78419-62-2 Usage
Uses
Used in Organic Synthesis:
(2,3-diphenyloxiran-2-yl)methanol serves as a reactant or intermediate in organic synthesis, facilitating the creation of a wide array of pharmaceuticals and fine chemicals. Its presence in these processes is crucial due to its ability to undergo ring-opening reactions and functional group transformations, which are key steps in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2,3-diphenyloxiran-2-yl)methanol is utilized as a building block for the development of pharmaceuticals. Its unique reactivity and solubility properties make it a valuable component in the design and synthesis of new drugs, contributing to the advancement of medicinal compounds with potential therapeutic applications.
Used in Chemical Processes:
(2,3-diphenyloxiran-2-yl)methanol's solubility in polar solvents, attributed to the methanol functional group, makes (2,3-diphenyloxiran-2-yl)methanol suitable for use in various chemical processes. Its versatility in participating in different types of chemical reactions positions it as an essential component in the production of specialty chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 78419-62-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,1 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78419-62:
(7*7)+(6*8)+(5*4)+(4*1)+(3*9)+(2*6)+(1*2)=162
162 % 10 = 2
So 78419-62-2 is a valid CAS Registry Number.
78419-62-2Relevant academic research and scientific papers
Asymmetric epoxidation of allylic alcohols catalyzed by new chiral vanadium(V) complexes
Wu, Hsyueh-Liang,Uang, Biing-Jiun
, p. 2625 - 2628 (2007/10/03)
Vanadium catalysts bearing (+)-ketopinic acid-based chiral hydroxamic acids as constituent ligands are investigated in the asymmetric epoxidation of allylic alcohols. Chiral ligands lacking an N-substituent and those having a bulkier aryl group in the bor
