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(3R,4R,5R,6R)-3,4,5,6-tetra(benzoyloxy)-1,7-octadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

256342-69-5

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256342-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 256342-69-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,3,4 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 256342-69:
(8*2)+(7*5)+(6*6)+(5*3)+(4*4)+(3*2)+(2*6)+(1*9)=145
145 % 10 = 5
So 256342-69-5 is a valid CAS Registry Number.

256342-69-5Downstream Products

256342-69-5Relevant academic research and scientific papers

Ruthenium carbene complexes with imidazol-2-ylidene ligands: Syntheses of conduritol derivatives reveals superior RCM activity

Ackermann, Lutz,El Tom, David,Fürstner, Alois

, p. 2195 - 2202 (2007/10/03)

Syntheses of conduritol A, E and F derivatives are described using galactitol, D-mannitol and D-glucitol, respectively, as the starting materials. The key steps of this approach comprise a Tebbe olefination reaction for the preparation of dienes 15, 21 and 27 followed by ring closing metathesis (RCM) for the formation of the polyhydroxylated cyclohexene rings of the targets. A comparative study shows that the latter transformation is best achieved with catalytic amounts of ruthenium carbene complex 3a bearing one PCy3 and one 2,3-dihydro-1H-imidazol-2-ylidene ligand in its coordination sphere. (C) 2000 Elsevier Science Ltd.

A straightforward synthesis of perbenzylated conduritols from alditols by ring closing olefin metathesis

Gallos, John K.,Koftis, Theocharis V.,Sarli, Vassiliki C.,Litinas, Konstantinos E.

, p. 3075 - 3077 (2007/10/03)

The synthesis of perbenzylated conduritols A, E and F has been achieved in six steps by formal conversion of galactitol, D-mannitol and D-glucitol into the respective terminal dienes, followed by ring closing olefin metathesis. The Royal Society of Chemistry 1999.

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