4-Iodobenzothiophene-2-carboxamidine
ADVERTISEMENT
- Molecular formula
- C9H7INS
- CAS Number
- 74209-19-1
- IUPAC Name
- 4-iodobenzothiophene-2-carboxamidine
- Molecular Weight
- 291.12g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.9000g/cm3
- Synonyms
- 4-iodo-1-benzothiophene-2-carboximidamide
Identification
Interesting facts
Interesting Facts about 4-Iodobenzothiophene-2-carboxamidine
4-Iodobenzothiophene-2-carboxamidine is an intriguing chemical compound that presents a diverse range of applications and features in the field of chemistry. Here are some noteworthy aspects:
- Unique Structure: This compound consists of a benzothiophene core, which is a fused ring system incorporating both sulfur and carbon atoms. This structural complexity contributes to its distinct chemical properties.
- Diverse Applications: 4-Iodobenzothiophene-2-carboxamidine can be utilized in various scientific fields including organic synthesis, materials science, and pharmaceuticals. Its ability to participate in cross-coupling reactions makes it valuable for synthesizing more complex molecules.
- Research Potential: This compound has attracted attention for its potential biological activity. Research studies suggest it may have applications in developing new pharmacological agents targeting specific diseases.
- Synthetic Versatility: The presence of both iodine and the carboxamidine functional group provides chemists with unique reactivity options, enabling the formation of multiple products through various organic reactions.
- Environmental Considerations: As research continues, understanding the environmental impact of compounds such as 4-iodobenzothiophene-2-carboxamidine becomes increasingly important. This includes studying its stability and degradation pathways.
In conclusion, the versatility and unique properties of 4-iodobenzothiophene-2-carboxamidine offer exciting opportunities for further research and application in numerous scientific domains. Its potential to contribute to innovative solutions in chemistry exemplifies the dynamic nature of chemical study.