Interesting facts
              Interesting Facts about 3-[(Dimethylamino)methyl]-1H-indole-5-carbonitrile
This compound is categorized as an indole derivative, which means it contains the indole structure, a bicyclic compound constituted as a fused benzene and pyrrole ring. Indoles are significant in organic chemistry and biology due to their presence in various natural compounds, pharmaceuticals, and agrochemicals.
Key Features of 3-[(Dimethylamino)methyl]-1H-indole-5-carbonitrile:
- Versatile Intermediates: The compound serves as a versatile building block in the synthesis of more complex molecules, particularly in drug discovery and development.
 - Biological Activity: Compounds containing indoles often exhibit a wide spectrum of biological properties, including anticancer, antimicrobial, and anti-inflammatory activities. This makes them essential in medicinal chemistry.
 - Functional Group Influence: The presence of the dimethylamino group enhances the compound's basicity, which can influence its reactivity and interactions in biological systems.
 - Synthetic Pathways: It can be synthesized through various methods, including the manipulation of existing indole derivatives to introduce the dimethylamino and carbonitrile functional groups.
 
As you delve deeper into the study of this compound, consider how the symbiotic relationship between its structure and reactivity contributes to its utility in both academic research and industrial applications. With indole derivatives like this one, the potential for innovation in pharmacology and materials science is immense. Engaging with such compounds broadens the understanding of structure-property relationships in chemistry.
Synonyms
          5-Cyanogramine
          25514-67-4
          3-(Dimethylaminomethyl)indole-5-carbonitrile
          DTXSID30180203
          1H-Indole-5-carbonitrile, 3-((dimethylamino)methyl)-
          1H-Indole-5-carbonitrile, 3-[(dimethylamino)methyl]-
          INDOLE-5-CARBONITRILE, 3-(DIMETHYLAMINOMETHYL)-
          RefChem:302709
          DTXCID00102694
          1H-Indole-5-carbonitrile, 3-((dimethylamino)methyl)-(9CI)
          3-((dimethylamino)methyl)-1H-indole-5-carbonitrile
          3-[(dimethylamino)methyl]-1H-indole-5-carbonitrile
          MFCD01719098
          SCHEMBL4358526
          JOPBIDDQPQFQHZ-UHFFFAOYSA-N
          AKOS005259084
          AC-27829
          BS-27730
          5-cyano-3-(dimethylamino)methyl-1H-indole
          DB-021554
          CS-0210222
          514C674
          F471220
              
Solubility of 3-[(dimethylamino)methyl]-1H-indole-5-carbonitrile
The solubility of 3-[(dimethylamino)methyl]-1H-indole-5-carbonitrile can be influenced by several factors, including its molecular structure, polarity, and the solvent used. Here are some key points to consider:
Solubility does not follow a one-size-fits-all rule, and empirical testing is often necessary to determine how well 3-[(dimethylamino)methyl]-1H-indole-5-carbonitrile dissolves in a given solvent. As noted in various studies, the solubility data can vary from moderate to high in organic solvents, suggesting that it is essential to consider the specific application when choosing a solvent for this compound.
Overall, understanding the solubility of this compound is crucial for its applications in synthesis and formulation.