59524-88-8 Usage
General Description
2-Amino-4-hydroxy-6-iodopyrimidine is a chemical compound with the molecular formula C4H4IN3O. It is a pyrimidine derivative with an amino group at position 2, a hydroxy group at position 4, and an iodine atom at position 6. 2-AMINO-4-HYDROXY-6-IODOPYRIMIDINE is used in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential use as an antiviral and anticancer agent. 2-Amino-4-hydroxy-6-iodopyrimidine has demonstrated potential biological activity, making it of interest for further research and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 59524-88-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,2 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 59524-88:
(7*5)+(6*9)+(5*5)+(4*2)+(3*4)+(2*8)+(1*8)=158
158 % 10 = 8
So 59524-88-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H4IN3O/c5-2-1-3(9)8-4(6)7-2/h1H,(H3,6,7,8,9)
59524-88-8Relevant articles and documents
Sonogashira cross-coupling in the synthesis of acyclic nucleoside phosphonates: Preparation of 6-[(phosphonomethoxy)alkynyl]- and 6-[(phosphonomethoxy)alkyl]pyrimidines
Hockova, Dana,Masojidkova, Milena,Holy, Antonin
, p. 247 - 258 (2005)
Several 6-[(phosphonomethoxy)alkyl]pyrimidines and 6-[(phosphonomethoxy) alkynyl]-pyrimidines were prepared as saturated and unsaturated carba-analogues of antivirally active 2,4-diamino-6-[2-(phosphonomethoxy)ethoxy]pyrimidine. As the key step of their s
2-Amino-6-iodo-4-tosyloxypyrimidine: a versatile key intermediate for regioselective functionalization of 2-aminopyrimidines in 4- and 6-positions
Benderitter, Pascal,de Araújo Júnior, Jo?o Xavier,Schmitt, Martine,Bourguignon, Jean-Jacques
, p. 12465 - 12470 (2008/03/13)
2-Amino-6-iodo-4-tosyloxypyrimidine, easily prepared from commercially available material, is a key intermediate for the preparation of differentially substituted 2-aminopyrimidines by means of sequenced Suzuki and/or Sonogashira reactions.