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(E)-4-[(1R,5S,7R)-1-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-6-(2,2,2-trifluoro-acetyl)-6-aza-spiro[4.5]dec-7-yl]-2-methyl-but-2-enoic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

403507-08-4

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  • (E)-4-[(1R,5S,7R)-1-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-6-(2,2,2-trifluoro-acetyl)-6-aza-spiro[4.5]dec-7-yl]-2-methyl-but-2-enoic acid ethyl ester

    Cas No: 403507-08-4

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  • Shandong Xingshun New Material Co., Ltd.
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  • (E)-4-[(1R,5S,7R)-1-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-1-methyl-ethyl]-6-(2,2,2-trifluoro-acetyl)-6-aza-spiro[4.5]dec-7-yl]-2-methyl-but-2-enoic acid ethyl ester

    Cas No: 403507-08-4

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  • Shanghai Scochem Technology Co., Ltd.
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403507-08-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 403507-08-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,5,0 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 403507-08:
(8*4)+(7*0)+(6*3)+(5*5)+(4*0)+(3*7)+(2*0)+(1*8)=104
104 % 10 = 4
So 403507-08-4 is a valid CAS Registry Number.

403507-08-4Downstream Products

403507-08-4Relevant articles and documents

Formal syntheses of (±)-pinnaic acid and (±)-halichlorine

Andrade, Rodrigo B.,Martin, Stephen F.

, p. 5733 - 5735 (2007/10/03)

(Chemical Equation Presented) Concise formal syntheses of marine alkaloids (±)-pinnaic acid (1) and (±)-halichlorine (2) have been accomplished from a common intermediate. The syntheses illustrate the utility of selective olefin cross metathesis methodolo

Concise stereoselective routes to advanced intermediates related to natural and unnatural pinnaic acid

Carson,Kim,Hentemann,Trauner,Danishefsky

, p. 4450 - 4452 (2007/10/03)

Important intermediates: In an effort to synthesize and determine the stereo-chemistry of pinnaic acid, C14-epimeric aldehydes 1 and 2 were generated from Meyers' lactam 3. A key step in the parallel syntheses is a highly stereoselective vinylogous Michae

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