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91935-18-1

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91935-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91935-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,3 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91935-18:
(7*9)+(6*1)+(5*9)+(4*3)+(3*5)+(2*1)+(1*8)=151
151 % 10 = 1
So 91935-18-1 is a valid CAS Registry Number.

91935-18-1Relevant articles and documents

N -Alkyl substituted 1 H -benzimidazoles as improved n-type dopants for a naphthalene-diimide based copolymer

Saglio,Mura,Massetti,Scuratti,Beretta,Jiao,McNeill,Sommer,Famulari,Lanzani,Caironi,Bertarelli

, p. 15294 - 15302 (2018)

Doped polymer semiconductors are actively studied for opto- and micro-electronic applications including thermoelectric generators, where a high electrical conductivity is a key factor. In general, n-type doping is more challenging to achieve than p-type doping. Here we study n-type doping of a commonly used electron transporting naphthalene-diimide bithiophene copolymer with a series of air-stable and solution-processable benzimidazole dopants. To understand the role of dopant structure on miscibility and the resulting conductivity, benzimidazoles with different linear and branched alkyl substituents were synthesized, and their doping efficacy compared through combined morphological, electrical and thermoelectric characterization. We observe a clear dependence of the nature of the alkyl substituent on dopant intercalation into the semicrystalline morphology. By increasing the length or the steric hindrance of the alkyl substituents, the miscibility between dopant and copolymer is enhanced leading to optimized electrical conductivity.

New experiments in the reductive N-alkylation and N-peralkylation of aromatic amines

Verardo,Giumanini,Strazzolini

, p. 609 - 627 (2007/10/02)

Some secondary and primary aromatic amines were variously N-alkylated and N-peralkylated by the aldehyde-sodium borohydride procedure in acidic aqueous solution. The procedure lends itself to the α-mono and α,α1-dideuterium labelling of the new N-substituent(s).

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