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Hexaketocyclohexane octahydrate

Name: Hexaketocyclohexane octahydrate
Brand: ALDRICH

97%

Synonym(s):

Cyclohexanehexone octahydrate, Triquinoyl octahydrate

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About This Item

Empirical Formula (Hill Notation):

C₆O₆ · 8H₂O

CAS Number:

527-31-1

Molecular Weight:

312.18

MDL number:

MFCD00149074

UNSPSC Code:

12352100

PubChem Substance ID:

24847867

NACRES:

NA.22

Quality Level

100

Assay

97%

form

powder

mp

99 °C (dec.) (lit.)

storage temp.

2-8°C

SMILES string

[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].O=C1C(=O)C(=O)C(=O)C(=O)C1=O

InChI

1S/C6O6.8H2O/c7-1-2(8)4(10)6(12)5(11)3(1)9;;;;;;;;/h;8*1H2

InChI key

MQIMWEBORAIJPP-UHFFFAOYSA-N

Related Categories

Organic Building Blocks

Application

Hexaketocyclohexane octahydrate has been used in the preparation of hexaazatriphenylenehexacarbonitrile.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Synthesis and some reactions of hexaazatriphenylenehexanitrile, a hydrogen-free polyfunctional heterocycle with D3h symmetry.

Kanakarajan K and Czarnik AW.

The Journal of Organic Chemistry, 51(26), 5241-5243 (1986)

Photocatalytic oxygen evolution from low-bandgap conjugated microporous polymer nanosheets: a combined first-principles calculation and experimental study.

Lei Wang et al.

Nanoscale, 9(12), 4090-4096 (2017-03-16)

Nanostructured semiconducting polymers have emerged as a very promising class of metal-free photocatalytic materials for solar water splitting. However, they generally exhibit low efficiency and lack the ability to utilize long-wavelength photons in a photocatalytic oxygen evolution reaction (OER). Here

Conductive Metal-Organic Frameworks with Extra Metallic Sites as an Efficient Electrocatalyst for the Hydrogen Evolution Reaction.

Hao Huang et al.

Advanced science (Weinheim, Baden-Wurttemberg, Germany), 7(9), 2000012-2000012 (2020-05-10)

The 2D conductive metal-organic frameworks (MOFs) are expected to be an ideal electrocatalyst due to their high utilization of metal atoms. Exploring a new conjugated ligand with extra active metallic center can further boost the structural advantages of conductive MOFs.

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