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2-phenylpyrrolo[2,1-a]isoquinoline is a complex organic compound with the molecular formula C19H13N. It is a heterocyclic molecule that features a pyrroloisoquinoline core, which consists of a pyrrole ring fused to an isoquinoline ring. The "2-phenyl" part of the name indicates that there is a phenyl group (a benzene ring) attached to the second carbon of the pyrroloisoquinoline structure. 2-phenylpyrrolo[2,1-a]isoquinoline is of interest in the field of organic chemistry and may have potential applications in the development of pharmaceuticals or other chemical products due to its unique structure and properties. However, it is important to note that the specific uses, safety, and environmental impact of 2-phenylpyrrolo[2,1-a]isoquinoline would require further research and evaluation.

7496-93-7

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7496-93-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7496-93-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,9 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7496-93:
(6*7)+(5*4)+(4*9)+(3*6)+(2*9)+(1*3)=137
137 % 10 = 7
So 7496-93-7 is a valid CAS Registry Number.

7496-93-7Downstream Products

7496-93-7Relevant academic research and scientific papers

Synthesis of functionalized indolizines via copper-catalyzed annulation of 2-alkylazaarenes with α,β-unsaturated carboxylic acids

Yang, Yuzhu,Xie, Chunsong,Xie, Yongju,Zhang, Yuhong

supporting information; experimental part, p. 957 - 959 (2012/04/04)

A novel copper-catalyzed annulation of 2-alkylazaarenes with α,β-unsaturated carboxylic acids has been accomplished. This reaction featuring C-H olefination and decarboxylative amination processes provides a concise access to C-2 arylated indolizines from simple and readily available starting materials.

Reaction of 1-Methyl-3,4-dihydroisoquinoline with Phenacyl Bromides

Nair, M. D.,Desai, J. A.

, p. 65 - 66 (2007/10/02)

The reaction of 1-methyl-3,4-dihydroisoquinoline with phenacyl bromide and phenyl substituted phenacyl bromides have been carried out.The structure of the product of phenacyl bromide reaction has been unambiguously assigned as 5,6-dihydro-2-phenylpyrrolo

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