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2,2'-Bipyridine, 4,4'-bis(phenylmethyl)-, also known as 4,4'-Bis(benzyl)-2,2'-bipyridine, is an organic compound with the chemical formula C22H20N2. It is a white crystalline solid that is soluble in common organic solvents such as ethanol, acetone, and dichloromethane. 2,2'-Bipyridine, 4,4'-bis(phenylmethyl)- is a derivative of bipyridine, featuring two benzyl groups attached to the 4,4' positions of the bipyridine core. It is often used as a ligand in coordination chemistry, particularly in the formation of metal complexes, due to its ability to chelate metal ions through its nitrogen atoms. The compound is also of interest in the field of supramolecular chemistry and has potential applications in the development of new materials and catalysts.

1762-38-5

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1762-38-5 Usage

Properties

Chemical compound
Commonly used as a ligand in coordination chemistry
Bidentate ligand
Coordinates with a metal ion using two of its nitrogen atoms

Specific content

Used in organometallic chemistry
Acts as a catalyst in various chemical processes
Stabilizes metal complexes
Facilitates catalytic reactions
Studied for potential applications in organic synthesis and material science
Versatile and important chemical compound in various areas of chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 1762-38-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,6 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1762-38:
(6*1)+(5*7)+(4*6)+(3*2)+(2*3)+(1*8)=85
85 % 10 = 5
So 1762-38-5 is a valid CAS Registry Number.

1762-38-5Upstream product

1762-38-5Downstream Products

1762-38-5Relevant academic research and scientific papers

Substituted 2,2'-bipyridyl compounds and process for preparing same

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, (2008/06/13)

A process for preparing substituted 2,2'-bipyridyl compounds and several compounds so prepared, the process comprising the steps of first selecting a substituted pyridine of the formula defined herein, then mixing a stoichiometric excess of the substituted pyridine with an amount of sodamide, causing the resultant mixture to be at a temperature sufficiently high to cause substituted 2,2'-bipyridyl formation, and isolating the substituted 2,2'-bipyridyl thereby formed. The new substituted 2,2'-bipyridyl compounds are selected from the group consisting of 4,4'-di-(5-nonyl)-2,2'-bipyridyl; 4,4'-di-(3-pentyl)-2,2'-bipyridyl; 6,6'-di-(3-pentyl)-2,2'-bipyridyl; 6,6'-di-(5-nonyl)-2,2'-bipyridyl; 4,4'-di-(cyclohexylmethyl)-2,2'-bipyridyl; 5,5'-di-(5-nonyl)-2,2'-bipyridyl; 4,4'-di-(3-phenylpropyl)-2,2'-bipyridyl; 4,4'-di-(4-tetrahydropyranyl)-2,2'-bipyridyl; 4,4'-di-benzyl-2,2'-bipyridyl; 6,6'-di-isoamyl-2,2'-bipyridyl; and 4,4'-di-(t-butyl)-2,2'-bipyridyl.

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