1560-55-0 Usage
Description
ETHYL-2,2,2-D3-TRIPHENYLPHOSPHONIUM BROMIDE, with the CAS number 1560-55-0, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. It is a derivative of the triphenylphosphonium cation, which is known for its unique properties and potential applications in different fields.
Uses
Used in Research and Development:
ETHYL-2,2,2-D3-TRIPHENYLPHOSPHONIUM BROMIDE is used as a research compound for its isotopically labeled nature, allowing scientists to study and understand the behavior of this compound in various chemical reactions and processes. The application reason is to facilitate the investigation of its properties and potential uses in different scientific fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ETHYL-2,2,2-D3-TRIPHENYLPHOSPHONIUM BROMIDE is used as a starting material or intermediate in the synthesis of various pharmaceutical compounds. The application reason is its unique chemical structure, which can be modified and utilized to create new drugs with potential therapeutic benefits.
Used in Chemical Synthesis:
ETHYL-2,2,2-D3-TRIPHENYLPHOSPHONIUM BROMIDE is used as a reagent in chemical synthesis, particularly in the preparation of complex organic molecules. The application reason is its ability to participate in various chemical reactions, such as substitution, addition, and elimination reactions, making it a versatile compound for synthetic purposes.
Used in Material Science:
In the field of material science, ETHYL-2,2,2-D3-TRIPHENYLPHOSPHONIUM BROMIDE is used as a component in the development of new materials with specific properties. The application reason is its potential to contribute to the creation of materials with unique electronic, optical, or mechanical properties, which can be applied in various industries, such as electronics, energy, and aerospace.
Used in Environmental Science:
ETHYL-2,2,2-D3-TRIPHENYLPHOSPHONIUM BROMIDE is used as a tracer or marker in environmental studies, helping researchers to track and understand the behavior of pollutants or contaminants in the environment. The application reason is its isotopically labeled nature, which allows for easy detection and monitoring of its presence in various environmental samples.
Check Digit Verification of cas no
The CAS Registry Mumber 1560-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1560-55:
(6*1)+(5*5)+(4*6)+(3*0)+(2*5)+(1*5)=70
70 % 10 = 0
So 1560-55-0 is a valid CAS Registry Number.
1560-55-0Relevant articles and documents
Cyclopropane Intermediates in the Rearrangemant and Fragmentation of Olefinic Molecular Ions
Laderoute, Keith R.,Harrison, Alex. G.
, p. 624 - 630 (1985)
Methyl loss from deuterium-labelled molecular ions of 4-methyl-2-pentene, 2-methyl-2-pentene and 1,1,2-trimethylcyclopropane has been investigated for metastable molecular ions and for molecular ions formed by charge exchange with COS+*, XE+* and CO+*.For metastable ion fragmentation reactions all three compounds exhibit very similar behavior and show specific and essentially equal loss of each of the original methyl groups as well as specific loss of a methyl where the hydrogens derive exclusively from the non-methyl hydrogens of the original molecules.The former results are interpreted in terms of interconversion of the three molecular ions through a ring-opened form of the trimethylcyclopropane molecular ion.The loss of the non-methyl hydrogens as CH3 is interpreted in terms of isomerization to the 2,3-dimethyl-2-butene structure.With increasing internal energy direct allylic cleavage of the unrearranged methylpentene molecular ions increases in importance while the trimethylcyclopropane molecular ion shows an increased preference for loss of the C(2) methyl group.With increasing internal energy loss of the original non-methyl hydrogens as CH3 decreases markedly in importance.
