83170-03-0 Usage
General Description
2-Amino-4-chloro-6-guanidinopyrimidine is a chemical compound with the molecular formula C5H5ClN6. It is a white crystalline powder with a molecular weight of 180.59 g/mol. 2-Amino-4-chloro-6-guanidinopyrimidine is commonly used in the pharmaceutical industry as an intermediate in the synthesis of various drugs, such as antiviral and anticancer medications. It is also used as a building block in the production of guanidine-based compounds. Additionally, 2-Amino-4-chloro-6-guanidinopyrimidine has been studied for its potential antiviral and anticancer properties. It is important to handle this chemical with caution and follow proper safety protocols due to its potential health hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 83170-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,7 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83170-03:
(7*8)+(6*3)+(5*1)+(4*7)+(3*0)+(2*0)+(1*3)=110
110 % 10 = 0
So 83170-03-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H7ClN6/c6-2-1-3(11-4(7)8)12-5(9)10-2/h1H,(H6,7,8,9,10,11,12)
83170-03-0Relevant articles and documents
Coordination Compounds of Copper(II) with Aminoguanidinopyrimidines
Zawadzki, H. J.
, p. 1293 - 1302 (2007/10/02)
Some new chelates of copper(II) with substituted guanidinopyrimidines have been obtained and characterized. On the basis of IR and VIS spectra the structure of the nearest environment of the central ion in these chelates has been determined. These ligands are bonded with metal ion via the nitrogens atoms of pyrimidine heterocyclic ring and guanidine group. Key words: complexes, synthesis, IR-spectra
Guanidinopyrimidine compounds, compositions and method of using as a diuretic
-
, (2008/06/13)
2,4-Amino, guanidinopyrimidines have diuretic activity. A representative species of these compounds is 2-guanidino-4-amino-6-chloroguanidine which is prepared by the stepwise replacement of first the 2-halo of a 2,4,6-trihalopyrimidine by guanidino and then the 4-halo by ammonia.
