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6-phenyl-6,7-dihydro-5H-dibenzo[c,e]azepine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13216-36-9

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13216-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13216-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,1 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13216-36:
(7*1)+(6*3)+(5*2)+(4*1)+(3*6)+(2*3)+(1*6)=69
69 % 10 = 9
So 13216-36-9 is a valid CAS Registry Number.

13216-36-9Downstream Products

13216-36-9Relevant academic research and scientific papers

Bimetallic Au-Pd nanochain networks: Facile synthesis and promising application in biaryl synthesis

Wang, Zheng-Jun,Wang, Xia,Lv, Jing-Jing,Feng, Jiu-Ju,Xu, Xinhua,Wang, Ai-Jun,Liang, Zhiwu

, p. 3894 - 3899 (2017)

A simple and facile method is described for the morphology-controlled synthesis of bimetallic Au-Pd alloyed nanochain networks (NNCs) that show high catalytic performance for the Ullmann intermolecular homocoupling of aromatic or alkyl halides (X = I, Br, Cl) in aqueous media and can be reused at least five times, which can also be applied to intramolecular homocoupling.

Synthesis of 6,7-dihydro-5H-dibenzo[c,e]azepines and biaryls by palladium-catalyzed Ullmann reaction

Yu, Ming,Tang, Ri-Yuan,Li, Jin-Heng

experimental part, p. 3409 - 3416 (2009/09/27)

A novel palladium-catalyzed Ullmann protocol is described for the synthesis of 6,7-dihydro-5H-dibenzo[c,e]azepines and biaryls. In the presence of Pd(OAc)2 and KOAc, intramolecular or intermolecular Ullmann coupling of aryl halides proceeds efficiently under ligand-free and aerobic conditions to afford the corresponding 6,7-dihydro-5H-dibenzo[c,e]azepines and biaryls in moderate to excellent yields.

Dicyanomethylene compounds as cyanation reagents

D?pp, Dietrich,Jüschke, Sabine,Henkel, Gerald

, p. 460 - 470 (2007/10/03)

Ethenetetracarbonitrile (2, in benzene solution) and 1,3-dioxoindan-2-ylidene propanedinitrile (4, in ethanol or acetonitrile solution) act on N-aryl-2,3-dihydro-1H-benz[d,e]isoquinolines 6a-d and N-aryl-6,7-dihydro-5H-dibenz[c,e]azepines 11a-d via hydrid

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