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6,7-Dihydro-1,4-diphenyl-5H-cyclopenta[d]pyridazine is a complex organic chemical compound with the molecular formula C21H19N. It features a cyclopenta[d]pyridazine ring system, which is a fused ring structure consisting of a cyclopentane and a pyridazine. The compound is characterized by two phenyl groups attached to the 1,4-positions of the cyclopenta[d]pyridazine core, and a dihydro functional group, indicating the presence of two hydrogen atoms in a reduced state. 6,7-Dihydro-1,4-diphenyl-5H-cyclopentapyridazine is of interest in medicinal chemistry and may have potential applications in the development of pharmaceuticals due to its unique structure and properties.

2272-61-9

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2272-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2272-61-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,7 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2272-61:
(6*2)+(5*2)+(4*7)+(3*2)+(2*6)+(1*1)=69
69 % 10 = 9
So 2272-61-9 is a valid CAS Registry Number.

2272-61-9Downstream Products

2272-61-9Relevant academic research and scientific papers

Improved and practical procedures for the preparation of highly substituted pyridines and pyridazines via silica-mediated aromatisation

Catozzi, Nicola,Bromley, William J.,Wasnaire, Pierre,Gibson, Mairi,Taylor, Richard J. K.

, p. 2217 - 2221 (2007)

A new and straightforward procedure is described for the preparation of highly substituted pyridines and pyridazines. The method involves a Diels-Alder/retro-Diels-Alder sequence leading to dihydropyridine or related intermediates, which can be aromatized

Proline-catalyzed direct inverse electron demand diels-alder reactions of ketones with 1,2,4,5-tetrazines

Xie, Hexin,Zu, Liansuo,Oueis, Hanine R.,Li, Hao,Wang, Jian,Wang, Wei

supporting information; experimental part, p. 1923 - 1926 (2009/04/08)

An organocatalytic direct inverse electron demand Diels-Alder reaction of ketones with 1,2,4,5-tetrazines has been developed. The process is efficiently catalyzed by proline to give Diels-Alder adducts pyridazines in high yields.

SYNTHESIS OF NOVEL HETEROCYCLIC CLEFTS DERIVED FROM TETRACYCLO4,11.05,9>UNDECANE-3,6-DIONE AND TRICYCLO2,6>UNDECANE-3,11-DIONE

Haddadin, Makhluf J.,Wang, Yanjun,Frenkel, Svetlana,Bott, Simon G.,Yang, Lei,et al.

, p. 869 - 882 (2007/10/02)

New molecular clefts (6a-6c), (9a), and (9b) have been prepared via base promoted reactions of 3,6-diaryl-1,2,4,5-tetrazines with tetracyclo4,11.05,9>undecane-3,6-dione (1) and with tricyclo2,6>undecane-3,1

Diels-Alder Reactions of 3,6-Diphenyl-1,2,4,5-Tetrazine and 3,6-Di(2-pyridyl)-1,2,4,5-tetrazine with some 1-Morpholinocycloalkenes

Atfah, M. Adnan

, p. 717 - 719 (2007/10/02)

The reactions of 3,6-diphenyl-1,2,4,5-tetrazine 1 and 3,6-di(2-pyridyl)-1,2,4,5-tetrazine 2 with the enamines 3a-d derived from morpholine and the 5-,6-,7- and 8-membered cyclic ketones have been investigated.A number of pyridazine derivatives 4-7 most of

Cycloaddition Reactions with Azabenzenes, XIV. - Synthesis of Benzocyclopentisoquinolines and Benzocyclopentisoquinolines (12-Azasteroids)

Neunhoeffer, Hans,Metz, Hans-Joachim

, p. 1476 - 1495 (2007/10/02)

Reaction of methyl cyclopenta-1,2,4-triazine-3-carboxylate (5a) with 1-(6-methoxy-3,4-dihydro-1-naphthyl)pyrrolidine (4a) and with 1-(6-methoxy-3,4-dihydro-2-naphthyl)pyrrolidine (4b) yields the benzocyclopentisoquinolinecarboxylate 6a and the be

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