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1,3-diphenyl-8H-indeno[1,2-c]thiophen-8-one is a complex organic compound characterized by a unique molecular structure. It belongs to the family of indeno[1,2-c]thiophenes, which are heterocyclic compounds with a sulfur atom in the ring. This particular compound features two phenyl groups attached to the 1 and 3 positions of the indenothiophene core, which contributes to its stability and electronic properties. The compound is of interest in the field of organic chemistry, potentially for its electronic and optical properties, which could make it a candidate for applications in materials science, such as in the development of organic semiconductors or as a component in electronic devices. Its chemical structure and properties make it a subject of study for researchers exploring new compounds with specific functionalities.

5706-22-9

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5706-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5706-22-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,0 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5706-22:
(6*5)+(5*7)+(4*0)+(3*6)+(2*2)+(1*2)=89
89 % 10 = 9
So 5706-22-9 is a valid CAS Registry Number.

5706-22-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Diphenyl-indeno[1,2-c]thiophen-4-on

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5706-22-9 SDS

5706-22-9Downstream Products

5706-22-9Relevant academic research and scientific papers

Catalytic Sulfur-Enabled Dehydrobicyclization of 1,6-Enynes toward Arylated Indeno[1,2-c]thiophenes

Wu, Ya-Nan,Fu, Rong,Wang, Nan-Nan,Hao, Wen-Juan,Li, Guigen,Tu, Shu-Jiang,Jiang, Bo

, p. 4762 - 4770 (2016/07/06)

A new copper-catalyzed sulfur-enabled dehydrobicyclization of 1,6-enynes using potassium sulfide as a sulfurating reagent has been established, providing a straightforward access toward arylated indeno[1,2-c]thiophenes with moderate to good yields. This sulfur incorporation pathway involves Michael addition, 5-exo-dig/5-endo-trig bicyclization and dehydrogenation sequence, resulting in continuous multiple bond-forming events including C-S and C-C bonds to rapidly construct functional organic molecules.

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