848949-85-9 Usage
Uses
Used in Biochemistry Research:
L-Leucine, 4-fluoro-, ethyl ester, sulfate (1:1) is used as a research compound for studying the interactions and effects of its components on biological systems. The presence of the fluoro group and ethyl ester may provide insights into the compound's reactivity and potential applications in various biochemical processes.
Used in Molecular Biology Research:
Used in Medicinal Chemistry:
Used in Drug Delivery Systems:
Check Digit Verification of cas no
The CAS Registry Mumber 848949-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,9,4 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 848949-85:
(8*8)+(7*4)+(6*8)+(5*9)+(4*4)+(3*9)+(2*8)+(1*5)=249
249 % 10 = 9
So 848949-85-9 is a valid CAS Registry Number.
848949-85-9Relevant academic research and scientific papers
PROCESS FOR PREPARING FLUOROLEUCINE ALKYL ESTERS
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, (2013/10/21)
This invention relates to a resolution process for the preparation of fluoroleucine alkyl esters.
An efficient chemoenzymatic approach to (S)-γ-fluoroleucine ethyl ester
Limanto, John,Shafiee, Ali,Devine, Paul N.,Upadhyay, Veena,Desmond, Richard A.,Foster, Bruce R.,Gauthier Jr., Donald R.,Reamer, Robert A.,Volante
, p. 2372 - 2375 (2007/10/03)
(Chemical Equation Presented) An asymmetric synthesis of (S)-γ-fluoroleucine ethyl ester 1 is described. The key transformation involves a lipase-catalyzed dynamic ring-opening of 2-(3-butenyl)azlactone 7b with EtOH to give amide ester (S)-6b in 84% enant
Process for preparing fluoroleucine alkyl esters
-
, (2010/02/14)
This invention relates to a stereoselective preparation of fluoroleucine alkyl esters.
