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(E,E,7S)-8-<(2R,6S)-6-<(2S,3R,4S,6R,7R,8R,9S,10S,11S)-2-methoxy-3,7,9,11-tetramethyl-8,10-dihydroxy-4,6-((R)-para-methoxybenzylidenedioxy)-13-((2S,4R,6S)-2-methyl-4-methoxytetrahydropyran-6-yl)-tridecan-1-yl>-5,6-dihydro-2H-pyran-2-yl>-7-tert-butyldi... is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

158751-35-0

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158751-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 158751-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,7,5 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 158751-35:
(8*1)+(7*5)+(6*8)+(5*7)+(4*5)+(3*1)+(2*3)+(1*5)=160
160 % 10 = 0
So 158751-35-0 is a valid CAS Registry Number.

158751-35-0Relevant academic research and scientific papers

The total synthesis of swinholide A. Part 4: Synthesis of swinholide A and isoswinholide A from the protected monomeric seco acid, pre-swinholide A

Paterson, Ian,Yeung, Kap-Sun,Ward, Richard A.,Smith, Julian D.,Cuimming, John G.,Lamboley, Serge

, p. 9467 - 9486 (1995)

Swinholide A and isoswinholide A were synthesized in 7 steps from the fully protected seco acid 4. Key steps include: (i) bimolecular acylation, 7 + 10 → 12, (ii) selective hydrolysis of the methyl ester, 16 → 17, and (iii) regioselective macrolactonisati

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