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The chemical compound "5-Oxaspiro[2.4]heptane-1-carboxylic acid, 6-(2R)-1,4-dioxaspiro[4.5]dec-2-yl-4-methoxy-7-(phenylmethoxy)-, ethyl ester, (4R,6S,7R)-" is a complex organic molecule with a unique structure. It features a spiro[2.4]heptane core, which is a seven-membered ring with a spiro connection to a five-membered oxaspiro ring. The molecule also contains a 1,4-dioxaspiro[4.5]decane moiety, which adds to its complexity. The presence of a 4-methoxy group and a 7-phenylmethoxy group further modifies the molecule's properties. The ethyl ester functional group indicates that it is an ester derivative of the parent carboxylic acid. The stereochemistry of the molecule is specified by the (4R,6S,7R) notation, which describes the arrangement of atoms in three-dimensional space. 5-Oxaspiro[2.4]heptane-1-carboxylic acid, 6-(2R)-1,4-dioxaspiro[4.5]dec-2-yl-4-methoxy-7-(phenylmethoxy)-, ethyl ester, (4R,6S,7R)- is likely to have specific applications in pharmaceuticals or as a synthetic intermediate due to its intricate structure and functional groups.

569656-69-5

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569656-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 569656-69-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,9,6,5 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 569656-69:
(8*5)+(7*6)+(6*9)+(5*6)+(4*5)+(3*6)+(2*6)+(1*9)=225
225 % 10 = 5
So 569656-69-5 is a valid CAS Registry Number.

569656-69-5Relevant academic research and scientific papers

Synthesis of spirocycles via ring closing metathesis of heterocycles carrying gem-diallyl substituents obtained via ring opening of (halomethyl)cyclopropanes with allyltributyltin

Gurjar, Mukund K.,Ravindranadh, Somu V.,Sankar, Kuppusamy,Karmakar, Sukhen,Cherian, Joseph,Chorghade, Mukund S.

, p. 1366 - 1373 (2007/10/03)

In the presence of allyl tri-n-butyltin-AlBN, cyclopropylmethyl bromides/xanthates undergo ring-opening reaction with concomitant formation of geminal diallyl derivatives in good yields. The ring closing metathesis reactions on geminal diallyl derivatives with Grubbs' catalyst provided spirocyclopentenyl products. Combination of these two methodologies has been applied to the synthesis of mono-, bis-cyclopentyl-carbohydrates as well as spirocyclopentylproline derivatives.

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