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3-Phenyl-[1,2,4]triazolo[3,4-a]isoquinoline is a complex organic compound with the molecular formula C18H12N3. It is a heterocyclic molecule, featuring a triazole ring fused to an isoquinoline ring, with a phenyl group attached to the triazole. 3-phenyl-[1,2,4]triazolo[3,4-a]isoquinoline is of interest in the field of medicinal chemistry due to its potential biological activities and its structural similarity to certain alkaloids found in nature. The synthesis of 3-phenyl-[1,2,4]triazolo[3,4-a]isoquinoline often involves multi-step reactions, and its properties, such as solubility and stability, can be influenced by the presence of various functional groups and substituents. Research on 3-phenyl-[1,2,4]triazolo[3,4-a]isoquinoline and its derivatives may lead to the development of new pharmaceuticals or agrochemicals, highlighting the importance of understanding its chemical structure and reactivity.

3223-55-0

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3223-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3223-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,2 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3223-55:
(6*3)+(5*2)+(4*2)+(3*3)+(2*5)+(1*5)=60
60 % 10 = 0
So 3223-55-0 is a valid CAS Registry Number.

3223-55-0Downstream Products

3223-55-0Relevant academic research and scientific papers

I2-TBHP-catalyzed one-pot highly efficient synthesis of 4,3-fused 1,2,4-triazoles from: N -tosylhydrazones and aromatic N-heterocycles via intermolecular formal 1,3-dipolar cycloaddition

Inturi, Surendra Babu,Kalita, Biswajit,Ahamed, A. Jafar

supporting information, p. 11061 - 11064 (2016/12/07)

I2-TBHP-catalyzed azomethine imine generation and subsequent regioselective 1,3-dipolar cycloaddition (DC) with aromatic N-heterocycles was developed to afford various 4,3-fused 1,2,4-triazoles in excellent yields. The method is operationally simple and highly efficient with broad functional group tolerance.

Synthesis of 1,2,4-Triazolo[4,3-a]pyridines and Related Heterocycles by Sequential Condensation and Iodine-Mediated Oxidative Cyclization

Li, Ertong,Hu, Zhiyuan,Song, Lina,Yu, Wenquan,Chang, Junbiao

, p. 11022 - 11027 (2016/07/27)

A facile and efficient approach to access 1,2,4-triazolo[4,3-a]pyridines and related heterocycles has been accomplished through condensation of readily available aryl hydrazines with corresponding aldehydes followed by iodine-mediated oxidative cyclizatio

Palladium-catalyzed coupling of aldehyde-derived hydrazones: Practical synthesis of triazolopyridines and related heterocycles

Thiel, Oliver R.,Achmatowicz, Michal M.,Reichelt, Andreas,Larsen, Robert D.

supporting information; experimental part, p. 8395 - 8398 (2010/12/25)

The palladium-catalyzed intermolecular coupling of aldehyde-derived hydrazones with chloroazines, followed by oxidative cyclization under mild conditions afforded access to a broad variety of bicyclic heterocyclic scaffolds (see scheme) that have potentia

The Preparation of 3-Phenyltriazolopyridines and Their Benzologs from N-(Phenylsulfonyl)benzohydrazonoyl Chloride and Pyridines

Ito, Suketaka,Kakehi, Akikazu,Matsuno, Toshiyuki,Yoshida, Jun-ichi

, p. 2007 - 2011 (2007/10/02)

3-Phenyltriazolopyridines were obtained in good yields from N'-benzenesulfonohydrazidates, generated from 2-unsubstituted pyridines and N-(phenylsulfonyl)benzohydrazonoyl chloride (2), by oxidation with chloranil.The reaction of quinoline and isoquinoline with 2 gave 1-phenyl-3-phenylsulfonyl-3,3a-dihydrotriazoloquinoline and 3-phenyl-1-phenylsulfonyl-1,10b-dihydrotriazoloisoquinoline respectively, both in good yields; they aromatized to the corresponding triazoles by the 1,2-elimination of benzenesulfinic acid on heating.

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