CAS 1998-63-6
:6-chloro-2-(trifluoromethyl)-5H-purine
Description:
6-Chloro-2-(trifluoromethyl)-5H-purine is a purine derivative characterized by the presence of a chlorine atom at the 6-position and a trifluoromethyl group at the 2-position of the purine ring. This compound exhibits a fused bicyclic structure typical of purines, which are essential components of nucleic acids. The trifluoromethyl group contributes to its lipophilicity and can influence its biological activity, making it of interest in medicinal chemistry. The chlorine substituent can also affect the compound's reactivity and interaction with biological targets. This substance is typically used in research settings, particularly in studies related to nucleic acid chemistry and potential pharmaceutical applications. Its unique structural features may impart specific properties such as solubility, stability, and reactivity, which are crucial for its function in biological systems or as a synthetic intermediate. As with many halogenated compounds, safety precautions should be observed due to potential toxicity and environmental impact.
Formula:C6H2ClF3N4
InChI:InChI=1/C6H2ClF3N4/c7-3-2-4(12-1-11-2)14-5(13-3)6(8,9)10/h1-2H
SMILES:C1=NC2C(=NC(=NC2=N1)C(F)(F)F)Cl
Synonyms:- 6-Chloro-2-trifluoromethyl-7H-purine
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
6-Chloro-2-(trifluoromethyl)-9H-purine
CAS:Formula:C6H2ClF3N4Purity:97%Color and Shape:SolidMolecular weight:222.55516-Chloro-2-(trifluoromethyl)-9H-purine
CAS:6-Chloro-2-(trifluoromethyl)-9H-purinePurity:97%Molecular weight:222.56g/mol6-Chloro-2-(trifluoromethyl)-9H-purine
CAS:Heterocyclic Compounds - Purines; Intermediates and Building Blocks - Nucleoside bases; Multi-functional; Scaffolds and TemplatesFormula:C6H2ClF3N4Color and Shape:SolidMolecular weight:222.56



