53344-73-3 Usage
Uses
Used in Pharmaceutical Synthesis:
2-chloro-4-(pyridin-4-yl)pyridine is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 2-chloro-4-(pyridin-4-yl)pyridine is employed as a building block for the creation of novel agrochemicals. Its incorporation into these compounds can lead to the development of more effective and targeted pest control solutions.
Used in Organic Compound Preparation:
2-chloro-4-(pyridin-4-yl)pyridine is utilized as a starting material for the preparation of various organic compounds. Its versatile structure enables the synthesis of a wide range of molecules with diverse properties and applications.
Used in Material Development:
2-chloro-4-(pyridin-4-yl)pyridine may have potential uses in the development of new materials. Its unique chemical properties could contribute to the creation of innovative materials with specific characteristics for various applications.
Used in Medicinal Chemistry and Drug Discovery:
Due to its potential biological activity, 2-chloro-4-(pyridin-4-yl)pyridine is of interest for further investigation in the fields of medicinal chemistry and drug discovery. Researchers may explore its interactions with biological targets and evaluate its potential as a therapeutic agent or a lead compound for the development of new drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 53344-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,4 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53344-73:
(7*5)+(6*3)+(5*3)+(4*4)+(3*4)+(2*7)+(1*3)=113
113 % 10 = 3
So 53344-73-3 is a valid CAS Registry Number.
53344-73-3Relevant academic research and scientific papers
Organocatalytic diboration involving "reductive addition" of a boron-boron-bond to 4,4′-bipyridine
Ohmura, Toshimichi,Morimasa, Yohei,Suginome, Michinori
, p. 2852 - 2855 (2015/05/20)
A 4,4′-bipyridine-based catalyst system for diboration of pyrazine derivatives was established. The catalyst cycle consists of the following two steps: (1) reductive addition of the boron-boron bond of bis(pinacolato)diboron to 4,4′-bipyridine to form N,N
Design and synthesis of 3,7-diarylimidazopyridines as inhibitors of the VEGF-receptor KDR
Wu, Zhicai,Fraley, Mark E.,Bilodeau, Mark T.,Kaufman, Mildred L.,Tasber, Edward S.,Balitza, Adrienne E.,Hartman, George D.,Coll, Kathleen E.,Rickert, Keith,Shipman, Jennifer,Shi, Bin,Sepp-Lorenzino, Laura,Thomas, Kenneth A.
, p. 909 - 912 (2007/10/03)
3,7-Diarylsubstituted imidazopyridines were designed and developed as a new class of KDR kinase inhibitors. A variety of imidazopyridines were synthesized and potent inhibitors of KDR kinase activity were identified with good aqueous solubility.
(Pyridinyl)-1,2,4-triazolo[4,3-a]pyridines
-
, (2008/06/13)
This disclosure describes novel substituted 1,2,4-triazolo[4,3-a]pyridines which possess anxioltic activity.
