CAS 5470-24-6

6-Chloro-9-phenyl-9H-purine

Description:

6-Chloro-9-phenyl-9H-purine is a purine derivative characterized by the presence of a chlorine atom at the 6-position and a phenyl group at the 9-position of the purine ring. This compound exhibits properties typical of purines, including potential biological activity, as purines are fundamental components of nucleic acids and play crucial roles in cellular processes. The chlorine substituent can influence the compound's reactivity and solubility, while the phenyl group may enhance lipophilicity, affecting its interaction with biological membranes. 6-Chloro-9-phenyl-9H-purine may also exhibit pharmacological properties, making it of interest in medicinal chemistry and drug development. Its molecular structure allows for various chemical reactions, including substitution and coupling, which can be exploited in synthetic applications. As with many chemical substances, safety and handling precautions should be observed, as the biological effects and toxicity profiles of such compounds can vary significantly.

Formula: C₁₁H₇ClN₄

InChI: InChI=1S/C11H7ClN4/c12-10-9-11(14-6-13-10)16(7-15-9)8-4-2-1-3-5-8/h1-7H

InChI key: InChIKey=MNWAWPZGZXXLBU-UHFFFAOYSA-N

SMILES: ClC1=C2C(N(C=N2)C3=CC=CC=C3)=NC=N1

Synonyms:

• 6-Chloro-9-phenyl-9H-purine
• 6-Chloro-9-phenylpurine
• 9H-Purine, 6-chloro-9-phenyl-
• NSC 26291

6-Chloro-9-phenyl-9H-purine

CAS: 5470-24-6

Formula: C₁₁H₇ClN₄

Purity: 95%

Color and Shape: Solid

Molecular weight: 230.6531

Ref: IN-DA00E14P

6-Chloro-9-phenyl-9H-purine

CAS: 5470-24-6

6-Chloro-9-phenyl-9H-purine

Purity: 95%

Molecular weight: 230.66g/mol

Ref: 54-OR1072205

6-Chloro-9-phenyl-9H-purine

CAS: 5470-24-6

Formula: C₁₁H₇ClN₄

Color and Shape: Neat

Molecular weight: 230.653

Ref: TR-C995383

6-Chloro-9-phenyl-9H-purine

CAS: 5470-24-6

6-Chloro-9-phenyl-9H-purine is an antipurinic agent that inhibits the production of nucleic acids. It is a derivative of 6,6'-dichloro-2,2'-diimidazole and is used as a precursor in the synthesis of other analogues. The yield of this compound can be increased by using carbon tetrachloride as a catalyst. 6-Chloro-9-phenyl-9H-purine has been shown to be an effective catalyst for imidazolium and benzimidazolium salts. This compound also exhibits nucleophilic properties which may be due to the dipole moment created by the nitrogen atom on one side and the oxygen atom on the other side.

Formula: C₁₁H₇ClN₄

Purity: Min. 95%

Molecular weight: 230.65 g/mol

Ref: 3D-FAA47024