666743-31-3 Usage
Uses
Used in Organic Synthesis:
Ethanone, 1-[2-(phenylseleno)phenyl]is utilized as a reagent in organic synthesis for the preparation of a variety of organic compounds. The presence of the phenylseleno group imparts specific reactivity and selectivity to the molecule, facilitating targeted reactions and enhancing the efficiency of the synthesis process.
Used in Pharmaceutical Development:
Ethanone, 1-[2-(phenylseleno)phenyl]is employed in the development of novel pharmaceuticals due to its versatile chemical properties. Its ability to modify molecular structures allows for the creation of new drug candidates with potentially improved therapeutic effects and reduced side effects.
Used in Material Science:
Ethanone, 1-[2-(phenylseleno)phenyl]also holds potential in material science, where its unique chemical characteristics can be leveraged to develop new materials with specific properties for various applications, such as in electronics, coatings, or advanced materials for industrial use.
Check Digit Verification of cas no
The CAS Registry Mumber 666743-31-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,6,7,4 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 666743-31:
(8*6)+(7*6)+(6*6)+(5*7)+(4*4)+(3*3)+(2*3)+(1*1)=193
193 % 10 = 3
So 666743-31-3 is a valid CAS Registry Number.
666743-31-3Relevant academic research and scientific papers
Preparation of chiral organochalcogeno-α-methylbenzyl alcohols via biocatalysis. The role of Daucus carota root
Comasseto, Jo?o V.,Omori, álvaro T.,Porto, André L. M.,Andrade, Leandro H.
, p. 473 - 476 (2007/10/03)
A series of organochalcogeno acetophenones 3 has been submitted to the action of enzymes from Daucus carota root. Some of the chalcogeno ketones tested afforded the chiral organochalcogeno-α-methylbenzyl alcohols 4 in excellent enantiomeric excesses (>99%), under mild and environmentally friendly conditions. The stereoselectivity of the reduction is in accordance with Prelog's rule. Enzymatic kinetic resolution as alternative process was used to obtain the chiral ortho-organochalcogeno-α-methylbenzyl alcohols in excellent enantiomeric excess (>99%).
