20917-99-1

Basic information

• Product Name: 2,7-Decahydronaphthalenediol
• Synonyms: 2,7-Decahydronaphthalenediol;Decahydro-2,7-Naphthalenediol
• CAS NO: 20917-99-1
• Molecular Formula: C10H18O2
• Molecular Weight: 170.25
• Mol File: 20917-99-1.mol

Chemical Properties

• Boiling Point: 321.2 °C at 760 mmHg
• Flash Point: 156.4 °C
• Appearance: /
• Density: 1.117 g/cm³
• Vapor Pressure: 2.44E-05mmHg at 25°C
• Refractive Index: 1.533
• CAS DataBase Reference: 2,7-Decahydronaphthalenediol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,7-Decahydronaphthalenediol(20917-99-1)
• EPA Substance Registry System: 2,7-Decahydronaphthalenediol(20917-99-1)

Safety Data

• Hazardous Substances Data: 20917-99-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2,7-Decahydronaphthalenediol is used as a key intermediate compound for the synthesis of potential decalindiones. These decalindiones can be utilized as substrates in the study of horse liver alcohol dehydrogenase, an enzyme that plays a crucial role in the metabolism of alcohols.
Used in Chemical Synthesis:
2,7-Decahydronaphthalenediol is used as a building block in the synthesis of various chemical compounds, particularly those with complex molecular structures. Its unique properties make it a valuable component in the development of new materials and products.
Used in Research and Development:
Due to its unique structure and properties, 2,7-Decahydronaphthalenediol is employed in research and development for exploring its potential applications in various fields, such as pharmaceuticals, materials science, and chemical engineering. It can serve as a starting point for the development of new drugs, materials, or chemical processes.

InChI:InChI=1/C10H18O2/c11-9-3-1-7-2-4-10(12)6-8(7)5-9/h7-12H,1-6H2

Upstream product

• 582-17-2 2,7-Dihydroxynaphthalene 
• 111219-19-3 C₁₇H₂₂N₂O₂S 
• 111219-11-5 trans-bicyclo<4.4.0>dec-8-en-3-one 

Relevant articles and documents

Spirocyclic Nitroxide Biradicals: Synthesis and Evaluation as Dynamic Nuclear Polarizing Agents

A method for the synthesis of rigid nitroxide biradicals with various spatial orientations between the radical centers is reported. Diketones were employed as substrates for tin amine protocol (SnAP) reagents to provide the parent spirocyclic diamines. Oxidation by peroxyacids provided the corresponding nitroxide biradicals. A set of four different biradicals with various interelectron distances and torsion angles between the radical planes was synthesized using this method. The exact geometries were determined by X-ray crystallography and the biradicals were investigated by EPR spectroscopy and evaluated for their dynamic nuclear polarization (DNP) performance. 1H-DNP enhancements in the range of 1.2–2.1 at 14.1 Tesla (600 MHz spectrometer) were achieved. This synthetic methodology opens a promising alternative to access nitroxide biradicals with various torsional angles and inter radical distances.

Enzymes in organic synthesis. 37. Preparation and characterization of potential decalindione substrates of horse liver alcohol dehydrogenase

The preparations of ten decalindiones for investigation as substrates of horse liver alcohol dehydrogenase are reported.The structure characterizations include clarifications of some ambiguities in the decalin literature.