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(2R,3R)-2-phenyl-1-<1,2-2H2>ethanol is a chiral, deuterated organic compound with a molecular formula of C8D2H8O. It features a 2-phenylethyl structure, where the phenyl group is attached to a chiral center at the 2-position, and the 1-position is occupied by a deuterated hydroxyl group. The compound has two chiral centers, with the R-configuration at both the 2 and 3 positions, indicating that the hydroxyl group and the phenyl group are on the same side of the molecule when viewed from the 1-position. This specific stereochemistry is important in various chemical and pharmaceutical applications, as the spatial arrangement of atoms can significantly influence the compound's properties and interactions with other molecules.

78684-43-2

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78684-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78684-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,8 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78684-43:
(7*7)+(6*8)+(5*6)+(4*8)+(3*4)+(2*4)+(1*3)=182
182 % 10 = 2
So 78684-43-2 is a valid CAS Registry Number.

78684-43-2Relevant academic research and scientific papers

Synthesis of (2R,3R)- and (2S,3S)-Oxirane and Application of It to the Synthesis of Chirally Labeled Homoserine

Schwab, John M.,Tapan, Ray,Ho, Chorng-Kei

, p. 1057 - 1063 (2007/10/02)

(2R,3R)- and (2S,3S)-oxirane have been synthesized from 2-propynol, the key step being the asymmetric epoxidation of (E)-3-(triphenylsilyl)-2-propenol.To determine the enantiomeric purities of the oxiranes, they were reacted with phenyllithium,

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