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(3R,5S)-3-Isopropyl-3-methyl-5-phenyl-[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 isopropyl group at the 3-position, a methyl group at the 3-position, and a phenyl group at the 5-position. The compound exhibits two chiral centers, with the R-configuration at the 3-position and the S-configuration at the 5-position. This specific arrangement of substituents and chiral centers contributes to its distinct chemical and physical properties, making it a potentially valuable compound in various applications, such as pharmaceuticals or materials science, where stereochemistry plays a crucial role.

86766-16-7

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86766-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86766-16-7 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 86766-16:
(7*8)+(6*6)+(5*7)+(4*6)+(3*6)+(2*1)+(1*6)=177
177 % 10 = 7
So 86766-16-7 is a valid CAS Registry Number.

86766-16-7Downstream Products

86766-16-7Relevant academic research and scientific papers

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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