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1,3-Dioxaspiro[4.5]dec-7-en-4-ol, 2-(1,1-dimethylethyl)-8-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-6-[( 1E)-3-hydroxy-2-methyl-1-propenyl]-9-methyl-, (2R,5S,6R,9R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

497065-29-9

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497065-29-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 497065-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,7,0,6 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 497065-29:
(8*4)+(7*9)+(6*7)+(5*0)+(4*6)+(3*5)+(2*2)+(1*9)=189
189 % 10 = 9
So 497065-29-9 is a valid CAS Registry Number.

497065-29-9Downstream Products

497065-29-9Relevant academic research and scientific papers

Studies on the synthesis of kijanolide: Synthesis of an advanced seco-acid intermediate

Roush, William R.,Chen, Hou,Reilly, Melissa L.

, p. 259 - 282 (2007/10/03)

A synthesis of an advanced seco acid intermediate (7) in a projected total synthesis of kijanolide is described. Key steps in the synthesis of 7 include the highly diastereoselective allylation reaction of 15, the Suzuki cross coupling of dienyl iodide (11) and vinylboronic acid (12), and the IMDA reaction of 9. Elaboration of the spirotetronic acid unit of 7 was accomplished by a Dieckmann cyclization of the α-acetoxy ester intermediate derived from the IMDA cycloadduct (39).

A Highly Diastereo- and Enantioselective Synthesis of the Top Half of Kijanolide

Roush, William R.,Brown, Bradley B.

, p. 2151 - 2161 (2007/10/02)

A highly diastereo- and enantioselective synthesis of spirotetronate 4 corresponding to the top half of kijanolide is reported.This synthesis features the novel exo-selective Diels-Alder reaction of triene 6 and the chiral, nonracemic dienophiles (R)-7 an

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