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4,5-Bis-(2-chloro-ethylsulfanyl)-[1,3]dithiole-2-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138682-23-2

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138682-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138682-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,8 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 138682-23:
(8*1)+(7*3)+(6*8)+(5*6)+(4*8)+(3*2)+(2*2)+(1*3)=152
152 % 10 = 2
So 138682-23-2 is a valid CAS Registry Number.

138682-23-2SDS

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 4,5-bis(2-chloroethylsulfanyl)-1,3-dithiole-2-thione

1.2 Other means of identification

Product number -
Other names 4,5-BIS(2-CHLORO-ETHYLSULFANYL)-[1,3]DITHIOLE-2-THIONE

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:138682-23-2 SDS

138682-23-2Relevant academic research and scientific papers

Chalcogenation of Tetrathiafulvalene (TTF): Synthesis of Alkylthio-TTF and Alkylseleno-TTF Derivatives and X-Ray Crystal Structure of Ethylenediseleno-TTF (EDS-TTF)

Moore, Adrian J.,Bryce, Martin R.,Cooke, Graeme,Marshallsay, Gary J.,Skabara, Peter J.,et al.

, p. 1403 - 1410 (1993)

The reaction of mono-lithiated tetrathiafulvalene (TTF) with elemental sulfur or elemental selenium at -78 deg C yields the transient species TTF-S(1-) Li(1+) and TTF-Se(1-) Li(1+), respectively, which have been trapped with a range of alkyl halides to yi

Highly-functionalised Tetrathiafulvalene (TTF) Derivatives

Moore, Adrian J.,Bryce, Martin R.

, p. 1638 - 1639 (1991)

Efficient syntheses are described for a range of new functionalised tetrathiafulvalene donors, notably those substituted with vinylthio and acrylate groups; solution redox properties have been studied by cyclic voltammetry.

Syntheses, Unique Strained Molecular Structures, and Unusual Transannular Electronic Interactions of a Series of Crisscross-Overlapped Tetrathiafulvalenophanes

Takimiya, Kazuo,Imamura, Koichi,Shibata, Youji,Aso, Yoshio,Ogura, Fumio,Otsubo, Tetsuo

, p. 5567 - 5574 (2007/10/03)

A series of novel tetrathiafulvalenophanes has been synthesized, in which two tetrathiafulvalenes (TTF) are linked in a crisscross-overlapped arrangement by four alkylenedithio bridges. Their molecular structures were elucidated by X-ray crystal analyses,

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