Interesting facts
Interesting Facts About 2-amino-4-(1H-indol-5-yl)buta-1,3-diene-1,1,3-tricarbonitrile
This compound, also known as a versatile intermediate in organic synthesis, has caught the attention of scientists due to its intriguing structure and potential applications. Here are some fascinating aspects:
- Structure and Functionality: The presence of the indole moiety is significant as it forms the backbone for many biologically active compounds. Indoles are known for their role in various natural products, including hormones, neurotransmitters, and alkaloids.
- Biological Relevance: Given its structure, 2-amino-4-(1H-indol-5-yl)buta-1,3-diene-1,1,3-tricarbonitrile has potential implications in medicinal chemistry. Compounds with similar frameworks have been associated with activity against diseases such as cancer and bacterial infections.
- Reactivity: The tricarbonitrile functional groups contribute to its reactivity, allowing for various chemical transformations. It's not uncommon for compounds like this to participate in cycloaddition reactions, which can yield diverse products.
- Research Opportunities: Many researchers are drawn to this compound for exploration in material science. The ability to modify the structure can lead to the development of new materials with desirable electronic or optical properties.
- Synthetic Pathways: The synthesis of such compounds often involves intricate multi-step processes, which provide ample room for the creativity of chemists. Understanding these pathways can lead to more efficient synthetic methodologies.
As stated by notable chemist Linus Pauling, “The best way to have a good idea is to have lots of ideas.” Exploring compounds like this one further reinforces this notion within the scientific community, highlighting the continuous pursuit of knowledge and innovation.
In summary, 2-amino-4-(1H-indol-5-yl)buta-1,3-diene-1,1,3-tricarbonitrile exemplifies the intersection of structure and function in chemistry, opening doors for both research and application in multiple scientific disciplines.
Synonyms
2-amino-4-(1H-indol-5-yl)buta-1,3-diene-1,1,3-tricarbonitrile
133550-06-8
134036-53-6
Tyrphostin AG 370
CBiol_001925
KBioGR_000114
KBioGR_000534
KBioSS_000114
KBioSS_000534
SCHEMBL2956923
KBio2_000114
KBio2_000534
KBio2_002682
KBio2_003102
KBio2_005250
KBio2_005670
KBio3_000227
KBio3_000228
KBio3_000967
KBio3_000968
DTXSID40274349
Bio1_000211
Bio1_000700
Bio1_001189
Bio2_000114
Bio2_000437
Bio2_000594
Bio2_000917
1,3-Butadiene-1,1,3-tricarbonitrile,2-amino-4-(1H-indol-5-yl)-,(Z)
SMP1_000116
NCI60_018062
Q27164300
Solubility of 2-amino-4-(1H-indol-5-yl)buta-1,3-diene-1,1,3-tricarbonitrile (C18H9N3)
The solubility of 2-amino-4-(1H-indol-5-yl)buta-1,3-diene-1,1,3-tricarbonitrile is influenced by several factors due to its complex structure. This compound, characterized by its nitrogen-rich content and unique indole moiety, typically shows a range of solubility behaviors in various solvents.
Factors Affecting Solubility:
However, it is essential to note that the solubility may vary significantly with the solvent choice, as non-polar solvents like hexane might not dissolve this compound effectively due to its polar functionalities. As a rule of thumb in chemistry, “like dissolves like,” implying that polar compounds dissolve well in polar solvents while non-polar compounds favor non-polar environments.
In summary, while the solubility of C18H9N3 can be favorable in specific conditions, it requires careful consideration of the solvent's properties to optimize dissolution.