38614-05-0

Basic information

• Product Name: 1-phenoxytricyclo[3.3.1.1~3,7~]decane
• CAS NO: 38614-05-0
• Molecular Formula: C₁₆H₂₀O
• Molecular Weight: 228.3294
• Mol File: 38614-05-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 326.5°C at 760 mmHg
• Flash Point: 128.6°C
• Density: 1.12g/cm³
• Vapor Pressure: 0.00041mmHg at 25°C
• Refractive Index: 1.586
• CAS DataBase Reference: 1-phenoxytricyclo[3.3.1.1~3,7~]decane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenoxytricyclo[3.3.1.1~3,7~]decane(38614-05-0)
• EPA Substance Registry System: 1-phenoxytricyclo[3.3.1.1~3,7~]decane(38614-05-0)

Safety Data

• Hazardous Substances Data: 38614-05-0(Hazardous Substances Data)

Usage

Tricyclic structure

The compound has a unique structure consisting of three fused rings, which contribute to its stability and potential applications.

Phenoxy group attachment

A phenoxy group is attached to one of the carbon atoms in the tricyclic structure, which may influence its chemical reactivity and properties.

Molar mass

254.37 g/mol The molar mass represents the mass of one mole of the compound, which can be useful in determining its physical and chemical properties.

Bicyclic compound

Although the compound has a tricyclic structure, it is classified as a bicyclic compound due to the presence of two chemically distinct rings.

Potential applications

The compound may have potential uses in various fields such as pharmaceuticals, agrochemicals, and material science, owing to its unique molecular structure and properties.

Need for further research

To fully understand the potential uses and benefits of 1-phenoxytricyclo[3.3.1.1^3,7^]decane, further research and exploration of its properties are necessary.

Upstream product

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• 108-95-2 phenol 
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Relevant articles and documents

Alkylphosphinites as Synthons for Stabilized Carbocations

We present a new acid-free method for the generation of carbocations based on a redox condensation reaction that enables SN1 reactions with a variety of nucleophiles. We utilize readily synthesized phosphinites that are activated by diisopropyl azodicarboxylate to form betaine structures that collapse upon adding a pronucleophile, thereby yielding reactive carbocation intermediates. We also employ this approach for the alkylation of some bioactive molecules.

Copper(II)-catalyzed O-phenylation of alcohols with organobismuth(V) reagents: A convenient method for the synthesis of simple tert-alkyl phenyl ethers

A convenient method for copper(II)-catalyzed O-phenylation of simple alcohols with organobismuth(V) compounds under mild conditions is described. Treatment of tetraphenylbismuth fluoride (Ph4BiF) with various simple alcohols in the presence of

REACTION OF PHENOL WITH 1-HYDROXYADAMANTANE IN THE PRESENCE OF ALUMINUM DIPHENYL DITHIOPHOSPHATE

The reaction of phenol with 1-hydroxyadamantane in the presence of aluminum diphenyl dithiophosphate leads to a mixture of mono-, di-, and tri(1-adamantyl)phenols and 1-adamantyl phenyl ether.As a rule the 2-(1-adamantyl)phenol predominates in the mixture.