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Methanone, 2-dibenzothienylphenyl-, also known as 2-(2,3-dihydro-1,4-benzothien-2-yl)phenyl-2-oxoethanone, is an organic compound with the chemical formula C17H12O2S2. It is a derivative of ketone, characterized by the presence of a carbonyl group (C=O) bonded to two carbon atoms. The molecule features a phenyl ring (C6H5) connected to a dibenzothienyl group, which consists of two benzene rings fused to a thiophene ring (a five-membered ring with one sulfur atom). Methanone, 2-dibenzothienylphenyl- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of dyes and pigments. Due to its complex structure, Methanone, 2-dibenzothienylphenyl- is a subject of interest in organic chemistry research, particularly in the development of new synthetic methods and the study of its physical and chemical properties.

6407-30-3

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6407-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6407-30-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,0 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6407-30:
(6*6)+(5*4)+(4*0)+(3*7)+(2*3)+(1*0)=83
83 % 10 = 3
So 6407-30-3 is a valid CAS Registry Number.

6407-30-3SDS

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 dibenzothiophen-2-yl(phenyl)methanone

1.2 Other means of identification

Product number -
Other names Methanone,2-dibenzothienylphenyl

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:6407-30-3 SDS

6407-30-3Downstream Products

6407-30-3Relevant academic research and scientific papers

Thiolate-Initiated Synthesis of Dibenzothiophenes from 2,2′-Bis(methylthio)-1,1′-Biaryl Derivatives through Cleavage of Two Carbon-Sulfur Bonds

Chatani, Naoto,Kawashima, Yuki,Kodama, Takuya,Masuya, Yoshihiro,Tobisu, Mamoru

, p. 1995 - 1999 (2019/10/22)

A catalytic reaction involving the cleavage of two carbon-sulfur bonds in 2,2′-bis(methylthio)-1,1′-biaryl derivatives is reported. This reaction does not require a transition-metal catalyst and is promoted by a thiolate anion. Notably, based on DFT calculations, the product-forming cyclization step is shown to proceed through a concerted nucleophilic aromatic substitution (CS N Ar) mechanism.

Composition and synthesis of aggregation-induced emission materials

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Page/Page column 39-40, (2018/04/20)

The present subject matter relates to compositions containing and synthesis of fluorescent materials e made from tetraphenylethylene (TPE) derivative compounds exhibiting aggregation induced emission (AIE) properties. Further contemplated herein are applications for TPE derivative compounds such as electroluminescent devices since they have a high efficiency, low turn on voltage, and excellent brightness. Additionally, application of TPE derivatives exhibiting AIE properties in various fields such as OLEDs, fingerprinting and forensic technology, and various other biological and industrial sectors are discussed.

Synthesis, aggregation-induced emission, and electroluminescence of dibenzothiophene- and dibenzofuran-containing tetraarylethenes

Xie, Ni,Liu, Yang,Hu, Rongrong,Leung, Nelson L. C.,Arseneault, Mathieu,Tang, Ben Zhong

, p. 958 - 966 (2014/08/18)

Dibenzothiophene- and dibenzofuran-functionalized ethanes were synthesized by the McMurry coupling reaction. The luminogens are faintly emissive when molecularly dissolved in good solvents, but emit intensively when aggregated as nanoparticles in poor sol

NOVEL AROMATIC SULFONIUM SALT COMPOUND, PHOTO-ACID GENERATOR COMPRISING THE SAME AND PHOTOPOLYMERIZABLE COMPOSITION CONTAINING THE SAME, RESIN COMPOSITION FOR OPTICAL THREE-DIMENSIONAL SHAPING, AND METHOD OF OPTICALLY FORMING THREE-DIMENSIONAL SHAPE

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Page/Page column 16-17, (2008/06/13)

Novel aromatic sulfonium salt compounds of general formula (I), photo-acid generators comprising the same, and photo-polymerizable compositions containing the same, capable of providing stereolithographic resin compositions which do not suffer from the hi

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