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5-{(3aS,5R,6R,6aS)-5-(tert-Butyl-dimethyl-silanyloxy)-6-[(E)-(R)-3-(tert-butyl-dimethyl-silanyloxy)-4-m-tolyl-but-1-enyl]-1,3a,4,5,6,6a-hexahydro-pentalen-2-yl}-pentanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

906000-89-3

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906000-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 906000-89-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,0,0 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 906000-89:
(8*9)+(7*0)+(6*6)+(5*0)+(4*0)+(3*0)+(2*8)+(1*9)=133
133 % 10 = 3
So 906000-89-3 is a valid CAS Registry Number.

906000-89-3Downstream Products

906000-89-3Relevant academic research and scientific papers

Cross metathesis as a general strategy for the synthesis of prostacyclin and prostaglandin analogues

Sheddan, Neil A.,Mulzer, Johann

, p. 3101 - 3104 (2007/10/03)

A cross metathesis (CM) approach has been successfully applied to introduce fully functionalized ω-side chain appendages of various prostacyclin and prostaglandin analogues, resulting in high (E)-selectivities for the C13-C14 double bond and leading to the total syntheses of isocarbacyclin, 15R-TIC, carbacyclin, and PGF2α, and the formal syntheses of 15-deoxy-TIC and PGJ2.

Exploration of ω-side chain addition strategies for the syntheses of isocarbacyclin and 15R-16-(m-tolyl)-17,18,19,20-tetranorisocarbacyclin

Sheddan, Neil A.,Mulzer, Johann

, p. 4127 - 4130 (2008/09/19)

We describe alternative access to prostacyclin analogues by means of two ω-side chain addition strategies: Grignard reagent addition to an α,β-unsaturated Weinreb amide, followed by diastereoselective reduction of the corresponding enone system, and imple

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