128562
Hexaketocyclohexane octahydrate
97%
Synonym(s):
Cyclohexanehexone octahydrate, Triquinoyl octahydrate
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About This Item
Empirical Formula (Hill Notation):
C6O6 · 8H2O
CAS Number:
Molecular Weight:
312.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
Hexaketocyclohexane octahydrate, 97%
InChI
1S/C6O6.8H2O/c7-1-2(8)4(10)6(12)5(11)3(1)9;;;;;;;;/h;8*1H2
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 key
MQIMWEBORAIJPP-UHFFFAOYSA-N
assay
97%
form
powder
mp
99 °C (dec.) (lit.)
functional group
ketone
storage temp.
2-8°C
Quality Level
Related Categories
Application
Hexaketocyclohexane octahydrate has been used in the preparation of hexaazatriphenylenehexacarbonitrile.
General description
Hexaketocyclohexane octahydrate also known as Triquinoyl octahydrate is an organic compound, often utilized as a building block in various organic reactions, including the synthesis of water-soluble π-conjugated hexaazatrinaphthylenes and their derivatives.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Nitrogen-rich layered carbon for adsorption of typical volatile organic compounds and low-temperature thermal regeneration
Li Tan, et al.
Journal of Hazardous Materials, 424, 127348-127348 (2022)
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)
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
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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