3528-56-1 Usage
Uses
Used in Medicinal Chemistry:
1-(2-FURYLMETHYL)-1H-PYRAZOL-5-AMINE is used as a chemical compound in medicinal chemistry for its potential therapeutic properties. Its unique structure and biological activity make it a candidate for the development of new medications for various diseases.
Used in Drug Discovery:
In the field of drug discovery, 1-(2-FURYLMETHYL)-1H-PYRAZOL-5-AMINE is utilized as a starting point for the design and synthesis of novel therapeutic agents. Its potential as a kinase inhibitor highlights its role in identifying and developing new drugs that can target specific biological pathways.
Used in Kinase Inhibition Research:
1-(2-FURYLMETHYL)-1H-PYRAZOL-5-AMINE is used as a kinase inhibitor in research settings to study its effects on various cellular processes. Understanding its interaction with kinases can lead to the development of targeted therapies for diseases where kinase activity is implicated.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1-(2-FURYLMETHYL)-1H-PYRAZOL-5-AMINE is employed as a key component in the formulation of new drugs. Its potential applications in treating various diseases make it a valuable asset in the creation of innovative medicinal products.
Check Digit Verification of cas no
The CAS Registry Mumber 3528-56-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3528-56:
(6*3)+(5*5)+(4*2)+(3*8)+(2*5)+(1*6)=91
91 % 10 = 1
So 3528-56-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N3O/c9-8-3-4-10-11(8)6-7-2-1-5-12-7/h1-5H,6,9H2
3528-56-1Relevant academic research and scientific papers
Approach to the library of fused pyridine-4-carboxylic acids by combes-type reaction of acyl pyruvates and electron-rich amino heterocycles
Volochnyuk, Dmitriy M.,Ryabukhin, Sergey V.,Plaskon, Andrey S.,Dmytriv, Yuri V.,Grygorenko, Oleksandr O.,Mykhailiuk, Pavel K.,Krotko, Dmitriy G.,Pushechnikov, Alexei,Tolmachev, Andrey A.
scheme or table, p. 510 - 517 (2010/09/05)
A library of fused pyridine-4-carboxylic acids (including pyrazolo[3,4-b]pyridines, isoxazolo[5,4-b]pyridines, furo[2,3-b]pyridines, thieno[2,3-b]pyridines, and pyrido[2,3-d]pyrimidines) was generated by Combes-type reaction of acyl pyruvates and electron-rich amino heterocycles followed by hydrolysis of the ester. The library members were also demonstrated to undergo the standard combinatorial transformations including amide coupling and esterification, as well as less common heterocyclizations to 1,2,4-triazoles and 1,2,4-oxadiazoles.
