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155904-20-4

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155904-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155904-20-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,9,0 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 155904-20:
(8*1)+(7*5)+(6*5)+(5*9)+(4*0)+(3*4)+(2*2)+(1*0)=134
134 % 10 = 4
So 155904-20-4 is a valid CAS Registry Number.

155904-20-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Diiodobenzo(1,2-b:4,5-b')dithiophene

1.2 Other means of identification

Product number -
Other names 2,6-diiodobenzo[1,2-b:4,5-b']dithiophene

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:155904-20-4 SDS

155904-20-4Relevant articles and documents

Novel Electron Acceptors Bearing a Heteroquinonoid System. 4. Syntheses, Properties, and Charge-Transfer Complexes of 2,7-Bis(dicyanomethylene)-2,7-dihydrobenzodithiophene, 2,7-Bis(dicyanomethylene)-2,7-dihydrobenzodithiophene, and 2,6-Bis(dicyanomethylene)...

Yoshida, Shu,Fujii, Masanori,Aso, Yoshio,Otsubo, Tetsuo,Ogura, Fumio

, p. 3077 - 3081 (2007/10/02)

The three title compounds were prepared as novel hetero-TCNQ electron acceptors comprising the quinonoid skeletons of different benzodithiophene types between two dicyanomethylene groups.On the basis of cyclic voltammetry, they have electron affinities comparable to or stronger than that of TCNQ.In addition, the extensive building blocks serve to induce the effective reduction of on-site coulombic repulsion.They thus behaved as superior electron acceptors for forming electrically conductive charge-transfer complexes.In particular, 2,7-bis(dicyanomethylene)-2,7-dihydrobenzodithiophene was the most tractable in terms of stability and solubility, giving a variety of conductive complexes with typical electron donors of TTT, TTF, and TPBP types.Most of these complexes showed a characteristic broad electronic transition in the infrared region of 2.9-4.0 kcm-1, supporting the idea that their crystal structures assume a stacking form of segregated donor and acceptor columns with mixed valence states.

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