triphenylene-2,3,6,7,10,11-hexol

triphenylene-2,3,6,7,10,11-hexol - Names and Identifiers

Name	2,3,6,7,10,11-HEXAHYDROXYTRIPHENYLENE
Synonyms	Hexahydroxytriphenylene 2,3,6,7,10,11-Triphenylenehexol triphenylene-2,3,6,7,10,11-hexol Triphenylene-2,3,6,7,10,11-hexaol 2,3,6,7,10,11-HEXAHYDROXYTRIPHENYLENE 2,3,6,7,10,11-Hexahydroxytriphenylene Hydrate 2,3,6,7,10,11-HEXAHYDROXYTRIPHENYLENE HYDRATE
CAS	4877-80-9

triphenylene-2,3,6,7,10,11-hexol - Physico-chemical Properties

Molecular Formula	C18H12O6
Molar Mass	324.28
Density	1.778
Melting Point	>300℃
Boling Point	776.3±55.0 °C(Predicted)
pKa	8.46±0.30(Predicted)
Storage Condition	Inert atmosphere,Room Temperature
MDL	MFCD01321170
Use	It is used to manufacture a wide-viewing angle film for a liquid crystal display to improve the viewing angle of the liquid crystal display.

triphenylene-2,3,6,7,10,11-hexol - Risk and Safety

Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
HS Code	29072990

triphenylene-2,3,6,7,10,11-hexol - Upstream Downstream Industry

Raw Materials

2,3,6,7,10,11-HEXAMETHOXYTRIPHENYLENE
1,2-Dimethoxybenzene

triphenylene-2,3,6,7,10,11-hexol - Uses and synthesis methods

application

2,3,6,7,10, 11-hexahydroxytriphenyl can be used to prepare metal organic frameworks (MOFs). Metal organic framework is a kind of material formed by coordination of metal ions and organic ligands. Compared with traditional inorganic porous materials, MOF has higher porosity, larger specific surface area, adjustable pore structure and excellent structural stability, and is widely used in the field of chemical energy storage.

Preparation method

Use ultrasound to react catechol (20g,0.182mol) and hexahydrate/ferric chloride (III)(196.8g,0.728mol) for 24 hours. After the reaction is complete, the mixture is washed with dilute hydrochloric acid and water and extracted with heated cyclopentanone to obtain 2,3,6,7,10, 11-hexahydroxytriphenyl.

Last Update：2024-04-09 21:54:55