357407-86-4 Usage
Description
(R)-(+)-N-METHYL-1-PHENYLETHYLAMINE-D13 is a deuterated form of the chemical N-methyl-1-phenylethylamine, an organic compound belonging to the amphetamine class. As a chiral molecule, it possesses a non-superimposable mirror image and contains additional deuterium atoms in its deuterated form. (R)-(+)-N-METHYL-1-PHENYLETHYLAMINE-D13 is primarily utilized in chemical research, allowing for the study of amphetamine derivatives' behavior and properties in biological and chemical systems. The presence of deuterium atoms enables more accurate analysis through spectroscopy and other analytical techniques.
Uses
Used in Chemical Research:
(R)-(+)-N-METHYL-1-PHENYLETHYLAMINE-D13 is used as a reagent for studying the behavior and properties of amphetamine derivatives in various chemical and biological systems. Its deuterated form provides enhanced precision in analysis, making it a valuable tool in the field of chemical research.
Used in Spectroscopic Analysis:
In the field of spectroscopy, (R)-(+)-N-METHYL-1-PHENYLETHYLAMINE-D13 is employed as a compound that allows for more accurate and reliable results. The presence of deuterium atoms in its structure improves the signal-to-noise ratio and overall sensitivity of the analytical techniques, leading to better data quality and interpretation.
Used in Pharmaceutical Development:
(R)-(+)-N-METHYL-1-PHENYLETHYLAMINE-D13 can be utilized in the development of new pharmaceuticals, particularly those targeting the amphetamine class of compounds. Its unique properties and deuterated form can aid in understanding the interactions and effects of these compounds on biological systems, potentially leading to the creation of more effective and safer medications.
Used in Material Science:
In material science, (R)-(+)-N-METHYL-1-PHENYLETHYLAMINE-D13 may be employed to study the interactions between amphetamine derivatives and various materials. This can be particularly useful in the development of sensors, coatings, or other materials that require a specific interaction with these types of compounds.
Used in Environmental Studies:
(R)-(+)-N-METHYL-1-PHENYLETHYLAMINE-D13 can also be used in environmental studies to understand the behavior and fate of amphetamine derivatives in the environment. This knowledge can help in assessing the potential risks and impacts of these compounds on ecosystems and developing strategies for their mitigation.
Check Digit Verification of cas no
The CAS Registry Mumber 357407-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,4,0 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 357407-86:
(8*3)+(7*5)+(6*7)+(5*4)+(4*0)+(3*7)+(2*8)+(1*6)=164
164 % 10 = 4
So 357407-86-4 is a valid CAS Registry Number.
357407-86-4Relevant articles and documents
Toward the creation of NMR databases in chiral solvents for assignments of relative and absolute stereochemistry: proof of concept.
Kobayashi,Hayashi,Tan,Kishi
, p. 2245 - 2248 (2001)
[structure: see text] An NMR database approach in a chiral solvent allows us to predict both relative and absolute stereochemistry of an unknown compound without degradation and/or derivatization. N,alpha-Dimethylbenzylamine (DMBA) is a suitable solvent for this purpose. Using the C.5-C.10 portion of oasomycin A, the feasibility and reliability of this approach is demonstrated.
