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CAS 7013-21-0

:

2-chloro-9-methyl-9H-purin-6-amine

Description:
2-Chloro-9-methyl-9H-purin-6-amine, with the CAS number 7013-21-0, is a purine derivative characterized by its structural features that include a chlorine atom at the 2-position and a methyl group at the 9-position of the purine ring. This compound exhibits properties typical of purines, such as being a heterocyclic aromatic organic compound. It is likely to be soluble in polar solvents due to the presence of amino and chloro functional groups, which can engage in hydrogen bonding. The compound may exhibit biological activity, potentially acting as a nucleobase analog, which could influence nucleic acid metabolism or cellular processes. Its reactivity may be influenced by the presence of the chlorine atom, which can participate in substitution reactions. As with many purine derivatives, it may have applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting nucleic acid-related pathways. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.
Formula:C6H6ClN5
InChI:InChI=1/C6H6ClN5/c1-12-2-9-3-4(8)10-6(7)11-5(3)12/h2H,1H3,(H2,8,10,11)
SMILES:Cn1cnc2c(N)nc(Cl)nc12
Synonyms:
  • 9H-purin-6-amine, 2-chloro-9-methyl-
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