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4-(1,3-dipyridin-4-ylpropan-2-yl)pyridine is a complex organic compound with the molecular formula C20H17N3. It is characterized by a pyridine ring at the core, with a propane-2-yl chain connecting two additional pyridine rings, one of which is substituted at the 4-position. This molecule is known for its potential applications in the field of coordination chemistry, particularly as a ligand in the formation of metal complexes. Its structure allows for the creation of stable complexes with various metal ions, making it a subject of interest in research related to supramolecular chemistry and materials science. The compound's unique structure and properties also make it a candidate for further exploration in the development of new pharmaceuticals and other specialty chemicals.

5421-79-4

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5421-79-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5421-79-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5421-79:
(6*5)+(5*4)+(4*2)+(3*1)+(2*7)+(1*9)=84
84 % 10 = 4
So 5421-79-4 is a valid CAS Registry Number.

5421-79-4SDS

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-(1,3-dipyridin-4-ylpropan-2-yl)pyridine

1.2 Other means of identification

Product number -
Other names 1,2,3-Tri-[4]pyridyl-propan

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:5421-79-4 SDS

5421-79-4Upstream product

5421-79-4Downstream Products

5421-79-4Relevant academic research and scientific papers

Impurity in tirofiban material, preparation of impurity, and method for detecting impurity in material

-

Paragraph 0055; 0058; 0059; 0060; 0061, (2018/09/12)

The invention discloses an impurity in a tirofiban material, preparation of the impurity, and a method for detecting the impurity in the material. The impurity is a compound shown in a formula I, wherein R is selected from the following substituents: hydrogen, halogen, cyano group, amino, nitro, aryl and ceteroary; the R further is hydrogen or pyridyl. The method plays an important practical rolein improvement of the quality of the tirofiban and control of the safety of the tirofiban form the origin.

Nitro-methyl redox coupling: Efficient approach to 2-hetarylbenzothiazoles from 2-halonitroarene, methylhetarene, and elemental sulfur

Nguyen, Thanh Binh,Ermolenko, Ludmila,Al-Mourabit, Ali

supporting information, p. 4218 - 4221 (2013/09/12)

A simple, straightforward, and atom economic approach to 2-hetarylbenzothiazoles starting from 2-halonitroarene, methylhetarene, and elemental sulfur under mild conditions is described. The method is highlighted by the direct redox nitro-methyl reaction for carbon-nitrogen bond formation without an added oxidizing or reducing agent.

ELEMENTAL SULFUR REACTIONS WITH 4-PICOLINE

Gleich Z.,Warnke, Z.,Szafranek, J.,Malinski, E.

, p. 315 - 326 (2007/10/02)

A study of the reaction of the elemental sulfur with 4-picoline is reported.The process was carried out at the boiling point of the 4-picoline under argon.After removing unreacted solids, the reaction products were identified by means of LC, GC, and GC-MS

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