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86766-10-1

(3R,5R)-3-Ethyl-3,5-diphenyl-[1,2]dioxolane is a chiral organic compound characterized by its unique structure and properties. It features a [1,2]dioxolane ring, which is a five-membered ring containing two oxygen atoms, and is further substituted with an ethyl group at the 3-position and two phenyl groups at the 5-position. The compound exhibits a specific stereochemistry, with the R configuration at both the 3 and 5 positions, indicating that the substituents at these positions are arranged in a specific three-dimensional orientation. This chirality is significant as it can influence the compound's reactivity and biological activity. The compound is of interest in organic chemistry and may have applications in the synthesis of pharmaceuticals and other specialty chemicals due to its unique structural features and potential for asymmetric synthesis.

86766-10-1

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86766-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86766-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,6 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86766-10:
(7*8)+(6*6)+(5*7)+(4*6)+(3*6)+(2*1)+(1*0)=171
171 % 10 = 1
So 86766-10-1 is a valid CAS Registry Number.

86766-10-1Relevant articles and documents

SYNTHESIS AND DECOMPOSITION OF E- AND Z-3,3,5-TRISUBSTITUTED 1,2-DIOXOLANES.

Yoshida,Miura,Nojima,Kusabayashi

, p. 6279 - 6285 (2007/10/02)

The reactions of a number of ozonides and olefins in the presence of boron trifluoride-diethyl ether gave the corresponding mixtures of (E)- and (Z)-1,2-dioxolanes in 12-70% yield. The decomposition of the E-Z isomeric 1,2-dioxolanes 3a-c was undertaken under a variety of conditions, i. e. , thermal, TiCl//4-mediated, FeSO//4-catalyzed, and LiAlH//4-mediated decompositions.

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