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2-([1,1':3',1''-terphenyl]-4'-yl)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1374451-74-7

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1374451-74-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1374451-74-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,4,4,5 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1374451-74:
(9*1)+(8*3)+(7*7)+(6*4)+(5*4)+(4*5)+(3*1)+(2*7)+(1*4)=167
167 % 10 = 7
So 1374451-74-7 is a valid CAS Registry Number.

1374451-74-7Downstream Products

1374451-74-7Relevant academic research and scientific papers

Cascade 8πElectrocyclization/Benzannulation to Access Highly Substituted Phenylpyridines

Du, Luan,Gong, Yiliang,Han, Jingpeng,Li, Baosheng,Li, You,Luo, Han,Tian, Yi,Xin, Xiaolan

, p. 7966 - 7971 (2021/10/25)

A cascade 8πelectrocyclization/benzannulation reaction was developed to obtain the synthetically important highly substituted phenyl-pyridines. This method shows great potential in the rapid and inexpensive application of the scalable and operationally simple production of accessible substrates. On the basis of the resulting phenyl-pyridine products, a new Ru catalyst and bidentate ligand were designed and prepared, further demonstrating its high practicability.

Group exchange between ketones and carboxylic acids through directing group assisted Rh-catalyzed reorganization of carbon skeletons

Lei, Zhi-Quan,Pan, Fei,Li, Hu,Li, Yang,Zhang, Xi-Sha,Chen, Kang,Wang, Xin,Li, Yu-Xue,Sun, Jian,Shi, Zhang-Jie

supporting information, p. 5012 - 5020 (2015/05/05)

The Rh(I)-catalyzed direct reorganization of organic frameworks and group exchanges between carboxylic acids and aryl ketones was developed with the assistance of directing group. Biaryls, alkenylarenes, and alkylarenes were produced in high efficiency from aryl ketones and the corresponding carboxylic acids by releasing the other molecule of carboxylic acids and carbon monoxide. A wide range of functional groups were well compatible. The exchanges between two partners were proposed to take place on the Rh-(III) center of key intermediates, supported by experimental mechanistic studies and computational calculations. The transformation unveiled the new catalytic pathway of the group transfer of two organic molecules.

Extrusion of CO from aryl ketones: Rhodium(I)-catalyzed C-C bond cleavage directed by a pyridine group

Lei, Zhi-Quan,Li, Hu,Li, Yang,Zhang, Xi-Sha,Chen, Kang,Wang, Xin,Sun, Jian,Shi, Zhang-Jie

supporting information; experimental part, p. 2690 - 2694 (2012/04/23)

Snipping tool: The rhodium(I)-catalyzed extrusion of carbon monoxide from biaryl ketones and alkyl/alkenyl aryl ketones was developed to produce biaryls and alkyl/alkenyl arenes, respectively, in high yields (see scheme). A wide range of functionalities are tolerated. Not only does this method provide an alternative pathway to construct useful scaffolds, but also offers a new strategy for C-C bond activation. Copyright

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