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(4-Butyl-phenyl)-[2,5-dibromo-4-(4-butyl-benzoyl)-thiophen-3-yl]-methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

197370-02-8

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197370-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 197370-02-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,3,7 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 197370-02:
(8*1)+(7*9)+(6*7)+(5*3)+(4*7)+(3*0)+(2*0)+(1*2)=158
158 % 10 = 8
So 197370-02-8 is a valid CAS Registry Number.

197370-02-8Downstream Products

197370-02-8Relevant academic research and scientific papers

Imine-bridged planar poly(phenylenethiophene)s and polythiophenes

Zhang, Qing T.,Tour, James M.

, p. 9624 - 9631 (1997)

Synthetic routes to soluble planar poly(phenylenethiophene)s and polythiophenes are described. The main polymer backbones are synthesized via Pd(0)-catalyzed couplings of the electron-rich N,N'-(bis-tert-butoxycarbonyl)-3,4-diamino-2,5-bis(tri-n- butylsta

Alternating donor/acceptor repeat units in polythiophenes. Intramolecular charge transfer for reducing band gaps in fully substituted conjugated polymers

Zhang, Qing T.,Tour, James M.

, p. 5355 - 5360 (2007/10/03)

This paper describes a method to limit the band gap widening that occurs in fully substituted conjugated polymers. This is done by constructing step growth [AB] polymers where the A-units are electron rich and the B-units are electron deficient. The thiophene-based polymers were prepared by modified Stille polymerizations using Pd(0)/CuI catalyst systems in which aryldibromides were coupled with aryldistannanes. The donor units were N,N′-(bis-tert-butoxycarbonyl)-3,4-diaminothiophene, N,N′-(bis-tert-butoxycarbonyl)-N,N′-(dimethyl)-3,4-diaminothiophene, 3,4-diaminothiophene, or 3,4-dialkoxythiophenes while the acceptor units were 3,4-dinitrothiophene, 3,4-(N-n-butylimido)thiophene, or 3,4-diketone-containing thiophenes. The optical spectra showed λmax values ranging from 400 to 676 nm (solution) and 400-768 (film) for these fully substituted polythiophenes, consistent with significant decreases in the band gaps. Intramolecular charge transfer character between the consecutive units explained the lowering of the band gaps. Two polymer systems based solely on electron deficient thiophenes were prepared via an Ullmann coupling which had optical absorption maxima that were in the range of 300-340 nm; considerably smaller than the λmax values for the donor/acceptor systems. Several model trimers were prepared which had significantly shorter wavelength optical absorptions than their corresponding polymers, thus confirming the need for the extended polymeric backbones.

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