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(7S)-7-C-((2R,4S,5E,8R,10S,12R,14S,15E,18S,19E,22R)-25-{[(allyloxy)carbonyl]amino}-2,10,12,14,18,22-hexakis{[tert-butyl(dimethyl)silyl]oxy}-4,8-dihydroxypentacosa-5,15,19-trien-1-yl)-3-O-[tert-butyl(dimethyl)silyl]-2,4,6-trideoxy-1-O-(3,4-dimethoxybenzyl)-4-methyl-5,7-O-(oxomethylene)-D-xylo-heptitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1428672-06-3

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1428672-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428672-06-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,6,7 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1428672-06:
(9*1)+(8*4)+(7*2)+(6*8)+(5*6)+(4*7)+(3*2)+(2*0)+(1*6)=173
173 % 10 = 3
So 1428672-06-3 is a valid CAS Registry Number.

1428672-06-3Downstream Products

1428672-06-3Relevant academic research and scientific papers

Enantio- and diastereoselective synthesis of N-acetyl dihydrotetrafibricin methyl ester

Nuhant, Philippe,Roush, William R.

supporting information, p. 5340 - 5343 (2013/05/22)

A highly diastereoselective synthesis of N-acetyl dihydrotetrafibricin methyl ester (34) is described. The synthesis features three enantioselective double allylboration reactions and an intramolecular hydrosilylation/Fleming- Tamao oxidation sequence to establish seven of the hydroxy-bearing stereocenters of 34. Especially noteworthy is the fragment-assembly double allyboration reaction of 2 and 7 using reagent 3, which provides the advanced intermediate 6 with >20:1 diastereoselectivity.

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