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{[(E)-Benzyloxycarbonylimino]-[(2S,3R,4S,6R)-4-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-3-methyl-6-(2-oxo-propyl)-piperidin-1-yl]-methyl}-carbamic acid benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

269715-89-1

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  • {[(E)-Benzyloxycarbonylimino]-[(2S,3R,4S,6R)-4-(tert-butyl-dimethyl-silanyloxy)-2-(tert-butyl-dimethyl-silanyloxymethyl)-3-methyl-6-(2-oxo-propyl)-piperidin-1-yl]-methyl}-carbamic acid benzyl ester

    Cas No: 269715-89-1

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269715-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 269715-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,9,7,1 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 269715-89:
(8*2)+(7*6)+(6*9)+(5*7)+(4*1)+(3*5)+(2*8)+(1*9)=191
191 % 10 = 1
So 269715-89-1 is a valid CAS Registry Number.

269715-89-1Relevant articles and documents

Stereoselective synthesis of a tricyclic guanidinium model of cylindrospermopsin

McAlpine, Indrawan J.,Armstrong, Robert W.

, p. 1849 - 1853 (2007/10/03)

An 11-step enantioselective synthesis of the A-ring of cylindrospermopsin is described using an intramolecular conjugate addition as the key step to forming the piperidine ring. Further elaboration generates a tricyclic guanidine via a sequential double displacement strategy as a model for the cylindrospermopsin guanidinium core. (C) 2000 Elsevier Science Ltd.

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