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CAS 101155-02-6

:

9-(2-fluorobenzyl)-6-(methylamino)-9H-purine

Description:
9-(2-Fluorobenzyl)-6-(methylamino)-9H-purine, with the CAS number 101155-02-6, is a purine derivative characterized by its unique structural features, including a fluorobenzyl group and a methylamino substituent. This compound belongs to a class of molecules that can exhibit biological activity, often related to their interactions with purine receptors or enzymes. The presence of the fluorobenzyl group may enhance lipophilicity and influence the compound's pharmacokinetic properties, potentially affecting its absorption, distribution, metabolism, and excretion. The methylamino group can also play a crucial role in modulating the compound's reactivity and biological interactions. As a purine analog, it may be of interest in medicinal chemistry, particularly in the development of therapeutics targeting nucleic acid processes or cellular signaling pathways. Its specific characteristics, such as solubility, stability, and reactivity, would depend on the surrounding conditions and the presence of other functional groups in the molecular structure. Further studies would be necessary to elucidate its full biological profile and potential applications.
Formula:C13H13ClFN5
InChI:InChI=1/C13H12FN5.ClH/c1-15-12-11-13(17-7-16-12)19(8-18-11)6-9-4-2-3-5-10(9)14;/h2-5,7-8H,6H2,1H3,(H,15,16,17);1H
SMILES:CNc1c2c(ncn1)n(Cc1ccccc1F)cn2.Cl
Synonyms:
  • Bw-A 78U
  • 9-((2-Fluorophenyl)methyl)-N-methyl-9H-purin-6-amine
  • Brn 4517870
  • Bw A78U
  • 9H-Purin-6-amine, 9-((2-fluorophenyl)methyl)-N-methyl-
  • 9-(2-fluorobenzyl)-N-methyl-9H-purin-6-amine
  • 9-(2-fluorobenzyl)-N-methyl-9H-purin-6-amine hydrochloride
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