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(2R,5S)-7-([1,3]dithian-2-yl)-1-{(2S,6R)-6-[2-(4-methoxy-benzyloxy)-ethyl]-4-methylene-tetrahydropyran-2-yl}-5-methyl-4-methylene-heptan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

651302-82-8

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651302-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 651302-82-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,1,3,0 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 651302-82:
(8*6)+(7*5)+(6*1)+(5*3)+(4*0)+(3*2)+(2*8)+(1*2)=128
128 % 10 = 8
So 651302-82-8 is a valid CAS Registry Number.

651302-82-8Relevant academic research and scientific papers

Diastereoselectivity in asymmetric allylations: The role of vicinal chirality in the allyl nucleophile for SE2′ reactions with aldehydes

Williams, David R.,Meyer, Kevin G.,Shamim, Khalida,Patnaik, Samarjit

, p. 120 - 130 (2007/10/03)

A series of nonracemic homoallylic alcohols have been prepared by asymmetric allylation using the (R,R)-and (S,S)-1,2-diamino-1,2-diphenylethane bis-sulfonamide controller ligands for in situ formation of chiral B-allyl-1,3,2-diazaborolidines. Diastereofa

Leucascandrolide A: A Second Generation Formal Synthesis

Williams, David R.,Patnaik, Samarjit,Plummer, Scott V.

, p. 5035 - 5038 (2007/10/03)

(Equation presented) A convergent, second generation formal synthesis of (+)-Leucascandrolide A (1) has been efficiently achieved by providing a flexible, enantiocontrolled strategy toward the bioactive macrolactone component. Advancements for stereocontr

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