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(4S,5R,6R)-5-Acetylamino-4-tert-butoxycarbonylamino-6-((1R,2R)-1,2,3-trihydroxy-propyl)-5,6-dihydro-4H-pyran-2-carboxylic acid benzhydryl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

166830-76-8

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166830-76-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 166830-76-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,8,3 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 166830-76:
(8*1)+(7*6)+(6*6)+(5*8)+(4*3)+(3*0)+(2*7)+(1*6)=158
158 % 10 = 8
So 166830-76-8 is a valid CAS Registry Number.

166830-76-8Downstream Products

166830-76-8Relevant academic research and scientific papers

Dihydropyrancarboxamides related to zanamivir: A new series of inhibitors of influenza virus sialidases. 1. Discovery, synthesis, biological activity, and structure-activity relationships of 4-guanidino- and 4-amino-4h-pyran-6-carboxamides

Smith, Paul W.,Sollis, Steven L.,Howes, Peter D.,Cherry, Peter C.,Starkey, Lan D.,Cobley, Kevin N.,Weston, Helen,Scicinski, Jan,Merritt, Andrew,Whittington, Andrew,Wyatt, Paul,Taylor, Neil,Green, Darren,Bethell, Richard,Madar, Safia,Fenton, Robert J.,Morley, Peter J.,Pateman, Tony,Beresford, Alan

, p. 787 - 797 (2007/10/03)

4-Amino- and 4-guanidino-4ff-pyran-6-carboxamides 4 and 5 related to zanamivir (GG167) are a new class of inhibitors of influenza virus sialidases. Structure-activity studies reveal that, in general, secondary amides are weak inhibitors of both influenza

Synthesis of 6-, 7- and 8-carbon sugar analogues of potent anti-influenza 2,3-didehydro-2,3-dideoxy-N-acetylneuraminic acid derivatives

Bamford, Mark J.,Pichel, Julia Castro,Husman, Wahid,Patel, Bina,Storer, Richard,Weir, Niall G.

, p. 1181 - 1188 (2007/10/02)

Analogues of the potent anti-influenza A and B compound, 4-guanidino-Neu5Ac2en, are described in which the stereochemically demanding C-6-glycerol side-chain is truncated.Syntheses of the one- and two-carbon side-chain analogues, of both 4-guanidino- and 4-amino-Neu5Ac2en, are presented, as well as the syntheses of analogues lacking any side-chain.Whilst complete removal of the C-6 side-chain abolishes activity, a stepwise increase in inhibition of influenza neuraminidase and influenza A and B in cell culture with increasing C-6 chain length is observed.The one-carbon, hydroxymethyl derivative retains significant activity to represent a suitable lead in the search for neuraminidase inhibitors of reduced stereochemical demand and synthetic complexity.

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