144970-32-1

Basic information

• Product Name: 1,3,5,7-tetrakis(4-ethinylphenyl)adamantane
• Synonyms: 1,3,5,7-tetrakis(4-ethinylphenyl)adamantane
• CAS NO: 144970-32-1
• Molecular Weight: 536.716
• Mol File: 144970-32-1.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 649.0±55.0 °C(Predicted)
• Density: 1.21±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 1,3,5,7-tetrakis(4-ethinylphenyl)adamantane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5,7-tetrakis(4-ethinylphenyl)adamantane(144970-32-1)
• EPA Substance Registry System: 1,3,5,7-tetrakis(4-ethinylphenyl)adamantane(144970-32-1)

Safety Data

• Hazardous Substances Data: 144970-32-1(Hazardous Substances Data)

Usage

Chemical structure

1,3,5,7-tetrakis(4-ethinylphenyl)adamantane is a compound with an adamantane core surrounded by four 4-ethinylphenyl groups.

Symmetry

The compound has a symmetrical structure, which contributes to its rigidity and potential applications in various fields.

Rigid structure

The rigidity of the compound is due to its adamantane core and the attachment of 4-ethinylphenyl groups, making it suitable for use in materials science and nanotechnology.

Potential applications

The compound has been studied for its potential use in materials science, nanotechnology, and pharmaceutical research.

Building block

It has been investigated as a building block for designing new organic materials with specific properties.

Drug delivery system

The compound has been explored as a potential drug delivery system due to its unique structure and properties.

Chemical and physical studies

The compound's unique structure and properties make it an interesting target for further chemical and physical studies to explore its potential applications and properties.

Upstream product

• 144970-30-9 1,3,5,7-tetrakis(4-iodophenyl)adamantane 
• 768-90-1 1-Adamantyl bromide 
• 71-43-2 benzene 
• 16004-75-4 1,3,5,7-tetrakis(phenyl)adamantane 
• 1066-54-2 trimethylsilylacetylene 

Downstream Products

• 1201839-76-0 tetrakis[4-(1-(N₄-benzoyl-2',3'-dideoxycytidine-3'-yl)-1,2,3-triazol-4-yl)phenyl]adamantane 
• 1287733-18-9 octaethyl 5,5',5'',5'''-[adamantane-1,3,5,7-tetrayltetrakis(4,1-phenyleneethyne-2,1-diyl)]tetraisophthalate 
• 1287733-25-8 1,3,5,7-tetrakis(4-(pyridyl-4′-yl-ethynyl)phenyl)adamantine 
• 1287733-15-6 1,3,5,7-tetrakis{4-[(4-methoxyphenyl)ethynyl]phenyl}adamantane 
• 1287733-17-8 tetraethyl 4,4',4'',4'''-[adamantane-1,3,5,7-tetrayltetrakis(4,1-phenyleneethyne-2,1-diyl)]tetrabenzoate 
• 1287733-23-6 1,3,5,7-tetrakis[4-(3-pyridylethynyl)phenyl]adamantane 
• 1287733-19-0 1,3,5,7-tetrakis[4-(2-pyridylethynyl)phenyl]adamantane 
• 1201839-52-2 1,3,5,7-tetrakis(4-(1-phenyl-1,2,3-triazol-4-yl)phenyl)adamantane 
• 1201839-62-4 (S,S,S,S)-4,4',4'',4'''-(1,3,5,7-adamantanetetrayl)tetra-4-phenyl-1H-1,2,3-triazole-1-acetic acid tetraethyl ester 
• 1201839-74-8 1,3,5,7-tetrakis[4-(1-(3'-deoxythymidin-3'-yl)-1,2,3-triazol-4-yl)phenyl]adamantane 
• 1201839-56-6 1,3,5,7-tetrakis(4-(1-(4-fluorophenyl)-1,2,3-triazol-4-yl)phenyl)adamantane 

Relevant articles and documents

Weak hydrogen bonding between acetylenic groups: The formation of diamondoid nets in the crystal structure of tetrakis(4-ethynylphenyl)methane.

The crystal structure of tetrakis(4-ethynylphenyl)methane 1 shows interwoven diamondoid lattices formed by weak hydrogen bonds between the acetylenic groups, while 1,3,5,7-tetrakis(4-ethynylphenyl)adamantane 2 crystallizes in a non-symmetrical network.

Preparation of a microporous organic polymer by the thiol-yne addition reaction and formation of Au nanoparticles inside the polymer

A microporous polymer with sulfide and thiol groups was synthesized using the thiol-yne reaction. Au nanoparticles were prepared by in situ reduction reaction inside the polymer and were found to be well dispersed. The Au-containing polymer showed catalytic activity in the reduction of 4-nitrophenol.

A modular approach for the synthesis of nanometer-sized polynitroxide multi-spin systems

The synthesis of rigid symmetric polyradical model systems with inter-spin distances between 1.4 and 4 nm and their room temperature continuous wave (CW) EPR spectra are reported. Conditions for attachment of the spin-label via esterification have been op