BRL 49653

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Identification

Molecular formula
C13H13BrN6
CAS Number
130806-84-5
IUPAC Name
1-(4-bromophenyl)-2-(4,6-dimethylpyrimidin-2-yl)guanidine
Molecular Weight
375.19g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3885g/cm3
Synonyms
Cambridge id 5804741
Interesting facts

Exploring 1-(4-bromophenyl)-2-(4,6-dimethylpyrimidin-2-yl)guanidine

The compound 1-(4-bromophenyl)-2-(4,6-dimethylpyrimidin-2-yl)guanidine is a fascinating substance within the realm of medicinal chemistry. Known for its unique structural features and versatile applications, it plays a critical role in various chemical pathways.

Key Characteristics

  • Pharmacological Relevance: This compound is often analyzed for its potential as a pharmacological agent. Its intricate design allows for interaction with biological targets, making it a significant subject of study in drug development.
  • Structural Insights: The addition of bromine in the phenyl group enhances the compound's reactivity, providing opportunities for diverse chemical transformations. The pyrimidine moiety contributes additional properties, such as the ability to form hydrogen bonds.
  • Mechanism of Action: Researchers are keenly interested in how this compound interacts at the molecular level, especially regarding its binding affinity and selectivity towards specific receptors.

Applications and Research

This compound's ability to influence biological systems has made it a prime candidate for investigational studies aimed at understanding complex diseases. Some interesting areas of focus include:

  • Investigating its antitumor properties, particularly in relation to inhibiting cancer cell proliferation.
  • Exploring its role in modulating neurotransmitter systems, which could provide insights into treating neurological disorders.
  • Evaluating its effectiveness as a biochemical tool for studying enzyme activity and function.

"The beauty of chemical compounds lies not only in their structure but in their potential to shape our understanding of complex biological systems."

In summary, 1-(4-bromophenyl)-2-(4,6-dimethylpyrimidin-2-yl)guanidine stands out as a compound of considerable interest, bridging the gap between synthetic chemistry and its applications in pharmacology. The ongoing research surrounding this compound promises to uncover even more intriguing possibilities.

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