Tetraethyl [2,2'-bipyridine]-4,4'-diylbis(phosphonate) - 174397-53-6

Tetraethyl [2,2'-bipyridine]-4,4'-diylbis(phosphonate)

Catalog Number: EVT-385184
CAS Number: 174397-53-6
Molecular Formula: C18H26N2O6P2
Molecular Weight: 428.4 g/mol
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Product Introduction

Description
Tetraethyl [2,2'-bipyridine]-4,4'-diylbis(phosphonate) is a chemical compound that has gained significant attention in scientific research due to its potential therapeutic and environmental applications. This paper aims to provide an overview of the synthesis, chemical structure, biological activity, and potential applications of this compound.
Applications in Various Fields
In medical research, tetraethyl [2,2'-bipyridine]-4,4'-diylbis(phosphonate) has shown promise in drug development, particularly in the treatment of cancer and diabetes. Clinical trials are ongoing to evaluate its efficacy and safety in humans. In environmental research, the compound's effects on ecosystems and its potential role in pollution management and sustainability are being studied. In industrial research, tetraethyl [2,2'-bipyridine]-4,4'-diylbis(phosphonate) is being used in manufacturing processes to improve product quality and efficiency. Health and safety considerations must be taken into account when using this compound in industrial settings.

Properties

CAS Number

174397-53-6

Product Name

Tetraethyl [2,2'-bipyridine]-4,4'-diylbis(phosphonate)

IUPAC Name

4-diethoxyphosphoryl-2-(4-diethoxyphosphorylpyridin-2-yl)pyridine

Molecular Formula

C18H26N2O6P2

Molecular Weight

428.4 g/mol

InChI

InChI=1S/C18H26N2O6P2/c1-5-23-27(21,24-6-2)15-9-11-19-17(13-15)18-14-16(10-12-20-18)28(22,25-7-3)26-8-4/h9-14H,5-8H2,1-4H3

InChI Key

BBFROMDCBUIPCU-UHFFFAOYSA-N

SMILES

CCOP(=O)(C1=CC(=NC=C1)C2=NC=CC(=C2)P(=O)(OCC)OCC)OCC

Canonical SMILES

CCOP(=O)(C1=CC(=NC=C1)C2=NC=CC(=C2)P(=O)(OCC)OCC)OCC
Method of Synthesis or Extraction
Tetraethyl [2,2'-bipyridine]-4,4'-diylbis(phosphonate) can be synthesized using various methods, including the reaction of 2,2'-bipyridine with phosphorus oxychloride and tetraethyl orthosilicate. Another method involves the reaction of 2,2'-bipyridine with phosphorus trichloride and triethyl phosphite. The efficiency and yield of each method vary, with the latter method producing a higher yield. However, both methods require careful handling due to the toxicity of the reagents used. Environmental and safety considerations must be taken into account when synthesizing this compound.
Chemical Structure and Biological Activity
Tetraethyl [2,2'-bipyridine]-4,4'-diylbis(phosphonate) has a unique chemical structure that consists of two 2,2'-bipyridine units linked by a phosphonate group. This compound has been shown to exhibit potent biological activity, particularly in the inhibition of protein tyrosine phosphatases (PTPs). PTPs are enzymes that play a crucial role in cell signaling and are involved in various diseases, including cancer and diabetes. Tetraethyl [2,2'-bipyridine]-4,4'-diylbis(phosphonate) has been shown to selectively inhibit PTPs, making it a promising candidate for drug development.
Biological Effects
Tetraethyl [2,2'-bipyridine]-4,4'-diylbis(phosphonate) has been shown to have a significant impact on cell function and signal transduction. Its ability to selectively inhibit PTPs has been linked to its potential therapeutic effects in various diseases. However, the compound's toxicity must be carefully evaluated to avoid potential adverse effects.
Future Perspectives and Challenges
Current limitations in the use and study of tetraethyl [2,2'-bipyridine]-4,4'-diylbis(phosphonate) include its toxicity and potential adverse effects. Possible solutions and improvements include the development of safer and more efficient synthesis methods and the evaluation of its potential therapeutic effects in various diseases. Future trends and prospects in the application of this compound in scientific research include its potential use in personalized medicine and the development of targeted therapies.

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