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2,2'-Bis(methylthio)-1,1'-biphenyl is an organic compound with the chemical formula C14H14S2. It is a colorless to pale yellow crystalline solid that is insoluble in water but soluble in organic solvents. 2,2'-bis(methylthio)-1,1'-biphenyl is characterized by its biphenyl core, with two methylthio groups attached to the 2 and 2' positions. It is used as a chemical intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. Due to its potential applications and chemical properties, 2,2'-bis(methylthio)-1,1'-biphenyl is a subject of interest in the field of organic chemistry.

7343-32-0

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7343-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7343-32-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,4 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7343-32:
(6*7)+(5*3)+(4*4)+(3*3)+(2*3)+(1*2)=90
90 % 10 = 0
So 7343-32-0 is a valid CAS Registry Number.

7343-32-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2'-bis(methylthio)biphenyl

1.2 Other means of identification

Product number -
Other names 2,2'-Di-(methylthio)-biphenyl

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:7343-32-0 SDS

7343-32-0Downstream Products

7343-32-0Relevant academic research and scientific papers

Synthesis of sulfur-containing aryl and heteroaryl vinyls via Suzuki-Miyaura cross-coupling for the preparation of SERS-active polymers

Perez-Pineiro, Rolando,Dai, Sheng,Alvarez-Puebla, Ramon,Wigginton, James,Al-Hourani, Baker Jawabrah,Fenniri, Hicham

supporting information; experimental part, p. 5467 - 5469 (2010/01/11)

The preparation of sulfur-containing aryl and heteroaryl vinyl co-monomers via Suzuki-Miyaura cross-coupling between the corresponding mercaptomethyl arylboronates and in situ-generated vinyl bromides is described. Surface-enhanced Raman scattering (SERS) studies of the target compounds on gold nanoparticles confirmed their potential as spectroscopic tags in the fabrication of SERS-encoded polymers for combinatorial screening and biomedical diagnostics.

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