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(R*,S*)-α-Ethyl-2-methyloxiranemethanol is a chiral organic compound characterized by its unique structure, which includes an oxirane (epoxy) ring, an ethyl group, and a methyl group. (R*,S*)-α-Ethyl-2-methyloxiranemethanol is a specific stereoisomer, with the R* and S* designations indicating the configuration of the molecule's chiral centers. It is synthesized through a series of chemical reactions and is used in various applications, such as in the production of pharmaceuticals and other specialty chemicals. Due to its chiral nature, it is essential to control the stereochemistry during synthesis to obtain the desired isomer with specific biological activity or reactivity. The compound's properties, such as solubility and reactivity, can be influenced by its stereochemistry, making it a valuable molecule in the field of asymmetric synthesis and chiral chemistry.

84599-41-7

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84599-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84599-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,9 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84599-41:
(7*8)+(6*4)+(5*5)+(4*9)+(3*9)+(2*4)+(1*1)=177
177 % 10 = 7
So 84599-41-7 is a valid CAS Registry Number.

84599-41-7Upstream product

84599-41-7Relevant academic research and scientific papers

Stereospecific Telluride-Mediated Conversion of Glycidols to Allyl Alcohols: An Extension of the Sharpless Kinetic Resolution

Discordia, Robert P.,Dittmer, Donald C.

, p. 1414 - 1415 (1990)

Treatment of methanesulfonate esters of terminal glycidols obtained by epoxidation in the Sharpless kinetic resolution (SKR) of 1-substituted 2-propenols (secondary allyl alcohols) with telluride ion (Te2-) converts the glycidols to allyl alcohols of the same stereochemical configuration as the unreacted enantiomer from the SKR.

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