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1,1,4,4-Tetrakis(4-dimethylaminophenyl)-2,3-diaza-1,3-butadiene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82907-50-4

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82907-50-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82907-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,0 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82907-50:
(7*8)+(6*2)+(5*9)+(4*0)+(3*7)+(2*5)+(1*0)=144
144 % 10 = 4
So 82907-50-4 is a valid CAS Registry Number.

82907-50-4Relevant academic research and scientific papers

Two Amphoteric Silver Carbene Clusters

Tskhovrebov, Alexander G.,Goddard, Richard,Fürstner, Alois

, p. 8089 - 8094 (2018/06/29)

Two highly labile silver carbene cluster complexes are described, which are unique in that they mark the transition point at which the carbene center transmutes from a fairly common NHC-like nucleophilic behavior to an electrophilic character befitting reactive silver carbene intermediates of relevance in various catalytic transformations. This amphoteric character is the distinguishing attribute of a μ-bridged donor/donor carbene entity that connects two silver atoms of triangular or tetrahedral metallic core units.

Tetraethylammonium bromide catalysed phase transfer reaction of potassium superoxide with hydrazones and tosylhydrazones

Kumar,Singh

, p. 579 - 583 (2007/10/03)

A variety of hydrazones and tosylhydrazones of carbonyl compounds have been investigated under the mild reaction conditions of potassium superoxide and tetraethylammonium bromide in dry dimethylformamide. As a result, hydrazones are generally transformed to their corresponding azines whereas tosylhydrazones undergo facile fragmentation to give the olefinic products in fairly good yields. The study highlights the use of tetraethylammonium bromide as an efficient and inexpensive catalyst for superoxide studies.

Multistep Redox Systems, LXVIII. Violene/Cyanine Hybrids as Electrochromics Part 2: Tetrakis(4-dimethylaminophenyl)ethene and Its Derivatives

Huenig, Siegfried,Kemmer, Martina,Wenner, Hermann,Barbosa, Frederique,Gescheidt, Georg,Perepichka, Igor F.,Baeuerle, Peter,Emge, Andreas,Peters, Karl

, p. 2618 - 2632 (2007/10/03)

The general structure of violene/cyanine hybrids (see below) is exemplified by tetrakis(4-dimethylamino phenyl)ethene 1RED its vinylogue 2RED and its diazavinylogue 3RED. As judged from their cyclic voltammograms and spect

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