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Pyridine, 2,6-bis(4-chlorophenyl)-4-(3-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105372-56-3

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105372-56-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105372-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,7 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 105372-56:
(8*1)+(7*0)+(6*5)+(5*3)+(4*7)+(3*2)+(2*5)+(1*6)=103
103 % 10 = 3
So 105372-56-3 is a valid CAS Registry Number.

105372-56-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-nitrophenyl)-2,6-bis(4-chlorophenyl)pyridine

1.2 Other means of identification

Product number -
Other names 2,6-Bis(4-chlorophenyl)-4-(3-nitrophenyl)pyridine

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:105372-56-3 SDS

105372-56-3Downstream Products

105372-56-3Relevant academic research and scientific papers

Application of salicylic acid as an eco-friendly and efficient catalyst for the synthesis of 2,4,6-triaryl pyridine, 2-amino-3-cyanopyridine, and polyhydroquinoline derivatives

Roozifar, Majid,Hazeri, Nourallah,Faroughi Niya, Homayoun

, p. 1117 - 1129 (2021/02/26)

In this study, three eco-friendly, efficient, and convenient protocols have been reported for one-pot synthesis of 2,4,6-triaryl pyridine, 2-amino-3-cyanopyridine, and polyhydroquinoline derivatives using salicylic acid as a catalyst under solvent-free condition. The reported protocols offer several significant advantages such as the application of a nontoxic, neutral, and cheap catalyst, environmentally friendly conditions, the easy isolation of products by filtering, short reaction times, simple methodology, and good yields.

Synthesis and application of chitosan supported vanadium oxo in the synthesis of 1,4-dihydropyridines and 2,4,6-triarylpyridines: Via anomeric based oxidation

Safaiee, Maliheh,Ebrahimghasri, Bahar,Zolfigol, Mohammad Ali,Baghery, Saeed,Khoshnood, Abbas,Alonso, Diego A.

, p. 12539 - 12548 (2018/08/04)

Chitosan, as a biopolymer, exhibits a strong affinity for complexation with suitable metal ions. Thus, it has received increased attention for the preparation of stable bioorganic-inorganic hybrid heterogeneous catalysts. Herein, a novel chitosan based vanadium oxo (ChVO) catalyst was prepared and fully characterized by several techniques such as Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), thermal gravimetric analysis (TGA), derivative thermal gravimetric (DTG), differential thermal analysis (DTA), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), X-ray photoelectron spectroscopy (XPS) and inductively coupled plasma mass spectrometry (ICP-MS). The synthesized catalyst has been successfully used as a reusable catalyst in the synthesis of dihydropyridines and triarylpyridines.

Three-component one-pot synthesis of 2,4,6-triarylpyridines without catalyst and solvent

Wang, Min,Yang, Zhongyong,Song, Zhiguo,Wang, Qinglin

, p. 907 - 910 (2015/05/13)

An efficient and green synthesis of 2,4,6-triarylpyridines by a one-pot three-component condensation of aromatic aldehydes, substituted acetophenones, and ammonium acetate without catalyst at 130°C under solvent-free conditions is described. This method offers several advantages such as simple procedure, easy work-up, short reaction time, low cost, environmentally friendly conditions, and moderate to high yields.

Synthesis of Some New 2,4,6-Triarylpyridines Using Phenacylidenedimethylsulfuranes

Gupta, Komal C.,Pathak, Pankaj K.,Saxena, Brijesh K.,Srivastava, Nirupma,Pandey, Kalpna

, p. 131 - 132 (2007/10/02)

Phenacylidenedimethylsulfurane and p-chlorophenacylidenedimethylsulfurane were reacted with α,β-unsaturated ketones in the presence of ammonium acetate in glacial acetic acid to give 2,4,6-triarylpyridines in 45-70percent yields.The structures of the pyri

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