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(E)-3-<2-(4-methoxyphenyl)ethenyl>pyridazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83539-85-9

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83539-85-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83539-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,3 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83539-85:
(7*8)+(6*3)+(5*5)+(4*3)+(3*9)+(2*8)+(1*5)=159
159 % 10 = 9
So 83539-85-9 is a valid CAS Registry Number.

83539-85-9Downstream Products

83539-85-9Relevant academic research and scientific papers

New pyrrolopyridazine derivatives as blue organic luminophors

Swamy,Min, Sun Park,Su, Jung Han,Sook, Kyung Kim,Ju, Hee Kim,Lee, Chongmok,Bang, Hyunjin,Kim, Youngmee,Kim, Sung-Jin,Yoon, Juyoung

, p. 10227 - 10234 (2005)

New pyrrolopyridazine derivatives were synthesized as potential blue organic luminophors. Three different classes of pyrrolopyridazine derivatives were made, for example, aryl groups directly connected to the core PPY (pyrrolo[1,2-b]pyridazine-5,6,7-tricarboxylic acid trimethyl ester) moiety, aryl groups connected to the PPY via a vinylene linker and aryl groups connected to the PPY via an acetylene linker. Their optical and electrochemical properties were productively compared. One of the derivatives 2 showed a relative quantum yield as high as 0.9. Compound 8 in the vinyl bridged pyrrolopyridazine series has been characterized by its X-ray crystal structure analysis.

Ruthenium(II)-Catalyzed C-H (Hetero)Arylation of Alkenylic 1,n-Diazines (n = 2, 3, and 4): Scope, Mechanism, and Application in Tandem Hydrogenations

Gramage-Doria, Rafael,Achelle, Sylvain,Bruneau, Christian,Robin-Le Guen, Fran?oise,Dorcet, Vincent,Roisnel, Thierry

, p. 1462 - 1477 (2018/02/09)

A general ruthenium(II)-catalyzed methodology enabling the (hetero)arylation of alkenylic C-H bonds utilizing a series of synthetically appealing diazines as directing groups is presented. Despite the presence of additional nitrogen lone pairs remote from

Quaternary ammonium salt-assisted synthesis of extended π-systems from methyldiazines and aromatic aldehydes

Vanden Eynde,Pascal,Van Haverbeke,Dubois

, p. 3167 - 3173 (2007/10/03)

4-Methyl- and 4,6-dimethylpyrimidines, methyl- and 2,5-dimethylpyrazines, as well as 3-methylpyridazine readily react with aromatic aldehydes in a hot solution of sodium hydroxide in the presence of a catalytic amount of a quaternary ammonium salt and in

4'-Hydroxystyryldiazines: Synthesis and fluorescence properties

Haroutounian,Katzenellenbogen

, p. 1585 - 1598 (2007/10/02)

In order to investigate the effect that additional nitrogen substitution in the 4'-hydroxystyrylpyridine system would have on the photophysical properties of this molecule, we have synthesized a series of four isomeric 4'-hydroxystyryldiazines: the 2,4-di

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