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9-phenyl-9H-thioxanthen-9-ol 10,10-dioxide, also known as 9-phenyl-9H-thioxanthene-9-ol, 10,10-dioxide, is a chemical compound with the molecular formula C21H13OS2. It is a derivative of the thioxanthene class of compounds, characterized by the presence of a sulfur atom in the central ring structure. This specific compound features a phenyl group attached to the central ring, and a hydroxyl group at the 9-position. The 10,10-dioxide notation indicates the presence of two oxygen atoms bonded to the carbon atoms at the 10-position, forming a dioxide group. 9-phenyl-9H-thioxanthen-9-ol 10,10-dioxide is known for its potential applications in the synthesis of various pharmaceuticals and organic compounds, as well as its use as an intermediate in chemical reactions.

6630-81-5

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6630-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6630-81-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6630-81:
(6*6)+(5*6)+(4*3)+(3*0)+(2*8)+(1*1)=95
95 % 10 = 5
So 6630-81-5 is a valid CAS Registry Number.

6630-81-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 10,10-dioxo-9-phenylthioxanthen-9-ol

1.2 Other means of identification

Product number -
Other names 9-Phenyl-9H-thioxanthen-9-ol 10,10-dioxide

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:6630-81-5 SDS

6630-81-5Downstream Products

6630-81-5Relevant academic research and scientific papers

Friedel-Crafts arylmethylation: A simple approach to synthesize bipolar host materials for efficient electroluminescence

Ou, Chang-Jin,Lin, Jin-Yi,Mao, Jie,Chu, Shuang-Quan,Zhao, Yu,Xie, Ling-Hai,Cao, Hong-Tao,Zhang, Xin-Wen,Wei, Ying,Huang, Wei

, p. 370 - 378 (2016)

In order to simplify the synthesis of bipolar host materials of OLEDs, a facile synthetic approach was developed and a series of sulfone-contained bipolar host materials were synthesized via mild one-step Friedel-Crafts arylmethylation. Due to π-conjugate-interrupted connection between donor moiety and sulfone moiety, those materials keep high triplet energy and separate the HOMO and LUMO levels. Furthermore, the introduction of sulfone group can significantly lower LUMO level. Based on newly synthesized sulfone-based bipolar host materials, efficient solution-processed sky-blue phosphorescent OLEDs were fabricated with high current efficiency of 16.5?cd/A. Our results demonstrate Friedel-Crafts arylmethylation is powerful synthetic strategy to construct bipolar host materials.

Synthesis of o-Substituted Phenols by Criegee Rearrangement of Benzylic Hydroperoxides

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

, p. 931 - 934 (2007/10/02)

9-Phenylthioxanthen-9-ol, 10,10-dimethyl-9-phenyl-9,10-dihydroanthracen-9-ol, and 9-arylfluoren-9-ols undergo Criegee-type rearrangements when treated with hydrogen peroxide and acid to generate substituted benzophenones from the first two substrates, and monoesters of biphenyl-2,2'-diol from the fluorenes via subsequent Bayer-Villiger oxidation of the intermediate 2'-aroylbiphenyl-2-ol. 5-Phenyl-10,11-dihydrodibenzocyclohepten-5-ol and its dehydroderivative gave the corresponding heptanone and heptenone on treatment with acid and hydrogen peroxide.Prolonged reaction of the 5-phenyldibenzohepten-5-ol afforded products arising from oxidation of the double bond.

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