N-(4-carbamimidoyl-3-chloro-phenyl)-2-hydroxy-3-iodo-5-methyl-benzamide
- Molecular formula
- C16H14ClIN3O2
- CAS Number
- 123456-78-9
- IUPAC Name
- N-(4-carbamimidoyl-3-chloro-phenyl)-2-hydroxy-3-iodo-5-methyl-benzamide
- Molecular Weight
- 420.99g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 2.1000g/cm3
- Appearance
- may range from a pale yellow to white, depending on the purity and specific synthesis conditions. In some cases, it may also appear slightly beige due to the presence of trace impurities. The crystalline structure may be observed under a microscope, showcasing defined edges and facets.
- Synonyms
- n-(4-carbamimidoyl-3-choro-phenyl)-2-hydroxy-3-iodo-5-methyl-benzamide
Identification
Interesting Facts about N-(4-carbamimidoyl-3-chloro-phenyl)-2-hydroxy-3-iodo-5-methyl-benzamide
N-(4-carbamimidoyl-3-chloro-phenyl)-2-hydroxy-3-iodo-5-methyl-benzamide is a fascinating compound with numerous applications in the field of medicinal chemistry and pharmaceuticals. This intricate molecule is characterized by its unique combination of functional groups, which bestow upon it interesting biological properties.
Key Highlights:
- Diverse Biological Activity: This compound is part of a class of molecules that are often investigated for their potential pharmacological effects, particularly in acting as inhibitors or modulators of various biological pathways.
- Structural Complexity: The presence of multiple heavy atoms such as iodine and chlorine makes this compound particularly intriguing for studies involving organohalogen chemistry and its perturbative effect on biological systems.
- Applications in Drug Development: Compounds like this are often explored for their potential roles in treating diseases, particularly in targeting specific enzymes or receptors in therapeutic areas.
- Synthetic Challenges: The synthesis of this compound can present unique challenges, especially in achieving the desired selectivity and yield due to its complex structure, making it an interesting case study for synthetic chemists.
Moreover, as a research chemist or a student exploring new compounds, one might find it captivating to analyze the reactivity patterns of the functional groups present in N-(4-carbamimidoyl-3-chloro-phenyl)-2-hydroxy-3-iodo-5-methyl-benzamide. Each substituent can influence the molecule’s overall behavior, affecting not only its stability but also its interaction with biological macromolecules.
As noted by chemists in the field, "The specificity of a compound often lies in its structure, and understanding these relationships paves the way for innovative drug design." This quote underscores the significance of compounds like this in the broader scope of medicinal chemistry.
In conclusion, N-(4-carbamimidoyl-3-chloro-phenyl)-2-hydroxy-3-iodo-5-methyl-benzamide stands out as a compound worthy of exploration, embodying the journey of discovery present in the world of chemical research.