31354-48-0 Usage
General Description
2-(Acetylamino)-3-pyridinol is a chemical compound with the molecular formula C8H8N2O2. It is also known by the trade name Niaprazine. 2-(Acetylamino)-3-pyridinol is used as an antiparasitic agent and as a treatment for various diseases caused by parasitic infections. It works by interfering with the formation of DNA and RNA in the parasites' cells, ultimately leading to their death. It is mainly used in veterinary medicine for the treatment of parasites in animals, but it has also shown potential in the treatment of certain human diseases. Additionally, it has been studied for its potential use as a fungicide and herbicide.
Check Digit Verification of cas no
The CAS Registry Mumber 31354-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,3,5 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 31354-48:
(7*3)+(6*1)+(5*3)+(4*5)+(3*4)+(2*4)+(1*8)=90
90 % 10 = 0
So 31354-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2/c1-5(10)9-7-6(11)3-2-4-8-7/h2-4,11H,1H3,(H,8,9,10)
31354-48-0Relevant articles and documents
NMR studies of new heterocycles tethered to purine moieties with anticancer activity
Fernández-Sáez, Nerea,Campos, Joaquín M.,Camacho, María Encarnación,Carrión, María Dora
, p. 331 - 341 (2019)
-
Synthesis of substituted 3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine as new scaffolds for potential bioactive compounds
Henry,Sánchez,Sabatié,Bénéteau,Guillaumet,Pujol
, p. 2405 - 2412 (2007/10/03)
The title compounds having different substituents on the heterocyclic framework were prepared by several methods from 2-acetamido-3-hydroxypyridine. The condensation of 2-protected-amino-3-hydroxypyridine with 2-chloroacrylonitrile or ethyl 2,3-dibromopro
FACILE SYNTHESIS OF SOME OXAZOLOPYRIDINES AND THEIR N-OXIDES VIA INTRAMOLECULAR CYCLIZATION
Tagawa, Yoshinobu,Goto, Yoshinobu
, p. 2921 - 2939 (2007/10/02)
A convenient synthesis of 3-methylisoxazolopyridine 2, 2-methyloxazolopyridine 4 and their N-oxides (12, 17 and 18) is reported.The configurations of the oximes used for the synthesis of the compounds described above are discussed through chemical and spectral studies.
