3669-69-0 Usage
Uses
Used in Research and Development:
N-METHYLACETAMIDE-2,2,2-D3 is used as an isotopically labeled compound for research purposes. The incorporation of deuterium in the molecule allows for the study of its unique properties and behavior in various chemical reactions and biological processes. This can be particularly useful in understanding the compound's role in different applications and its potential for further development.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-METHYLACETAMIDE-2,2,2-D3 is used as a research tool to investigate the effects of isotopic substitution on drug metabolism, pharmacokinetics, and pharmacodynamics. This information can be crucial in the development of new drugs and the optimization of existing ones, as it can help identify potential side effects, improve drug efficacy, and reduce the risk of drug resistance.
Used in Chemical Synthesis:
N-METHYLACETAMIDE-2,2,2-D3 can also be used as a starting material or intermediate in the synthesis of other deuterated compounds. The presence of deuterium in the molecule can affect the reaction rates and pathways, making it a valuable tool for studying reaction mechanisms and developing new synthetic methods.
Used in Analytical Chemistry:
In analytical chemistry, N-METHYLACETAMIDE-2,2,2-D3 can be employed as an internal standard or reference compound for the quantification and identification of related compounds in complex mixtures. The isotopic labeling provides a distinct signature that can be easily distinguished from other components, allowing for accurate and precise measurements.
Used in Environmental Studies:
N-METHYLACETAMIDE-2,2,2-D3 can be utilized in environmental research to study the fate and transport of the compound and its derivatives in various ecosystems. The isotopic labeling can help track the compound's movement and interactions with other components in the environment, providing valuable information for assessing its potential impact on ecosystems and human health.
Check Digit Verification of cas no
The CAS Registry Mumber 3669-69-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,6 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3669-69:
(6*3)+(5*6)+(4*6)+(3*9)+(2*6)+(1*9)=120
120 % 10 = 0
So 3669-69-0 is a valid CAS Registry Number.
3669-69-0Relevant academic research and scientific papers
Stereodynamics of Diethylmethylamine and Triethylamine
Bushweller, C. Hackett,Fleischman, Stephen H.,Grady, Gilbert L.,McGoff, Paul,Rithner, Christopher D.,et al.
, p. 6224 - 6236 (2007/10/02)
Diethylamine is the simplest acyclic trialkylamine that possesses the requisite symmetry that allows, in principle, the direct observation of both nitrogen inversion and isolated nitrogen-carbon bond rotation using 1H dynamic nuclear magnetic resonance (DNMR) spectroscopy.DNMR studies of diethylmethylamine and two deuterated derivatives complemented by empirical force-field calculations reveal a comprehensive picture of the stereodynamics of this representative acyclic trialkylamine.The DNMR studies show clear evidence for pyramidal inversion at nitrogen.In addition to nitrogen inversion, the results also speak for several "families" of rotamers for diethylmethylamine that undergo very rapid, DNMR-invisible intrafamily conformational exchange via isolated N-CH2 rotation while also undergoing higher barrier DNMR-visible interfamily exchange also via isolated N-CH2 rotation.The DNMR-visible N-CH2 rotation processes involve CCH3/N-alkyl eclipsing in the transition state while the DNMR-invisible processes involve CCH3/lone pair eclipsing.Although the symmetry of triethylamine precludes the DNMR-observation of nitrogen inversion, (1)H DNMR evidence for restricted N-CH2 rotation and empirical force-field calculations reveal stereodynamics for triethylamine that are highly analogous to diethylmethylamine.
