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methyl (2R,3S,4S)-2,4-dimethyl-3-hydroxy-5-(4-methoxybenzyloxy)pentanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

496035-49-5

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496035-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 496035-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,6,0,3 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 496035-49:
(8*4)+(7*9)+(6*6)+(5*0)+(4*3)+(3*5)+(2*4)+(1*9)=175
175 % 10 = 5
So 496035-49-5 is a valid CAS Registry Number.

496035-49-5Relevant academic research and scientific papers

A second-generation total synthesis of (+)-discodermolide: The development of a practical route using solely substrate-based stereocontrol

Paterson, Ian,Delgado, Oscar,Florence, Gordon J.,Lyothier, Isabelle,O'Brien, Matthew,Scott, Jeremy P.,Sereinig, Natascha

, p. 150 - 160 (2007/10/03)

(Chemical Equation Presented). A novel total synthesis of the complex polyketide (+)-discodermolide, a promising anticancer agent of sponge origin, has been completed in 7.8% overall yield over 24 linear steps, with 35 steps altogether. This second-genera

SYNTHESIS OF DISCODERMOLIDE

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Page 75, (2010/11/30)

The invention relates to a process for preparing discodermolide, for preparing intermediates for the manufacture of discodermolide and discodermolide analogues and to the intermediates obtained during the process. Wherein the process proceeds via a tetrae

1,6-asymmetric induction in boron-mediated aldol reactions: application to a practical total synthesis of (+)-discodermolide.

Paterson, Ian,Delgado, Oscar,Florence, Gordon J,Lyothier, Isabelle,Scott, Jeremy P,Sereinig, Natascha

, p. 35 - 38 (2007/10/03)

By relying solely on substrate-based stereocontrol, a practical total synthesis of the microtubule-stabilizing anticancer agent (+)-discodermolide has been realized. This exploits a novel aldol bond construction with 1,6-stereoinduction from the boron eno

Expeditious synthesis of a key C9-C21 subunit of the aplysiatoxins and oscillatoxins

Walkup,Kane,Boatman Jr.,Cunningham

, p. 7587 - 7590 (2007/10/02)

The C9-C21 portion of the aplysiatoxin/oscillatoxin bluegreen algal metabolites was synthesized as the 9-aldehyde bearing a tert-butyldimethylsilyl ether group on the C11 hydroxyl and a trimethylsilylethoxymethyl ether gro

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