3528-56-1 Usage
General Description
1-(2-FURYLMETHYL)-1H-PYRAZOL-5-AMINE, also known as FP-AM, is a chemical compound with the molecular formula C9H9N3O. It is a heterocyclic amine with a pyrazole ring and a furan moiety attached to the nitrogen atom. FP-AM has been studied for its potential therapeutic properties, including its activity as a kinase inhibitor. It has also been investigated for its potential use in the development of new medications for various diseases. The compound may have applications in the field of medicinal chemistry and drug discovery due to its unique structure and potential biological activity. However, further research is needed to fully understand its pharmacological properties and potential use in clinical settings.
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 articles and documents
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.
