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2H-Quinolizine, octahydro-4-phenyl, trans- is a complex organic compound with the molecular formula C15H21N. It is a derivative of quinolizine, a bicyclic aromatic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrolidine ring. The octahydro prefix indicates that the compound has undergone hydrogenation, resulting in the saturation of its double bonds. The 4-phenyl substitution refers to a phenyl group (C6H5) attached to the fourth carbon of the quinolizine ring. The trans- configuration denotes that the phenyl group is positioned across from the nitrogen atom in the bicyclic structure. 2H-Quinolizine, octahydro-4-phenyl-, trans- is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or materials science due to its unique structure and properties.

3238-66-2

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3238-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3238-66-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,3 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3238-66:
(6*3)+(5*2)+(4*3)+(3*8)+(2*6)+(1*6)=82
82 % 10 = 2
So 3238-66-2 is a valid CAS Registry Number.

3238-66-2Downstream Products

3238-66-2Relevant academic research and scientific papers

Cyclizations and cycloadditions of acetylenic sulfones on solid supports

Back, Thomas G.,Zhai, Huimin

, p. 326 - 328 (2008/02/08)

Acetylenic sulfones attached to solid supports by means of ester linkers were employed in a variety of cyclization and cycloaddition reactions, followed by cleavage of the products from the resin by ester hydrolysis or reductive desulfonylation. The Royal

A Schmidt route to 1-azabicyclo[x.y.0]alkanes: A comparison of carbocation stabilizing groups

Pearson, William H,Walavalkar, Rajesh

, p. 5081 - 5089 (2007/10/03)

The intramolecular Schmidt reactions of tertiary alkyl, tertiary benzylic, tertiary propargylic, and tertiary allylic carbocations with tethered azides are reported. Using product analysis and deuterium labeling studies, the role of cation rearrangement p

Synthesis of 4-Phenyl-1,2,3,4-tetrahydroquinolizinium Salts and Their Hydrogenated Derivatives

Czarnocki, Zbigniew,Wrobel, Jerzy T.

, p. 201 - 210 (2007/10/02)

A new method of construction of quinolizidine nucleus is described.Olefinic compounds 1-4 upon hydrogen bromide addition cyclized into quinolizinium salts 5-8 which after hydrogenation yielded quinolizidines 5a-8a.Stereochemistry of all compounds obtained

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