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Cobalt, trimethylphosphanium, and triphenyltin are three distinct chemical substances with unique properties and applications. Cobalt is a metallic element known for its industrial and medical uses, while trimethylphosphanium is an organophosphorus compound that serves as a ligand in coordination chemistry. Triphenyltin, a chemical compound composed of tin and phenyl groups, is commonly used as a pesticide and in organic synthesis. These chemicals contribute to various fields, including industrial manufacturing, medical applications, and laboratory research.

7242-95-7

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7242-95-7 Usage

Uses

Used in Industrial Manufacturing:
Cobalt is used as a key component in the production of various alloys, magnets, and batteries due to its magnetic and catalytic properties. Its ability to enhance hardness and strength makes it valuable in the manufacturing of cutting tools, aircraft engines, and other high-performance applications.
Trimethylphosphanium is used as a ligand in coordination chemistry for the synthesis of metal complexes. Its electron-donating properties enable the formation of stable complexes with various metal ions, which are useful in catalysis, materials science, and pharmaceutical applications.
Triphenyltin is used as a pesticide in agriculture to control pests and protect crops. Its biocidal properties make it effective against a wide range of insects, fungi, and other organisms that can damage crops and reduce yields.
Used in Medical Applications:
Cobalt is used in the medical field for its radioisotope, cobalt-60, which is employed in radiation therapy to treat cancer. Its ability to emit gamma radiation allows for targeted destruction of cancer cells while minimizing damage to surrounding healthy tissue.
Used in Laboratory Research:
Trimethylphosphanium is used as a ligand in coordination chemistry for the study of metal complexes and their properties. Its ability to form stable complexes with metal ions facilitates research in areas such as catalysis, materials science, and the development of new pharmaceutical compounds.
Triphenyltin is used in organic synthesis for the preparation of various organic compounds, including pharmaceuticals, dyes, and polymers. Its reactivity with organic substrates allows for the formation of new chemical bonds and the synthesis of complex molecules for research purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 7242-95-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,4 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7242-95:
(6*7)+(5*2)+(4*4)+(3*2)+(2*9)+(1*5)=97
97 % 10 = 7
So 7242-95-7 is a valid CAS Registry Number.

7242-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name cobalt(2+),trimethylphosphanium,triphenylstannanylium

1.2 Other means of identification

Product number -
Other names trimethylphosphanium

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:7242-95-7 SDS

7242-95-7Downstream Products

7242-95-7Relevant academic research and scientific papers

The Synthesis of 7-anti-Substituted 2-exo- and 2-endo-Norbornanols

Flury, Peter,Grob, Cyril A.

, p. 1991 - 2001 (2007/10/02)

The title compounds and the corresponding p-toluenesulfonates were prepared in connection with a mechanistic study of C-participation in carbocations.

Stereochemistry of acid-catalyzed cleavage of 3-chloro- and 3-bromonortricyclene in deuterated medium. Evidence for edge protonation of nortricyclenes

Werstiuk, Nick Henry,Timmins, George,Cappelli, Frank Peter

, p. 1709 - 1724 (2007/10/02)

Cleavage of 3-chloronortricyclene (4c) and 3-bromonortricyclene (4d) occurs faster than solvolysis in D2SO4-DOAc at 70-75 deg C and yields syn-7-, anti-7-, exo-5-, and endo-5-halo-exo-2-norbornyl acetates as products.That the 7-chloroacetates comprise 70percent of the reaction mixture, that 30percent of the 5-chloro-exo-2-norbornyl acetates which comprised 28percent of the reaction mixture are derived via rearrangement of the syn-7- and anti-7-chloronorbornyl cations, and that the deuterium at C-6 is at least 90percent stereochemically pure endo is evidence that cleavage of the bond farthest removed from the electron withdrawing halogen is preferred 5:1 over the other bonds of the three-membered ring.The stereochemistry of the ring-opening is rationalized on the basis of cleavage via edge-deuteronation with formation of classical halocations as intermediates.The location of deuterium in the 5-halo-exo-norbornyl acetates is used to define the pathways whereby the 5-haloacetates are formed.This study also establishes that C-6 endo deuterated 7-chloro- and 7-bromo-exo-2-norbornyl brosylates can be synthesized from the corresponding 3-halonortricyclenes.

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