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Phenol, 2-(1,4-diphenyl-1H-pyrazol-5-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65190-70-7

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65190-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65190-70-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,9 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65190-70:
(7*6)+(6*5)+(5*1)+(4*9)+(3*0)+(2*7)+(1*0)=127
127 % 10 = 7
So 65190-70-7 is a valid CAS Registry Number.

65190-70-7Downstream Products

65190-70-7Relevant academic research and scientific papers

A novel palladium intramolecular diaryl ether formation

Olivera, Roberto,Sanmartin, Raul,Domínguez, Esther

, p. 4357 - 4360 (2000)

This paper presents an efficient methodology for the preparation of dibenzoxepino[4,5-d]pyrazoles using a novel intramolecular palladium catalyzed diaryl ether formation. The effect of different chelating ligand systems, along with the unusual coupling reaction of phenoxides with aryl iodides and non-activated aryl moieties are also reported. (C) 2000 Elsevier Science Ltd.

Revisiting the Ullmann-ether reaction: A concise and amenable synthesis of novel dibenzoxepino[4,5-d]pyrazoles by intramolecular etheration of 4,5-(o,o′-halohydroxy)arylpyrazoles

Olivera, Roberto,SanMartin, Raul,Churruca, Fatima,Dominguez, Esther

, p. 7215 - 7225 (2007/10/03)

A concise synthesis of a series of novel dibenzoxepino[4,5-d]pyrazoles was accomplished by implementation of an intramolecular Ullmann-ether reaction on o,o'-halohydroxy-4,5-diarylpyrazoles mediated by CuBr·DMS. An alternative useful approach based on the palladium-catalyzed biarylether linkage formation (Buchwald-Hartwig reaction) was also successfully applied, offering limitations with regard to the steric demand of the substituents. The synthesis of the key o,o′-halohydroxy-4,5-diarylpyrazole intermediates proceeds through the construction of the heterocyclic ring by a tandem amine-exchange/heterocyclization sequence of 3-N,N-(dimethylamino)-1,2-diarylpropenones with phenylhydrazine followed by basic hydrolysis for deprotection. The enamino ketone precursors were conveniently prepared from the corresponding O-sulfonyloxy and O-benzoyloxy ortho-substituted 1,2-diarylethanones, starting from inexpensive salicylaldehyde or phenylacetic derivatives. Preliminary binding affinity experiments against peripheral and central nervous system receptors have been done with negative results.

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