774225-86-4 Usage
Uses
Used in Pharmaceutical Industry:
Ethanone, 1-[6-(1-hydroxyethyl)-2-pyridinyl](9CI) is used as a potential pharmaceutical compound for its unique structural features. Its pyridine ring, ketone group, and hydroxyethyl group may contribute to its interaction with biological targets, offering opportunities for drug development.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Ethanone, 1-[6-(1-hydroxyethyl)-2-pyridinyl](9CI) is utilized as a structural template for designing new drugs. Its chemical properties and potential to bind with biological receptors make it a valuable starting point for creating novel therapeutic agents.
Further research and study are necessary to fully understand the compound's applicability and potential uses in the medical and pharmaceutical fields. This includes exploring its pharmacological properties, mechanism of action, and safety profile, as well as identifying specific therapeutic areas where it may be most effective.
Check Digit Verification of cas no
The CAS Registry Mumber 774225-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,4,2,2 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 774225-86:
(8*7)+(7*7)+(6*4)+(5*2)+(4*2)+(3*5)+(2*8)+(1*6)=184
184 % 10 = 4
So 774225-86-4 is a valid CAS Registry Number.
774225-86-4Relevant academic research and scientific papers
Szatzker, Gabor,Moczar, Ildiko,Kolonits, Pal,Novak, Lajos,Huszthy, Peter,Poppe, Laszlo
, p. 2483 - 2490 (2004)
Several lipases were tested for the enantiomerically selective acetylation of racemic 1-[6-(1-hydroxyethyl)-pyridin-2-yl]ethanone rac-2 to yield alcohol (S)-2 and acetate (R)-3. Acetylation of a diastereomeric mixture of racemic and meso-2,6-bis(1-hydroxy-ethyl)pyridine, rac/meso-4, with the most selective Novozym 435 lipase in vinyl acetate resulted in a mixture of enantiopure diol (S,S)-4, monoacetate (R,S)-5 and diacetate (R,R)-6. Hydrolysis of the mixture of racemic and meso-2,6-bis(1-acetoxyethyl)pyridine rac/meso-6 by the same enzyme gave the pure enantiomers of diol (R,R)-4, monoacetate (S,R)-5 and diacetate (S,S)-6. Using further chemical and enzymatic steps alcohol (R)-2, acetate (S)-3, (S,S)- and (R,R)-monoacetates (S,S)-5 and (R,R)-5, meso-4 and its acetate meso-6 were also prepared and characterized.
