503559-84-0 Usage
Uses
Used in Pharmaceutical Industry:
4-[4-Fluoro-2-(phenylmethoxy)phenyl]-α-methyl-2,6-bis(1-methylethyl)-5-(1-propen-1-yl)-3-Pyridinemethanol is used as a potential active pharmaceutical ingredient for the development of new drugs. Its unique structure and functional groups may offer novel therapeutic properties and mechanisms of action, contributing to the advancement of medicine.
Used in Agrochemical Industry:
In the agrochemical industry, 4-[4-Fluoro-2-(phenylmethoxy)phenyl]-α-methyl-2,6-bis(1-methylethyl)-5-(1-propen-1-yl)-3-Pyridinemethanol is used as a potential candidate for the development of new pesticides or herbicides. Its specific chemical properties may provide effective control of pests and weeds, enhancing crop protection and yield.
Used in Laboratory Research:
4-[4-Fluoro-2-(phenylmethoxy)phenyl]-α-methyl-2,6-bis(1-methylethyl)-5-(1-propen-1-yl)-3-Pyridinemethanol is used as a research compound in various scientific studies. Its synthesis, properties, and potential applications are of interest to chemists and researchers, who aim to explore its capabilities and optimize its use in different fields.
Used in Chemical Synthesis:
4-[4-Fluoro-2-(phenylmethoxy)phenyl]-α-methyl-2,6-bis(1-methylethyl)-5-(1-propen-1-yl)-3-Pyridinemethanol serves as a key intermediate in the synthesis of other complex organic molecules. Its unique structure and functional groups make it a valuable building block for the creation of new compounds with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 503559-84-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,5,5 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 503559-84:
(8*5)+(7*0)+(6*3)+(5*5)+(4*5)+(3*9)+(2*8)+(1*4)=150
150 % 10 = 0
So 503559-84-0 is a valid CAS Registry Number.
503559-84-0Relevant academic research and scientific papers
Integration of optimized substituent patterns to produce highly potent 4-aryl-pyridine glucagon receptor antagonists
Ladouceur, Gaetan H.,Cook, James H.,Hertzog, Donald L.,Jones,Hundertmark, Thomas,Korpusik, Mary,Lease, Timothy G.,Livingston, James N.,MacDougall, Margit L.,Osterhout, Martin H.,Phelan, Kathleen,Romero, Romulo H.,Schoen, William R.,Shao, Chunning,Smith, Roger A.
, p. 3421 - 3424 (2007/10/03)
Optimized substituent patterns in 4-aryl-pyridine glucagon receptor antagonists were merged to produce highly potent derivatives containing both a 3-[(1R)-hydroxyethyl] and a 2′-hydroxy group. Due to restricted rotation of the phenyl-pyridine bond, these analogues exist as four isomers. A diastereoselective methylcopper reaction was developed to facilitate the synthesis, and single isomers were isolated with activities in the range IC50=10-25 nM.
