646510-36-3

Usage

Explanation

The compound consists of 12 carbon atoms, 8 hydrogen atoms, 2 chlorine atoms, 4 nitrogen atoms, and 1 sulfur atom.
2. Purine derivative

Explanation

It is a modified version of the naturally occurring purine, a heterocyclic organic compound found in various biological systems.
3. Purine ring structure

Explanation

The compound contains a purine ring, which is a double-ring structure consisting of a six-membered pyrimidine ring fused to a five-membered imidazole ring.
4. Chlorine atom at the 2 position

Explanation

One of the two chlorine atoms is attached to the carbon atom at the 2nd position of the purine ring, which influences the compound's properties and reactivity.
5. Phenylthio group at the 6 position

Explanation

A phenylthio group (a benzene ring with a sulfur atom attached) is present at the 6th position of the purine ring, further affecting the compound's properties and reactivity.
6. Potential pharmaceutical applications

Explanation

Due to its structural similarity to other purine-based compounds with various biological activities, it may have potential applications in pharmaceutical research.
7. Anticancer and antiviral properties

Explanation

Some purine-based compounds exhibit anticancer and antiviral properties, making 1H-Purine, 2-chloro-6-[(4-chlorophenyl)thio]- a potential candidate for further research in these areas.
8. Unknown pharmacological and toxicological properties

Explanation

The specific pharmacological and toxicological properties of 1H-Purine, 2-chloro-6-[(4-chlorophenyl)thio]- are yet to be fully elucidated, requiring further research to understand its potential applications and safety.
9. Need for further research

Explanation

More studies are needed to fully understand the compound's potential applications, efficacy, and safety in various biological contexts.