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1,3-Dithiole, 4-phenyl-2-(4-phenyl-1,3-dithiol-2-ylidene)-, (2Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100760-33-6

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100760-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100760-33-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,7,6 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100760-33:
(8*1)+(7*0)+(6*0)+(5*7)+(4*6)+(3*0)+(2*3)+(1*3)=76
76 % 10 = 6
So 100760-33-6 is a valid CAS Registry Number.

100760-33-6SDS

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-phenyl-2-(4-phenyl-1,3-dithiol-2-ylidene)-1,3-dithiole

1.2 Other means of identification

Product number -
Other names 1,3-Dithiole,4-phenyl-2-(4-phenyl-1,3-dithiol-2-ylidene)-,(2E)

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:100760-33-6 SDS

100760-33-6Downstream Products

100760-33-6Relevant academic research and scientific papers

Synthesis and electrochemical studies of tetrathiafulvalene derivatives (TTF's) as redox active ligands

Sarhan, Abd El-Wareth A. O.,Murakami, Makoto,Izumi, Taeko

, p. 691 - 694 (2007/10/03)

A simple route for synthesis of new tetrathiafulvalene dimethyl ester (TTF-DME) is reported. The tetrathifulvalene dimethylester (TTF-DME) has been prepared by introducing an ester coordination function as a bifunctional new donor. The redox behavior of t

CLEAVAGE OF 2-METHOXY-1,3-DITHIOLES BY ACIDS

Buza, Daniela,Gradowska, Wanda

, p. 775 - 782 (2007/10/02)

The reaction of 2-methoxy-1,3-dithioles (1) with acids, yielding 1,3-dithiolium salts (2) or 2,2'-bi(1,3-dithiolylidenes) (3) or both, was studied.It was found that the direction of this reaction was determined by the strength and the proportion of the ac

INSERTION OF 1,3-DITHIOLIUM CARBENES INTO N-H BOND OF AMIDES AND IMIDES

Buza, Daniela,Gradowska, Wanda

, p. 1059 - 1069 (2007/10/02)

It was found that 1,3-dithiolium carbenes (4a-d) generated from 2-methoxy-1,3-dithioles (1a-d) were inserted into N-H bond of N-methylbenzamide, acetanilide and succinimide to form N-(1,3-dithiol-2-yl)amides (imides) 8-10, respectively.It was shown that N

Tetrathiafulvalenes. XXI Syntheses of Tetrathiafulvalenes from 2-Alkylthio-, 2-Arylthio- and 2-Alkylseleno-1,3-dithiolium Salts

Fanghaenel, E.,Richter, A. M.,Schukat, G.

, p. 479 - 484 (2007/10/02)

In the reaction of 2-alkylthio-, 2-arylthio- or 2-alkylseleno-1,3-dithiolium salts with trivalent phosphorus compounds in acetonitril tetrathiafulvalenes 2 are formed.As an intermediate we suppose a phosphorane, which reacts with further 1,3-dithiolium sa

REACTIONS OF 1,3-DITHIOLIUM CARBENES IN SITU WITH AROMATIC ALDEHYDES

Buza, Daniela,Gradowska, Wanda

, p. 717 - 729 (2007/10/02)

It was found that 1,3-dithiolium carbenes (3) generated from various 1,3-dithiole derivatives reacted with aromatic aldehydes to form 2-benzoyl-2,2'-(1',3'-dithiolyl)-1,3-dithioles (6).The proposed mechanism of reaction has been discussed.

Organic Metals: a New Synthetic Route to Tetrathiafulvalenes

Coustumer, Gerard Le,Mollier, Yves

, p. 38 - 39 (2007/10/02)

We report here a new synthetic route to tetrathiafulvalenes in asimple one-step synthesis from 2-thioxo-1,3-dithioles.

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