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5368-60-5

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5368-60-5 Usage

Description

(Oxydimethanediyl)bis(triphenylphosphonium) is a phosphonium salt with the molecular formula C42H36O2P2. It is a chemical compound that is utilized in organic synthesis and serves as a catalyst in various chemical reactions. (oxydimethanediyl)bis(triphenylphosphonium) is recognized for its capability to efficiently transfer phosphonium groups, which has led to its use in the development of phosphorus-containing drugs and materials. Its phosphonium group also exhibits strong antimicrobial activity against various pathogens, making it a potential candidate for further research and application in the fields of chemistry and biochemistry.

Uses

Used in Organic Synthesis:
(Oxydimethanediyl)bis(triphenylphosphonium) is used as a catalyst in organic synthesis for facilitating various chemical reactions. Its phosphonium group enhances the efficiency of these reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (oxydimethanediyl)bis(triphenylphosphonium) is used as a key component in the development of phosphorus-containing drugs and materials. Its ability to transfer phosphonium groups makes it a promising candidate for creating novel therapeutic agents with potential applications in treating various diseases.
Used in Advanced Electronic Materials Production:
(Oxydimethanediyl)bis(triphenylphosphonium) is also utilized in the production of advanced electronic materials. Its unique properties contribute to the development of innovative materials with enhanced performance characteristics for use in the electronics industry.
Used in Chemical Research:
As a reagent, (oxydimethanediyl)bis(triphenylphosphonium) is employed in chemical research to study its properties and potential applications. Further research is needed to fully understand and harness its potential in different fields of chemistry and biochemistry.
Used in Antimicrobial Applications:
Due to its phosphonium group, (oxydimethanediyl)bis(triphenylphosphonium) has shown strong antimicrobial activity against various pathogens. It is used as a potential antimicrobial agent in the development of new treatments and products to combat resistant infections and improve public health. However, more research is required to fully explore and optimize its antimicrobial potential.

Check Digit Verification of cas no

The CAS Registry Mumber 5368-60-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5368-60:
(6*5)+(5*3)+(4*6)+(3*8)+(2*6)+(1*0)=105
105 % 10 = 5
So 5368-60-5 is a valid CAS Registry Number.

5368-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenyl(triphenylphosphaniumylmethoxymethyl)phosphanium,bromide

1.2 Other means of identification

Product number -
Other names Bis-<triphenyl-phosphoniomethyl>-ether-dibromid

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:5368-60-5 SDS

5368-60-5Relevant articles and documents

Diferrocenyl molecular wires. the role of heteroatom linkers

Li, Yu,Josowicz, Mira,Tolbert, Laren M.

supporting information; experimental part, p. 10374 - 10382 (2010/09/06)

Diferrocenyl molecular "wires", in which two ferrocenes are linked by a conjugated chain, allowing the communication of redox information between the ferrocenes, are a versatile platform on which to investigate notions of molecular conductivity. In this paper, we examine the role of heteroatoms=including O, P, S, and Se, as well as C atoms in various oxidation states=separated from the ferrocenes by intervening double bonds which minimize any steric effects. Surprisingly, oxygen is a better electronic mediator than sulfur, a phenomenon we attribute to superior molecular orbital overlap. These fundamental studies on redox coupling will help to guide the design of efficient organic conductors for organic electronics.

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