Interesting facts
              Interesting Facts about Indan-1-one
Indan-1-one is a fascinating compound that belongs to the family of ketones and is characterized by its unique bicyclic structure. It is renowned for several interesting properties and applications in various fields:
- Structure and Stability: The compound features a cyclic alkyl group fused to a carbonyl group. This unique structure contributes to its stability and makes it of interest in synthetic chemistry.
 - Biological Activity: Indan-1-one and its derivatives have shown promising biological activities, including anti-inflammatory and analgesic effects. Research is ongoing to explore its potential as a therapeutic agent.
 - Applications in Organic Synthesis: Indan-1-one is employed as an intermediate in the synthesis of various pharmaceuticals and fine chemicals. Its versatility allows chemists to create diverse molecular architectures.
 - Historical Significance: The discovery of indan-1-one traces back to the early 20th century when its structural features were first elucidated, paving the way for advancements in organic chemistry.
 - Polymer Chemistry: It plays a role in the synthesis of polymers, particularly when functionalized with other groups. Its incorporation into polymeric materials can impart unique physicochemical properties.
 
As highlighted by a notable chemist, "Understanding the intricacies of compounds like indan-1-one can unlock new pathways in drug design and materials science." Thus, exploring indan-1-one not only provides insight into its chemistry but also underlines its relevance in contemporary scientific research.
Synonyms
          1-Indanone
          83-33-0
          2,3-Dihydro-1H-inden-1-one
          Indan-1-one
          INDANONE
          2,3-dihydroinden-1-one
          alpha-Hydrindone
          alpha-Indanone
          1-Indone
          1H-Inden-1-one, 2,3-dihydro-
          Hydrindone
          .alpha.-Indanone
          .alpha.-Hydrindone
          Indanone (VAN)
          MFCD00003785
          2,3-Dihydro-1-indenone
          NSC 2581
          NSC-2581
          EINECS 201-470-1
          1H-INDAN-1-ONE
          V7021Y717I
          1-OXOBENZOCYCLOPENTANE
          AI3-11798
          30286-23-8
          DTXSID1058892
          CHEBI:17404
          RASAGILINE METABOLITE, INDANONE
          Indenone, dihydro-
          1-Hydroindone
          alphaHydrindone
          alphaIndanone
          Indan1one
          1-Ketohydrindene
          1Indone
          indane-1-one
          indanone (1)
          Indanone-(1)
          dihydro-inden-1-one
          2,3Dihydro1Hinden1one
          bmse000496
          1HInden1one, 2,3dihydro
          2,3-dihydro-inden-1-one
          Indan-1-one (1-Indanone)
          SCHEMBL24746
          Indan-1-one, Alpha-Indanone
          SCHEMBL3694431
          DTXCID6048331
          UNII-V7021Y717I
          CHEBI:38132
          NSC2581
          BCP19847
          s9346
          STK290968
          AKOS000119606
          AC-2464
          CCG-321650
          CS-W004333
          FI00120
          HY-W004333
          PB48801
          PS-5770
          1-Indanone, ReagentPlus(R), >=99%
          1-Indanone, purum, >=98.0% (GC)
          BP-12824
          SY001380
          DB-019218
          1-Indanone, Vetec(TM) reagent grade, 98%
          I0013
          NS00038249
          EN300-21403
          C01504
          AH-034/32845037
          Q15906439
          F0001-2126
          Z104495974
          1ON
          201-470-1
              
Solubility of Indan-1-one
Indan-1-one, with the chemical formula C9H8O, is a fascinating compound with notable solubility characteristics. Its ability to dissolve in various solvents is largely influenced by its structure, which includes a carbonyl group that plays a significant role in interactions with solvent molecules.
Solubility Properties:
Overall, the solubility of indan-1-one can be summarized as follows: it is more soluble in organic solvents compared to water, which may be attributed to the hydrophobic characteristics of its aromatic structure. As a general rule, compounds that can engage in hydrogen bonding tend to have improved solubility in polar environments, while those with larger non-polar regions exhibit greater affinity for non-polar solvents. Thus, indan-1-one exemplifies this principle well.