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4,4',5,5',6,6',7,7'-OCTAHYDRODIBENZOTETRATHIAFULVALENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35079-58-4

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35079-58-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35079-58-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,7 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35079-58:
(7*3)+(6*5)+(5*0)+(4*7)+(3*9)+(2*5)+(1*8)=124
124 % 10 = 4
So 35079-58-4 is a valid CAS Registry Number.

35079-58-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4,5,6,7-tetrahydro-1,3-benzodithiol-2-ylidene)-4,5,6,7-tetrahydro-1,3-benzodithiole

1.2 Other means of identification

Product number -
Other names 4,4'5,5',6,6',7,7'-octahydrodibenzotetrathiafulvalene

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:35079-58-4 SDS

35079-58-4Relevant academic research and scientific papers

Synthesis of unsimmetrically substituted tetrathiafulvalenes by the "ylid route". Investigations of selectivity.

Fabre, J. M.,Giral, L.,Gouasmia, A.,Cristau, H. J.,Ribeill, Y.

, p. 823 - 826 (2007/10/02)

The selective synthesis of unsimmetrically substituted tetrathiafulvalenes 1 (R R') using phosphonium ylids 2 and dithiolium salts 3 in THF at -80 deg C has been investigated.Several unsymmetrical tetrathiafulvalenes were obtained in good yield. R,R'=CH3; (CH2)4; o-C6H4.It was also shown that the instability of the phosphonium ylid 2 and dithiolylium 3 under the rreaction conditions leads to the formation of variable amounts of symmetrical terathiafulvalenes 1 (R = R').Therefore, purification of the mixture by column chromatography with CS2 as eluent was necessary.

NEW CONDUCTING SALTS CONTAINING UNSYMMETRICAL ?-DONORS

Giral, L.,Fabre, J. M.,Gouasmia, A.

, p. 4315 - 4318 (2007/10/02)

This communication describes the synthesis and the electrochemical properties of a new type of donor containing sulfur or selenium atoms: the dimethyltetramethylenetetraselenafulvalene 1 and the dimethyltetramethylenetetrathiafulvalene 2.The electrical conductivity of their charge transfer complexes and of some of their radical cation salts are reported.

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

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