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"9H-Xanthene, 9,9'-dioxybis[9-phenyl-" is a complex organic compound with the chemical formula C26H18O2. It is a derivative of xanthene, a tricyclic aromatic hydrocarbon, and features two phenyl groups attached to the xanthene core through a dioxy bridge. 9H-Xanthene, 9,9'-dioxybis[9-phenyl- is known for its potential applications in the synthesis of various dyes, pigments, and pharmaceuticals due to its unique structure and properties. The presence of the dioxy bridge and phenyl groups contributes to its stability and reactivity, making it a valuable intermediate in organic chemistry.

89192-73-4

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89192-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89192-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,9 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89192-73:
(7*8)+(6*9)+(5*1)+(4*9)+(3*2)+(2*7)+(1*3)=174
174 % 10 = 4
So 89192-73-4 is a valid CAS Registry Number.

89192-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-phenyl-9-(9-phenylxanthen-9-yl)peroxyxanthene

1.2 Other means of identification

Product number -
Other names 9-Phenylxanthyl-peroxid

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:89192-73-4 SDS

89192-73-4Relevant academic research and scientific papers

Thermal and Photochemical Decomposition of 9-Arylxanthen-9-yl Hydroperoxides and Peroxides

Goosen, Andre,McCleland, Cedric W.,Taljaard, Benjamin

, p. 995 - 1000 (2007/10/02)

The thermolysis and photolysis of a series of 9-arylxanthenyl hydroperoxides and peroxides have been investigated by means of differential scanning calorimetry, electron paramagnetic spectroscopy and product studies.These relatively stable peroxidic compounds were found to rearrange smoothly on being heated at temperatures > 120 deg C and on photolysis, respectively, through concerted reaction pathways.Photolysis of 9-hydroperoxy-9-phenylxanthene and di(9-phenylxanthen-9-yl)peroxide, respectively, have been shown by EPR spectroscopy to generate 9-phenylxanthenyl radicals which dimerise at low temperatures and reform the free radicals at ambient temperature.

The Mechanism of Benzophenone-sensitised Oxidation of 9-Phenilxanthene with Oxygen

Glover, Stephen A.,Goosen, Andre,McCleland, Cedric W.,Taljaard, Benjamin,Vogel, F. Ruric

, p. 1205 - 1210 (2007/10/02)

From an investigation of the effect of inhibitors, quenchers, and the failure of a singlet sensitiser to effect the oxidation, it is proposed that the benzophenone-sensitised oxidation of 9-phenylxanthene with oxygen is a type I process.Further support for this conclusion is afforded by spectroscopic considerations.Evidence is also presented that the oxidation is a non-chain process, and the effect of acid on the product distribution is discussed.

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