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(1R,2S)-1-acetoxymethyl-2-hydroxymethylcyclopropane is a chiral organic compound characterized by its unique cyclopropane ring structure, which consists of three carbon atoms bonded in a cyclic manner. The compound features a 1R,2S configuration, indicating that the hydroxyl group is on the right side (R) and the acetoxymethyl group is on the left side (S) when viewed from the perspective of the cyclopropane ring. The acetoxymethyl group is an ester derived from acetic acid, while the hydroxymethyl group contains an alcohol functional group. (1R,2S)-1-acetoxymethyl-2-hydroxymethylcyclopropane is of interest in organic chemistry due to its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its role as a building block for more complex molecules. Its chirality and cyclic structure make it a valuable target for studies in asymmetric synthesis and the development of new methodologies for the preparation of enantiomerically pure compounds.

98516-04-2

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98516-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98516-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,5,1 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 98516-04:
(7*9)+(6*8)+(5*5)+(4*1)+(3*6)+(2*0)+(1*4)=162
162 % 10 = 2
So 98516-04-2 is a valid CAS Registry Number.

98516-04-2Relevant academic research and scientific papers

ENZYMATIC HYDROLYSIS OF CYCLOPROPANES. TOTAL SYNTHESIS OF OPTICALLY PURE DICTYOPTERENES A AND C'.

Grandjean, D.,Pale, P.,Chuche, J.

, p. 1215 - 1230 (2007/10/02)

Enzymatic hydrolysis of cis-1,2-bis(butyryloxymethyl)cyclopropane 3 under optimized conditions gives, in quantitative yield, optically pure cis-(1S,2R)-1-hydroxymethyl-2-butyryloxymethylcyclopropane 1.This compound is a versatile cyclopropane synthon as exemplified by the total synthesis of optically pure seaweed pheromones Dictyopterenes A and C'.

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