Interesting facts
              Interesting Facts about 3-(1H-indol-3-yl)propanoic Acid
3-(1H-indol-3-yl)propanoic acid is a fascinating compound with intriguing properties and applications. Here are some key points that highlight its significance:
- Biological Activity: This compound is known for its potential biological activities, making it a subject of research in pharmacology. It exhibits properties that may influence various biochemical pathways, which could lead to therapeutic applications.
 - Structure and Aesthetics: The unique structure of this compound, featuring an indole moiety, is not only essential for its biological functions but also contributes to its visual identification in molecular modeling.
 - Indole Derivatives: Belonging to the family of indole derivatives, 3-(1H-indol-3-yl)propanoic acid can serve as a starting material in synthesizing various dye and drug compounds. Indoles, in general, are a significant class of heterocyclic compounds found widely in nature.
 - Research Potential: Studies have suggested that compounds like 3-(1H-indol-3-yl)propanoic acid may possess antidepressant effects, potentially aiding in the development of new treatments for mood disorders.
 - Impact on Neurotransmission: Due to the structural similarity to neurotransmitters, this compound may interact with neural receptors, enhancing our understanding of the chemistry behind neural signaling.
 
Overall, 3-(1H-indol-3-yl)propanoic acid holds promise not just in academic research but also in medicinal chemistry. Its potential applications and biological significance open doors for future investigations, enriching the scientific community's knowledge base.
Synonyms
          3-Indolepropionic acid
          830-96-6
          Indole-3-propionic acid
          3-(1H-Indol-3-yl)propanoic acid
          1H-Indole-3-propanoic acid
          Indolepropionic acid
          3-(3-Indolyl)propionic acid
          3-(3-Indolyl)propanoic acid
          Indolylpropionic Acid
          IPA (auxin)
          3-(Indol-3-yl)propionic acid
          1H-INDOLE-3-PROPIONIC ACID
          3-(3-Indole)propionic acid
          Oxigon
          beta-Indolylpropionate
          3-(2-Carboxyethyl)-1H-indole
          3-Indolepropionicacid
          indole propionate
          indole-3-propanoic acid
          MFCD00005660
          beta-(3-Indolyl)propionic acid
          NSC 3252
          1H-Indole-3-proponoic acid
          NSC 47831
          CCRIS 4424
          3-(Indol-3-yl)propanoic acid
          3-(1H-Indol-3-yl)propionic acid
          EINECS 212-600-1
          JF49U1Q7KN
          BRN 0147733
          VP-20629
          CHEBI:43580
          AI3-17433
          NSC-3252
          3-(1H-indol-3-yl)-propionic acid
          NSC-47831
          .beta.-Indolepropionic acid
          VP 20629
          .beta.-Indole-3-propionic acid
          DTXSID7061192
          .beta.-(3-Indolyl)propionic acid
          5-22-03-00114 (Beilstein Handbook Reference)
          .beta.-Indolylpropionate
          3-(1H-Indol-3-yl)propionate
          UNII-JF49U1Q7KN
          b-Indolepropionate
          4ejl
          3-Indolepropionate
          Indole-3-propionic
          beta-Indolepropionate
          3-indolpropionic acid
          b-Indolepropionic acid
          b-Indole-3-propionate
          Acid, 7
          3-Indole propionic acid
          Indole 3-propionic acid
          1H-Indole-3-propionate
          beta-Indolepropionic acid
          indole-3-proprionic acid
          b-(3-Indolyl)propionate
          beta-Indole-3-propionate
          Maybridge1_002431
          3-(3-Indolyl)propanoate
          3-(3-Indolyl)propionate
          b-Indole-3-propionic acid
          beta-(3-Indolyl)propionate
          Oprea1_071255
          b-(3-Indolyl)propionic acid
          beta-Indole-3-propionic acid
          BIDD:GT0788
          DivK1c_001183
          SCHEMBL195405
          3-Indolepropionic acid (IPA)
          3-(3-indolyl)-propionic acid
          CHEMBL207225
          GTPL4709
          SCHEMBL1767754
          SHP622
          DTXCID5048342
          BDBM31879
          HMS548G11
          NSC3252
          SHP-622
          1F1-N
          3-Indolepropionic acid (Standard)
          GLXC-03350
          HMS3604I20
          HMS3886E03
          ALBB-034983
          BCP26573
          HY-W015229R
          NSC47831
          BBL001406
          s4809
          STK247053
          3-(1H-Indol-3-yl)propanoic acid #
          AKOS000120911
          CCG-115418
          CS-W015945
          DB02758
          FI30477
          FS-3158
          HY-W015229
          SDCCGMLS-0065895.P001
          VP20629
          CDS1_000143
          NCGC00340705-01
          AC-10570
          BP-21044
          SY015400
          DB-011207
          Indole-3-propionic acid, >=97.0% (T)
          Indole-3-propionic acid, >=99.0% (T)
          I0032
          NS00038237
          EN300-20789
          3-Indolepropionic acid, ReagentPlus(R), 99%
          C22236
          AB01333057-02
          BRD-K21071223-001-02-8
          Q21098993
          3-Indolepropionic acid, Vetec(TM) reagent grade, 99%
          F0849-0388
          Z104482518
          10265-77-7
          212-600-1
              
Solubility of 3-(1H-indol-3-yl)propanoic acid
3-(1H-indol-3-yl)propanoic acid, with the chemical formula C11H11NO2, exhibits interesting solubility characteristics. Understanding the solubility of this compound can be essential for its applications in various fields, including pharmaceuticals and research. Here are some key points regarding its solubility:
In summary, the solubility of 3-(1H-indol-3-yl)propanoic acid is significantly influenced by its chemical structure, specifically the balance between its polar and non-polar regions. For optimal use, it is crucial to consider these solubility properties when selecting solvents for experiments or formulations.