7-methyl-6-phenylmethoxy-1H-indole
Names and Identifiers of 7-methyl-6-phenylmethoxy-1H-indole
CAS Number |
1000343-99-6 |
|---|---|
IUPAC Name |
7-methyl-6-phenylmethoxy-1H-indole |
Canonical SMILES |
CC1=C(C=CC2=C1NC=C2)OCC3=CC=CC=C3 |
Physical and chemical properties of 7-methyl-6-phenylmethoxy-1H-indole
Boiling Point |
412.5±30.0 °C at 760 mmHg |
|---|---|
Density |
1.2±0.1 g/cm3 |
Exact Mass |
237.115356 |
Flash Point |
149.2±14.8 °C |
Index of Refraction |
1.656 |
LogP |
4.11 |
Molecular Formula |
C16H15NO |
Molecular Weight |
237.296 |
PSA |
25.02000 |
Vapour Pressure |
0.0±0.9 mmHg at 25°C |
Applications of 7-methyl-6-phenylmethoxy-1H-indole
6-(Benzyloxy)-7-methyl-1H-indole serves as an important intermediate in organic synthesis, particularly for creating more complex indole derivatives. Its reactive sites allow for further functionalization, which is valuable in developing pharmaceuticals and other biologically active compounds. Additionally, its unique structure may contribute to novel applications in materials science and chemical biology.
Interaction Studies of 7-methyl-6-phenylmethoxy-1H-indole
Interaction studies involving 6-(benzyloxy)-7-methyl-1H-indole focus on its binding properties with various proteins and enzymes. These studies help elucidate its mechanism of action and potential therapeutic effects. Research has indicated that the compound can modulate enzyme activity, which may lead to significant physiological effects relevant to drug development.
Biological Activity of 7-methyl-6-phenylmethoxy-1H-indole
The biological activity of 6-(benzyloxy)-7-methyl-1H-indole is linked to its interaction with various molecular targets. The benzyloxy group enhances binding affinity to certain enzymes and receptors, potentially modulating their activity. Studies indicate that this compound may have inhibitory or activating effects on various biological pathways, suggesting its utility in pharmacological applications.