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3-(3-Pyridinyl)benzonitrile is an organic compound with the chemical formula C12H8N2. It is a white crystalline solid that is soluble in organic solvents. 3-(3-PYRIDINYL)BENZONITRILE is characterized by a benzene ring with a nitrile group (-CN) attached to the 3-position and a pyridine ring attached to the same position. The pyridine ring itself has a nitrogen atom at the 3-position, which contributes to its chemical properties. 3-(3-Pyridinyl)benzonitrile is used in the synthesis of various pharmaceuticals and agrochemicals due to its potential to form complex molecular structures. It is also a building block for the creation of more complex organic molecules, making it a valuable intermediate in the field of organic chemistry.

4350-54-3

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4350-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4350-54-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,5 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4350-54:
(6*4)+(5*3)+(4*5)+(3*0)+(2*5)+(1*4)=73
73 % 10 = 3
So 4350-54-3 is a valid CAS Registry Number.

4350-54-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(pyridine-3-yl)benzonitrile

1.2 Other means of identification

Product number -
Other names 3-(pyridin-3-yl)benzonitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4350-54-3 SDS

4350-54-3Downstream Products

4350-54-3Relevant academic research and scientific papers

Efficient phosphine ligands for the one-pot palladium-catalyzed borylation/Suzuki-Miyaura cross-coupling reaction

Chen, You,Peng, Hui,Pi, Yun-Xiao,Meng, Tong,Lian, Ze-Yu,Yan, Meng-Qi,Liu, Yan,Liu, Sheng-Hua,Yu, Guang-Ao

supporting information, p. 3236 - 3242 (2015/03/18)

We report the synthesis of 2-(anthracen-9-yl)-1H-inden-3-yl dicyclohexylphosphine and its use in palladium-catalyzed borylation/Suzuki-Miyaura cross-coupling reaction to prepare a variety of symmetrical and unsymmetrical biaryl compounds in excellent yield. This journal is

Arylation of pyridines via suzuki-miyaura cross-coupling and pyridine-directed C-H activation using a continuous-flow approach

Christakakou, Maria,Sch?n, Michael,Schnürch, Michael,Mihovilovic, Marko D.

supporting information, p. 2411 - 2418 (2013/11/06)

Suzuki-Miyaura cross-coupling reactions between heteroaryl bromides and arylboronic acids were performed employing a continuous-flow approach using a simple flow reactor designed in-house. Pd(PPh3)4 was used as catalyst, and arylboronic acids containing both electron-withdrawing and electron-donating groups were applied. The coupling process required 23 minutes of residence time to be completed and generally good yields were obtained. Subsequent arylation of 2-phenyl pyridine was carried out via a C-H activation strategy using substituted bromobenzene compounds and a ruthenium(II) catalyst. To the best of our knowledge in this work we present for the first time the possibility of performing intermolecular C-H activation in a continuous-flow system. Georg Thieme Verlag Stuttgart, New York.

Scope of the two-step, one-pot palladium-catalyzed borylation/Suzuki cross-coupling reaction utilizing bis-boronic acid

Molander, Gary A.,Trice, Sarah L. J.,Kennedy, Steven M.

, p. 8678 - 8688 (2012/11/07)

The use of bis-boronic acid for the direct synthesis of boronic acids has greatly facilitated the two-step, one-pot borylation/Suzuki cross-coupling reaction between aryl and heteroaryl halides. With use of Buchwald's second-generation XPhos preformed catalyst, high yields of cross-coupled products were obtained for most substrates. The method also allows an efficient two-step, one-pot synthesis, providing access to three distinct cross-coupled products after column chromatography. The method also provides a rapid and convenient route to teraryl compounds.

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