60406-64-6 Usage
Biological and Pharmaceutical Applications
It has potential uses in the medical field due to its unique properties.
Hypoxia-inducible Factor Prolyl Hydroxylase Inhibitor
It inhibits the activity of prolyl hydroxylase, a key enzyme involved in the regulation of the body's response to low oxygen levels.
Stimulation of Erythropoietin Production
By inhibiting prolyl hydroxylase, it leads to increased production of erythropoietin, a hormone that stimulates red blood cell production.
Treatment of Anemia
It has shown promise in treating anemia, a condition characterized by a lack of red blood cells or hemoglobin.
Potential Treatment for Chronic Kidney Disease
It has been studied for its potential to treat chronic kidney disease, a condition that affects the kidneys' ability to filter waste from the blood.
Treatment of Hypoxia-related Conditions
It has been investigated for its potential use in treating conditions related to low oxygen levels, such as ischemic diseases and cancer.
Molecular Structure
The compound consists of a 1,2,4-triazole ring with a phenyl group at the 3-position and a trifluoromethyl group at the 5-position.
Check Digit Verification of cas no
The CAS Registry Mumber 60406-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,0 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60406-64:
(7*6)+(6*0)+(5*4)+(4*0)+(3*6)+(2*6)+(1*4)=96
96 % 10 = 6
So 60406-64-6 is a valid CAS Registry Number.
60406-64-6Relevant articles and documents
Five-to-six membered ring-rearrangements in the reaction of 5-perfluoroalkyl-1,2,4-oxadiazoles with hydrazine and methylhydrazine
Buscemi, Silvestre,Pace, Andrea,Piccionello, Antonio Palumbo,Pibiri, Ivana,Vivona, Nicolo,Giorgi, Gianluca,Mazzanti, Andrea,Spinelli, Domenico
, p. 8106 - 8113 (2007/10/03)
The hydrazinolysis reaction of 5-perfluoroalkyl-1,2,4-oxadiazoles with hydrazine or methylhydrazine as bidentate nucleophiles has been investigated. The reaction occurred through the addition of the bidentate nucleophile to the C(5)-N(4) double bond of th
