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[(2-{6-(tert-butyl-dimethyl-silanyloxy)-3-[2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-4-methylene-cyclohex-2-enyl}-ethyl)-dimethyl-silanyl]-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

828915-80-6

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  • [(2-{6-(tert-butyl-dimethyl-silanyloxy)-3-[2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-4-methylene-cyclohex-2-enyl}-ethyl)-dimethyl-silanyl]-benzene

    Cas No: 828915-80-6

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  • [(2-{6-(tert-butyl-dimethyl-silanyloxy)-3-[2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-ethyl]-4-methylene-cyclohex-2-enyl}-ethyl)-dimethyl-silanyl]-benzene

    Cas No: 828915-80-6

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828915-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 828915-80-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,8,9,1 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 828915-80:
(8*8)+(7*2)+(6*8)+(5*9)+(4*1)+(3*5)+(2*8)+(1*0)=206
206 % 10 = 6
So 828915-80-6 is a valid CAS Registry Number.

828915-80-6Relevant articles and documents

A concise sultone route to highly oxygenated 1,10-seco-eudesmanolides - enantioselective total synthesis of the antileukemic sesquiterpene lactones (-)-eriolanin and (-)-eriolangin

Merten, Joern,Hennig, Andre,Schwab, Pia,Froehlich, Roland,Tokalov, Sergey V.,Gutzeit, Herwig O.,Metz, Peter

, p. 1144 - 1161 (2007/10/03)

Using a sultone as the key intermediate, the first enantioselective total synthesis of the antileukemic 1,10-seco-eudesmanolides (-)-eriolanin (1) and (-)-eriolangin (2) was achieved, which also established the hitherto unknown absolute configuration of t

Enantioselective total synthesis of the highly oxygenated 1,10-seco-eudesmanolides eriolanin and eriolangin

Merten, Joern,Froehlich, Roland,Metz, Peter

, p. 5991 - 5994 (2007/10/03)

Sultones of swing: A sultone served as the key intermediate in the first enantioselective total syntheses of the bioactive title compounds (see scheme), the absolute configuration of which is now established. Starting from 2-bromo-1-(2-furyl)ethanone, 24

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