41867-08-7 Usage
Uses
Used in Chemical Synthesis:
N-Nitroso-N-methyl-DL-phenylalanine is used as an intermediate for the synthesis of sydnone imines, which are a new class of mesoionic compounds. These compounds have potential applications in various fields due to their unique chemical properties.
Used in Pharmaceutical Industry:
N-Nitroso-N-methyl-DL-phenylalanine is used as an intermediate for the production of certain sydnones that are related to natural α-amino acids. These sydnones can be further utilized in the development of pharmaceutical compounds, contributing to the advancement of drug discovery and design.
Used in Research and Development:
In the field of research and development, N-Nitroso-N-methyl-DL-phenylalanine is used as a key compound for studying the properties and reactions of sydnone imines and related compounds. This helps scientists and researchers to better understand the behavior of these compounds and potentially discover new applications or improvements in existing ones.
Used in Organic Chemistry Education:
N-Nitroso-N-methyl-DL-phenylalanine can also be used as a teaching aid in organic chemistry courses, providing students with a practical example of a compound that is involved in the synthesis of mesoionic compounds and other complex organic molecules. This can enhance the learning experience and help students grasp the concepts of organic synthesis and chemical reactions more effectively.
Check Digit Verification of cas no
The CAS Registry Mumber 41867-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,8,6 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 41867-08:
(7*4)+(6*1)+(5*8)+(4*6)+(3*7)+(2*0)+(1*8)=127
127 % 10 = 7
So 41867-08-7 is a valid CAS Registry Number.
41867-08-7Relevant academic research and scientific papers
On the Problem of Regioselectivity in the 1,3-Dipolar Cycloaddition Reaction of Munchnones and Sydnones with Acetylenic Dipolarophiles
Padwa, Albert,Burgess, Edward M.,Gingrich, Henry L.,Roush, David M.
, p. 786 - 791 (2007/10/02)
The 1,3-dipolar cycloaddition reaction of several unsymmetrically substituted munchnones and sydnones with methyl propiolate has been examined.The initially formed cycloadducts readily extrude carbon dioxide to produce five-membered heteroaromatic ring compounds.The reaction of sydnones with methyl propiolate produced a mixture of regioisomeric pyrazoles.The analogous cycloaddition reaction of munchnones with methyl propiolate proceeds with formation of mixtures of both possible regioisomeric pyrroles.The structural assignment of the isolated adducts is based on spectroscopic data.The distribution of products depends on the nature and location of the substituent groups present on the heterocyclic ring.The observed regioselectivity is discussed on the basis of MO-perturbation theory.
