88278-22-2 Usage
Uses
Used in Organic Synthesis:
Trimethylphenylammonium-d9 Iodide is used as a reagent in organic synthesis for its unique properties. The incorporation of deuterium atoms provides enhanced stability and reactivity, which can be advantageous in specific chemical reactions. This makes it a valuable component in the synthesis of various organic compounds, particularly those requiring isotopically labeled molecules for research purposes.
Used in Research Applications:
In the field of research, Trimethylphenylammonium-d9 Iodide serves as a useful probe for studying reaction mechanisms and kinetics. The presence of deuterium atoms allows for the investigation of isotope effects, which can provide insights into the behavior of molecules and the pathways of chemical reactions. Trimethylphenylammonium-d9 Iodide can be particularly useful in studies involving isotopically sensitive reactions or in the development of new synthetic methodologies.
Used in Pharmaceutical Industry:
Trimethylphenylammonium-d9 Iodide can be employed in the pharmaceutical industry for the synthesis of isotopically labeled drug candidates. These labeled compounds are essential for understanding drug metabolism, pharmacokinetics, and pharmacodynamics. Additionally, they can be used in the development of new drugs, where the incorporation of deuterium can potentially improve the stability, solubility, or bioavailability of the drug molecule.
Used in Analytical Chemistry:
In analytical chemistry, Trimethylphenylammonium-d9 Iodide can be utilized as an internal standard or a reference compound in various analytical techniques. The presence of deuterium atoms can help in the accurate quantification and identification of target compounds, particularly in mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. This application is crucial for ensuring the reliability and precision of analytical results.
Check Digit Verification of cas no
The CAS Registry Mumber 88278-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,7 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88278-22:
(7*8)+(6*8)+(5*2)+(4*7)+(3*8)+(2*2)+(1*2)=172
172 % 10 = 2
So 88278-22-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N.HI/c1-10(2,3)9-7-5-4-6-8-9;/h4-8H,1-3H3;1H/q+1;/p-1/i1D3,2D3,3D3;
88278-22-2Relevant academic research and scientific papers
REACTION OF NUCLEOPHILES WITH ELECTRON ACCEPTORS BY SN2 OR ELECTRON TRANSFER (ET) MECHANISMS: TERT-BUTYL PEROXYBENZOATE/DIMETHYL SULFIDE AND BENZOYL PEROXIDE/N,N-DIMETHYLANILINE SYSTEMS.
Pryor,Hendrickson Jr.
, p. 7114 - 7122 (2007/10/02)
This study is one of a series that probes the reactions of nucleophiles with peroxides, reactions that can occur either by an initial S//N2 reaction or by an electron-transfer (ET) reaction. The products and kinetics are reported for the reaction of dimethyl sulfide and a series of ring-substituted aryl methyl sulfides with tert-butyl peroxybenzoate (TBP) and four ring-substituted TPB's. Kinetic analysis allows the separation of the rate constants for unimolecular homolysis (k//1) and those for the decomposition of the TBP by the sulfide (k//2). The bimolecular reaction is accelerated by electron-withdrawing substituents in the TBP; for example, when 3,5-(NO//2)//2-TBP is used, k//2/k//1 is 12,000. The products that are formed are consistent with a radical process; however, this evidence is not regarded as conclusive.
