Production Method 1

581-42-0

65051-83-4

496-11-7

573-98-8

569-41-5

527-53-7

575-41-7

767-59-9

620-14-4

2131-42-2

5325-97-3

27133-93-3

3296-50-2

4175-53-5

493-02-7

2039-89-6

629-59-4

1120-21-4

22531-20-0

2234-75-5

Reaction Conditions

1.1 Reagents: Dodecane ,  Decane ,  Tridecane ,  Pentadecane ,  Hydrogen Catalysts: Ruthenium ;  134.1 bar; 3.25 h, 157.6 bar, rt → 305 °C

Reference

An improved catalytic pyrolysis concept for renewable aromatics from biomass involving a recycling strategy for co-produced polycyclic aromatic hydrocarbons

Genuino, Homer C.; Muizebelt, Inouk; Heeres, Andre; Schenk, Niels J.; Winkelman, Jos G. M.; et al, Green Chemistry, 2019, 21(14), 3802-3806

1,2,3,4,5,6,7,8-Octahydrophenanthrene (>85%) Raw materials

• 2,6-Dimethylnaphthalene
• Benzene,(1-methyl-2-cyclopropen-1-yl)-
• Indane
• 1,2-Dimethylnaphthalene
• 1,8-Dimethylnaphthalene
• 1,2,3,5-Tetramethylbenzene
• 1,3-Dimethylnaphthalene
• 1-Methyl-1H-indene
• 3-Ethyltoluene
• Naphthalene,1,4,6-trimethyl-

1,2,3,4,5,6,7,8-Octahydrophenanthrene (>85%) Preparation Products

• 1H-Indene,2,3-dihydromethyl- (27133-93-3)
• 1H-Indene, octahydro-, trans- (3296-50-2)
• 1H-Indene,2,3-dihydro-1,3-dimethyl- (4175-53-5)
• trans-Decahydronaphthalene (493-02-7)
• 1,2,3,4,5,6,7,8-Octahydrophenanthrene (>85%) (5325-97-3)
• 2,5-Dimethylstyrene (stabilized with 4-tert-butylcatechol) (2039-89-6)
• n-Tetradecane (629-59-4)
• Undecane (1120-21-4)
• Naphthalene,6-ethyl-1,2,3,4-tetrahydro- (22531-20-0)
• 1,2,4-Trimethylcyclohexane (2234-75-5)

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• 3. An approach towards the synthesis of novel fused nitrogen tricyclic heterocyclic scaffolds via GBB reaction?
  Sandip Gangadhar Balwe,Yeon Tae Jeong Org. Biomol. Chem., 2018,16, 1287-1296
• 4. An all-solid-state asymmetric device based on a polyaniline hydrogel for a high energy flexible supercapacitor?
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenanthrenes and derivatives Hydrophenanthrenes
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons

Introduction to 1,2,3,4,5,6,7,8-Octahydrophenanthrene (CAS No. 5325-97-3)

1,2,3,4,5,6,7,8-Octahydrophenanthrene (CAS No. 5325-97-3) is a versatile compound with a wide range of applications in the fields of chemistry and materials science. This compound is characterized by its unique molecular structure and properties, making it an essential component in various research and industrial processes. In this article, we will delve into the chemical properties, synthesis methods, and potential applications of 1,2,3,4,5,6,7,8-Octahydrophenanthrene, as well as highlight recent advancements in its study.

Chemical Properties

1,2,3,4,5,6,7,8-Octahydrophenanthrene is a polycyclic aromatic hydrocarbon (PAH) with the molecular formula C₁₄H₁₈. It consists of three fused benzene rings with all hydrogen atoms saturated. The compound is known for its high stability and low reactivity under normal conditions. Its molecular weight is approximately 186.29 g/mol. The physical properties of 1,2,3,4,5,6,7,8-Octahydrophenanthrene include a melting point of around 100-102°C and a boiling point of approximately 300°C at standard pressure. It is insoluble in water but readily dissolves in organic solvents such as ethanol and dichloromethane.

Synthesis Methods

The synthesis of 1,2,3,4,5,6,7,8-Octahydrophenanthrene can be achieved through various routes. One common method involves the hydrogenation of phenanthrene using a suitable catalyst such as palladium on carbon (Pd/C) under high pressure and temperature conditions. Another approach involves the Diels-Alder reaction between a diene and a dienophile followed by hydrogenation to fully saturate the double bonds. Recent advancements in catalytic hydrogenation have led to more efficient and environmentally friendly methods for the synthesis of this compound.

Potential Applications

1,2,3,4,5,6,7,8-Octahydrophenanthrene has found applications in several areas due to its unique properties. In materials science, it serves as a building block for the synthesis of advanced polymers and organic semiconductors. Its saturated structure provides enhanced stability and processability in these materials. In pharmaceutical research, 1,2,3,4,5,6,7,8-Octahydrophenanthrene has been explored as a potential scaffold for drug design due to its ability to form stable complexes with various biological targets.

In the field of organic electronics, 1，2，3，4，5，6，7，8-Octahydrophenanthrene-based materials have shown promise in the development of organic light-emitting diodes (OLEDs) and organic photovoltaic cells (OPVs). The ability to fine-tune the electronic properties of these materials through chemical modification makes them attractive candidates for next-generation electronic devices.

Recent Research Advancements

The scientific community has made significant strides in understanding the behavior and potential applications of 1，2，3，4，5，6，7，8-Octahydrophenanthrene. Recent studies have focused on its use in supramolecular chemistry and self-assembly processes. Researchers have demonstrated that 1，2，3，4，5，6，7，8-Octahydrophenanthrene-based molecules can form well-defined nanostructures through non-covalent interactions such as hydrogen bonding and π-π stacking. These nanostructures have potential applications in drug delivery systems and nanotechnology.

In addition, 1，2，3，4，5，6，7，8-Octahydrophenanthrene-based compounds have been investigated for their photophysical properties. Studies have shown that these compounds exhibit strong fluorescence and can be used as fluorescent probes for biological imaging and sensing applications. The tunable emission properties of 1，2，3，4，5，6，7，8-Octahydrophenanthrene-based fluorophores make them valuable tools in bioanalytical chemistry.

Safety Considerations

Safety is a critical aspect when handling any chemical compound. While 1，2，3，4，5，6，7，8-Octahydrophenanthrene is generally considered safe under normal laboratory conditions, proper handling procedures should always be followed to ensure safety. It is recommended to work with this compound in a well-ventilated area and use appropriate personal protective equipment (PPE) such as gloves and safety goggles.

In conclusion, 1?2?3?4?5?6?7?8-Octahydrophenanthrene (CAS No. 5325-97-3) is a versatile compound with a wide range of applications in chemistry and materials science. Its unique chemical properties make it an essential component in various research and industrial processes. Ongoing research continues to uncover new possibilities for its use in advanced materials and pharmaceuticals.

• 26655-71-0(octahydroanthracene)
• 2809-37-2(Naphthalene, 1,2,3,4-tetrahydro-5,6,8-trimethyl-)
• 20027-77-4(5,6-dimethyl-1,2,3,4-tetrahydronaphthalene)
• 64094-26-4(Naphthalene, 2,2'-(1,4-butanediyl)bis[5,6,7,8-tetrahydro-1,3,4-trimethyl-)
• 27216-28-0(Naphthalene, tetrahydro-)
• 496857-20-6(Naphthalene, 1,2,3,4-tetrahydro-5,8-dipropyl-)
• 119-64-2(1,2,3,4-Tetrahydronaphthalene)
• 1610-39-5(1,2,3,4,5,6,7,8,9,10,11,12-Dodecahydrotriphenylene)
• 243969-88-2(Naphthalene, 1,4-diethyl-5,6,7,8-tetrahydro-2,3-dipropyl-)
• 19063-11-7(Naphthalene, 1,2,3,4-tetrahydro-5,6,7,8-tetramethyl-)