CAS 56025-87-7
:2,6-Dichloro-7-(phenylmethyl)-7H-purine
Description:
2,6-Dichloro-7-(phenylmethyl)-7H-purine, with the CAS number 56025-87-7, is a purine derivative characterized by its unique structure that includes two chlorine atoms at the 2 and 6 positions and a phenylmethyl group at the 7 position of the purine ring. This compound typically appears as a solid and is soluble in organic solvents, reflecting its non-polar characteristics due to the presence of the phenylmethyl group. It exhibits biological activity, often studied for its potential as a pharmaceutical agent or in biochemical research. The presence of chlorine atoms can influence its reactivity and interaction with biological systems, making it a subject of interest in medicinal chemistry. Additionally, its structural features may contribute to its ability to act as a ligand or inhibitor in various enzymatic processes. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.
Formula:C12H8Cl2N4
InChI:InChI=1S/C12H8Cl2N4/c13-10-9-11(17-12(14)16-10)15-7-18(9)6-8-4-2-1-3-5-8/h1-5,7H,6H2
InChI key:InChIKey=XRCTVEFABOUQNI-UHFFFAOYSA-N
SMILES:C(N1C=2C(N=C1)=NC(Cl)=NC2Cl)C3=CC=CC=C3
Synonyms:- 2,6-Dichloro-7-(phenylmethyl)-7H-purine
- 7-Benzyl-2,6-dichloropurine
- Purine, 7-benzyl-2,6-dichloro-
- 2,6-Dichloro-7-benzylpurine
- 7H-Purine, 2,6-dichloro-7-(phenylmethyl)-
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Found 4 products.
7-Benzyl-2,6-dichloro-7H-purine
CAS:Formula:C12H8Cl2N4Purity:95%Color and Shape:SolidMolecular weight:279.12477-benZyl-2,6-dichloro-7h-purine
CAS:7-benZyl-2,6-dichloro-7h-purinePurity:97%Molecular weight:279.12g/mol7-Benzyl-2,6-dichloro-7H-purine
CAS:<p>7-Benzyl-2,6-dichloro-7H-purine is a reagent that is used in the synthesis of adenine and other purines. It can be synthesized by coupling 3-methylxanthine with aminoacids and organometallic reagents. This chemical can also be used to selectively synthesize 6-benzyladenine, which is an important precursor to pharmaceuticals. The 7-benzyl group on this chemical has been shown to act as a positional group in the catalytic hydrogenation of amines. This selective hydrogenation process has been found to be regioselective for cycloalkyl amines.</p>Formula:C12H8Cl2N4Purity:Min. 95%Molecular weight:279.1 g/mol



