Interesting facts
              Discovering 3-(2-hydroxyethyl)-1H-indol-5-ol
3-(2-hydroxyethyl)-1H-indol-5-ol, often referred to simply as a derivative of indole, is a fascinating compound with significant implications in various domains of science. Here are some interesting facts about this intriguing compound:
- Indole Structure: Indole compounds are known for their aromatic character and essential role in biological systems. The indole structure is the foundation for numerous naturally occurring alkaloids.
- Biological Activity: Compounds derived from indole structures often exhibit diverse biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. 3-(2-hydroxyethyl)-1H-indol-5-ol is no exception and may offer similar therapeutic potentials.
- Research Applications: This compound is of great interest in medicinal chemistry and pharmacology. Scientists are continually exploring how modifications to the indole backbone can enhance its biological efficacy.
- Importance in Natural Products: Indole derivatives are prevalent in many natural products. Their derivatives often serve as precursors to critical biological molecules, including neurotransmitters and hormones.
- Versatility: The presence of a hydroxyethyl group contributes to the compound's solubility and reactivity, enabling a range of synthetic pathways for chemists aiming to develop new compounds.
As more is understood about the properties and potential applications of 3-(2-hydroxyethyl)-1H-indol-5-ol, it could unlock new frontiers in drug discovery and development. The indole’s enigmatic nature continues to captivate researchers and students alike, marking it as a significant compound in the world of organic chemistry.
Synonyms
          5-Hydroxytryptophol
          154-02-9
          3-(2-Hydroxyethyl)-1H-indol-5-ol
          Hydroxytryptophol
          5-Hydroxy-1H-indole-3-ethanol
          5-Hydroxy Tryptophol
          5-Hydroxyindole-3-ethanol
          1H-Indole-3-ethanol, 5-hydroxy-
          INDOLE-3-ETHANOL, 5-HYDROXY-
          EINECS 205-820-4
          NSC 84416
          BRN 0143517
          52MNE52QA1
          NSC-84416
          TRYPTOPHOL, 5-HYDROXY-
          DTXSID80165505
          4-21-00-02181 (Beilstein Handbook Reference)
          5-hydroxy-3-(2-hydroxyethyl)indole
          5-HYDROXYINDOLE-3-(2-HYDROXY)ETHYL
          MFCD00047197
          5-hydroxyindolacetate
          5-hydroxyindoacetic acid
          5-HTOL
          5-hydroxyindole-acetic acid
          UNII-52MNE52QA1
          5-hydroxy-indole-acetic acid
          SCHEMBL233744
          DTXCID5087996
          CHEBI:89825
          KQROHCSYOGBQGJ-UHFFFAOYSA-
          BDBM428840
          NSC84416
          5-hydroxy-3-(2-hydroxyethyl)-indole
          AKOS004911590
          3-(2-hydroxy-ethyl)-1H-indol-5-ol
          5-Hydroxy-1H-Indole-3-ethanol(9CI)
          CS-W021759
          FH24155
          HY-W041019
          3-(2-Hydroxyethyl)-1H-indol-5-ol #
          AS-37867
          PD018434
          US10544152, Cpd # 27
          NS00025004
          Q27162013
          5-Hydroxy-1H-indole-3-ethanol;5-Hydroxy-3-(2-hydroxyethyl)indole;NSC 84416
          205-820-4
          InChI=1/C10H11NO2/c12-4-3-7-6-11-10-2-1-8(13)5-9(7)10/h1-2,5-6,11-13H,3-4H2
              
Solubility of 3-(2-hydroxyethyl)-1H-indol-5-ol
The solubility characteristics of 3-(2-hydroxyethyl)-1H-indol-5-ol can be quite fascinating due to its unique molecular structure. This compound is generally soluble in various solvents, which makes it an interesting subject of study in terms of applications and functionalities.
Key Points on Solubility:
“Understanding the solubility of compounds is crucial for their applications in pharmaceuticals, environmental science, and industrial processes.” Thus, the solubility profile of 3-(2-hydroxyethyl)-1H-indol-5-ol not only offers insights into its behavior in various environments but also dictates its suitability for various uses. Further research can elaborate on how this compound behaves in different physical and chemical landscapes, opening doors to innovative applications.