Cas no 3716-38-9 (Octahydro-1H-inden-5-ol (Mixture of Diastereomers))

Octahydro-1H-inden-5-ol (mixture of diastereomers) is a saturated bicyclic alcohol with potential applications in organic synthesis and fragrance chemistry. Its rigid indane backbone and hydroxyl functionality make it a versatile intermediate for the preparation of complex molecules, including pharmaceuticals and fine chemicals. The mixture of diastereomers offers flexibility in stereochemical exploration, enabling tailored synthetic routes. The compound's stability and moderate reactivity allow for selective derivatization under controlled conditions. Its structural features may also contribute to unique olfactory properties, making it of interest in flavor and fragrance formulations. The product is typically supplied with high purity, ensuring reproducibility in research and industrial applications.
Octahydro-1H-inden-5-ol (Mixture of Diastereomers) structure
3716-38-9 structure
Product Name:Octahydro-1H-inden-5-ol (Mixture of Diastereomers)
CAS No:3716-38-9
MF:C9H16O
MW:140.222743034363
CID:315509
PubChem ID:228142
Update Time:2025-05-20

Octahydro-1H-inden-5-ol (Mixture of Diastereomers) Chemical and Physical Properties

Names and Identifiers

    • 1H-Inden-5-ol,octahydro-
    • 2,3,3a,4,5,6,7,7a-octahydro-1H-inden-5-ol
    • (+-)-(3ar,7at)-Hexahydro-indan-5t-ol
    • AC1L5G0A
    • AC1Q7AHE
    • AC1Q7B0N
    • AR-1K8885
    • HEXAHYDROINDAN-5-OL
    • NSC20778
    • octahydro-1h-inden-5-ol
    • SureCN9909854
    • CS-0233495
    • 3716-38-9
    • DTXSID00281216
    • Octahydro-1H-inden-5-ol (Mixture of Diastereomers)
    • SCHEMBL9909854
    • HEXAHYDRO-5-INDANOL,TECH.
    • AKOS006274800
    • NSC-20778
    • EN300-134020
    • SB85138
    • Inchi: 1S/C9H16O/c10-9-5-4-7-2-1-3-8(7)6-9/h7-10H,1-6H2
    • InChI Key: IGRYUSXMPCQPHK-UHFFFAOYSA-N
    • SMILES: OC1CCC2CCCC2C1

Computed Properties

  • Exact Mass: 140.12018
  • Monoisotopic Mass: 140.12
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 0
  • Complexity: 122
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 3
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.4
  • Topological Polar Surface Area: 20.2?2

Experimental Properties

  • Density: 1.018
  • Boiling Point: 229°Cat760mmHg
  • Flash Point: 93.3°C
  • Refractive Index: 1.509
  • PSA: 20.23
  • LogP: 1.94750

Octahydro-1H-inden-5-ol (Mixture of Diastereomers) Pricemore >>

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Additional information on Octahydro-1H-inden-5-ol (Mixture of Diastereomers)

Octahydro-1H-inden-5-ol (Mixture of Diastereomers): A Comprehensive Overview

Octahydro-1H-inden-5-ol, also known by its CAS number CAS No. 3716-38-9, is a versatile compound with a rich history in organic chemistry and various industrial applications. This compound, which exists as a mixture of diastereomers, has garnered significant attention due to its unique structural properties and potential in diverse fields such as pharmaceuticals, agrochemicals, and materials science.

The structure of Octahydro-1H-inden-5-ol is characterized by a bicyclic framework with a hydroxyl group at the 5-position. This configuration imparts the molecule with stereochemical complexity, leading to the formation of diastereomeric mixtures. Recent advancements in stereochemistry have enabled researchers to better understand the synthesis and separation of these diastereomers, paving the way for more precise applications in drug design and catalysis.

One of the most notable aspects of CAS No. 3716-38-9 is its role as an intermediate in the synthesis of complex natural products and bioactive molecules. For instance, studies have shown that this compound can serve as a key building block in the construction of terpenoids and other polyketide-derived compounds. Its ability to undergo various transformations, including oxidation, reduction, and cyclization reactions, makes it an invaluable tool in organic synthesis.

Recent research has also highlighted the potential of Octahydro-1H-inden-5-ol in the development of novel chiral catalysts. By leveraging its inherent chirality, scientists have successfully employed this compound in asymmetric catalysis, leading to the enantioselective synthesis of high-value pharmaceutical intermediates. These findings underscore the importance of understanding the stereochemical properties of such compounds in advancing modern chemical synthesis.

In addition to its synthetic applications, CAS No. 3716-38-9 has found utility in materials science, particularly in the development of advanced polymers and composites. Its unique physical properties, such as thermal stability and mechanical strength, make it a promising candidate for use in high-performance materials. Ongoing studies are exploring its potential as a precursor for biodegradable polymers, aligning with current trends toward sustainable materials development.

The production of Octahydro-1H-inden-5-ol involves a variety of synthetic routes, each offering distinct advantages depending on the desired scale and purity requirements. Traditional methods often rely on catalytic hydrogenation or ring-opening reactions, while modern approaches incorporate green chemistry principles to enhance efficiency and reduce environmental impact.

In conclusion, CAS No. 3716-38-9, or Octahydro-1H-inden-5-o, stands as a testament to the ingenuity and progress in organic chemistry. Its diverse applications and ongoing research highlight its significance as a multifaceted compound with vast potential across various industries.

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