae-Shik

, p. 1493 - 1495 (2007/10/03)

An efficient, stereocontrolled assembly of the indolizidine alkaloid, (-)-indolizidine 223AB, exploiting a three-component linchpin coupling employing an N-Ts aziridine as the second electrophile, followed by a one-pot sequential construction of the indol

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