75534-58-6

Basic information

• Product Name: 1,3,5,7-tetrakis(hydroxymethyl)adamantane
• CAS NO: 75534-58-6
• Molecular Weight: 256.342
• Mol File: 75534-58-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,3,5,7-tetrakis(hydroxymethyl)adamantane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5,7-tetrakis(hydroxymethyl)adamantane(75534-58-6)
• EPA Substance Registry System: 1,3,5,7-tetrakis(hydroxymethyl)adamantane(75534-58-6)

Safety Data

• Hazardous Substances Data: 75534-58-6(Hazardous Substances Data)

Usage

Class

Adamantane derivatives

Structure

Cage-like molecule with four hydroxymethyl groups attached to carbon atoms at positions 1, 3, 5, and 7

Thermal stability

High

Applications

a. Building block for functionalized nanostructured materials
b. Polymer composites
c. Nanocomposites
d. Advanced ceramics
e. Drug delivery
f. Catalysis
g. Surface modification

Potential uses

Energy storage (enhancing performance of lithium-ion batteries and fuel cells)

Upstream product

• 101892-34-6 1,3,5,7-tetracarboxymethyladamantane 
• 29713-15-3 1,3-adamantanedicarbonyl chloride 
• 39269-10-8 adamantane-1,3-dicarboxylic acid 
• 101892-34-6 tetramethyl adamantane-1,3,5,7-tetracarboxylate 
• 100884-80-8 adamantane-1,3,5,7-tetracarboxylic acid 
• 16004-75-4 1,3,5,7-tetrakis(phenyl)adamantane 
• 768-90-1 1-Adamantyl bromide 
• 100884-80-8 adamantane-1,3,5,7-tetracarboxylic acid 

Downstream Products

• 1687-36-1 1,3,5,7-tetramethyl-adamantane 
• 84782-74-1 adamantane-1,3,5,7-tetramethanol tetratosylate 

Relevant articles and documents

Four-Directional synthesis of adamantane derivatives

1-Adamantanemethanol, 1,3-adamantanedimethanol and 1,3,5,7-adamantanetetramethanol were converted into adamantanes functionalized with one or four (2R,1S)-2-formyl-1-cyclopropyl residues using Charette enantioselective cyclopropanation reactions and with one, two or four 4-ethoxy- (or 4-t-butoxy)-3-diazo-2,4- dioxobutyl residues from aldehyde and diazo-acetate ester condensation reactions by 1-directional, 2- directional or 4-directional syntheses. The synthesis of adamantane fused to cyclopentadiene is also reported. 'Equation Presented'.

Chromophore Multiplication To Enable Exciton Delocalization and Triplet Diffusion Following Singlet Fission in Tetrameric Pentacene

A tetrameric pentacene, PT, has been used to explore the effects of exciton delocalization on singlet fission (SF). For the first time, triplet decorrelation through intramolecular triplet diffusion was observed following SF. Transient absorption spectros