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9-(9-hydroxyxanthen-9-yl)xanthen-9-ol, also known as rubrene, is a chemical compound belonging to the xanthene family. It is a yellow crystalline solid with a molecular formula of C34H22O2 and a molecular weight of 462.53 g/mol. Rubrene is characterized by its unique structure, featuring two xanthene rings connected through a hydroxyl group. 9-(9-hydroxyxanthen-9-yl)xanthen-9-ol exhibits strong fluorescence and is widely used in organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and other optoelectronic applications due to its high charge-carrier mobility and excellent stability. Additionally, rubrene has been studied for its potential use in solar cells and as a photosensitizer in photodynamic therapy. Its chemical properties and applications make it an important compound in the field of organic electronics and materials science.

6272-59-9

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6272-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6272-59-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6272-59:
(6*6)+(5*2)+(4*7)+(3*2)+(2*5)+(1*9)=99
99 % 10 = 9
So 6272-59-9 is a valid CAS Registry Number.

6272-59-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(9-hydroxyxanthen-9-yl)xanthen-9-ol

1.2 Other means of identification

Product number -
Other names Xanthopinacol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6272-59-9 SDS

6272-59-9Relevant academic research and scientific papers

Reduction electrochimique de cetones aromatiques encombrees en milieu aprotique et en presence de chlorure de manganese

Fournier, Francoise,Berthelot, Jacques,Pascal, Yves-Louis

, p. 2121 - 2125 (2007/10/02)

The electrochemical reduction of hindered aromatic ketones which are difficult to reduce can be achieved in an aprotic medium (DMF) on a mercury pool cathode, in presence of Mn(II) chloride, at the reduction potential of the Mn(II)?Mn(0) system, but less negative than that of the ketone itself.There is selective hydrodimerization into an α-glycol, with total lack of polymerization.With dissymetric ketones, the dl diastereomers of the diols are produced preferentially.The effect of manganese is due either to the reduction of a Mn(I) or Mn(0) - ketone complex or to the reduction of the ketone by a film of colloidal manganese on the electrode surface.

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