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Product Code B4221-1g
Price $45

A Fully Conjugated Triphenylene Ligand

As a disc-shaped planar molecule applied in liquid crystals, batteries, and macromolecules


Overview | Product Information | MSDS | Related Products


2,3,6,7,10,11-Hexamethoxytriphenylene (CAS number 808-57-1) is a D3h symmetric molecule functionalized with six methoxy groups at the ortho-positions. 2,3,6,7,10,11-Hexamethoxytriphenylene exhibits high reversibility in electrochemical redox reactions, enabling its application as a cathode material. The battery cell incorporating 40 wt% of 2,3,6,7,10,11-hexamethoxytriphenylene demonstrates full specific capacity at current densities up to 3 C. Being a planar molecule, 2,3,6,7,10,11-Hexamethoxytriphenylene finds its application in fundamental studies on charge-transfer interaction by scanning tunneling microscopy.

2,3,6,7,10,11-Hexamethoxytriphenylene can undergo demethylation with a strong Lewis acid for the synthesis of hexahydroxytriphenylene. Hexahydroxytriphenylene is used to prepare hydrogen-bonded frameworks, supported by its strong ππ interactions.

Triphenylene building block

Triphenylene Building Block

Used in batteries, liquid crystals and porous organic frameworks

Conjugated molecule

Conjugated Molecule

With a planar disc shape

High purity

High Purity

>98% pure

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General Information


CAS Number 808-57-1
Chemical Formula C24H24O6
Full Name 2,3,6,7,10,11-Hexamethoxytriphenylene
Molecular Weight 408.44 g/mol
Synonyms HMTP, HAT
Classification or Family Porous organic frameworks, COFs, Batteries, Liquid crystals, Triphenylenes

Chemical Structure


2,3,6,7,10,11-Hexamethoxytriphenylene chemical structure, CAS 808-57-1
2,3,6,7,10,11-Hexamethoxytriphenylene chemical structure, CAS 808-57-1

Product Details


Purity > 98%
Melting Point N/A
Appearance Brown powder

MSDS Documentation


2,3,6,7,10,11-Hexamethoxytriphenylene MSDS Sheet2,3,6,7,10,11-Hexamethoxytriphenylene MSDS Sheet

References


  • 2,3,6,7,10,11-Hexahydroxytriphenylene tetrahydrate: a new form of an important starting material for supramolecular chemistry and covalent organic frameworks, F. Thébault et al., Acta Cryst. C67, 143–145 (2011); DOI: 10.1107/S0108270111002988.
  • Rational synthesis of bis(hexyloxy)-tetra(hydroxy)-triphenylenes and their derivatives, M. Smith et al., RSC Adv., 4, 38281–38292 (2014); DOI: 10.1039/C4RA06503D.
  • Self-assembly of a triphenylene-based-electron donor molecule on graphene: structural and electronic properties, J. Phys. Chem. C, 126, 9855–9861 (2022).


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