149342-40-5 Usage
Uses
Used in Pharmaceutical Industry:
N-(4-chloro-β-hydroxy-phenethyl)-acetamide is used as a pharmaceutical intermediate for the production of various drugs. Its chemical structure and properties make it a valuable component in the synthesis of a wide range of medications, contributing to the development of novel therapeutic agents.
Used in Drug Synthesis:
As a key intermediate in drug synthesis, N-(4-chloro-β-hydroxy-phenethyl)-acetamide is employed to facilitate the creation of new pharmaceutical compounds. Its unique structure allows for the development of drugs with specific therapeutic properties, potentially leading to innovative treatments for various medical conditions.
Used in Research and Development:
In the field of research and development, N-(4-chloro-β-hydroxy-phenethyl)-acetamide serves as a crucial compound for exploring new drug candidates and understanding their mechanisms of action. Its application in this context aids in the advancement of pharmaceutical science and the discovery of more effective medications.
Check Digit Verification of cas no
The CAS Registry Mumber 149342-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,3,4 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 149342-40:
(8*1)+(7*4)+(6*9)+(5*3)+(4*4)+(3*2)+(2*4)+(1*0)=135
135 % 10 = 5
So 149342-40-5 is a valid CAS Registry Number.
149342-40-5Relevant academic research and scientific papers
Baker's Yeast Reduction of α-(Acylamino)acetophenones and Lipase Catalyzed Resolution of 2-Acylamino-1-arylethanols
Izumi, Taeko,Fukaya, Katsumi
, p. 1216 - 1221 (2007/10/02)
Enzymatic reduction of α-acylaminoacetophenones with fermenting baker's yeast afforded optically active (R)-2-acylamino-1-arylethanols.Furthermore, lipase-catalyzed resolution of the 2-acylamino-1-arylethanols using vinyl acetate as an acyl donor resulted in the formation of (S)-1-acetoxy-2-acylamino-1-arylethanols and (R)-2-acylamino-1-arylethanols.
