40910-99-4 Usage
Uses
Used in Organic Synthesis:
[ethyl(nitroso)amino]acetic acid is utilized as a key intermediate in organic synthesis, taking advantage of its unique reactivity and structural properties to create a variety of organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [ethyl(nitroso)amino]acetic acid serves as a building block for the synthesis of pharmaceuticals. Its potential applications in this area are attributed to the presence of the nitroso group, which may contribute to the development of novel therapeutic agents.
Used in Research:
[ethyl(nitroso)amino]acetic acid is also employed in research settings to study its chemical and biological properties, particularly focusing on the effects and interactions of the nitroso group within the molecule. This research can lead to a better understanding of its potential applications and limitations in various scientific and industrial contexts.
Check Digit Verification of cas no
The CAS Registry Mumber 40910-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,1 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40910-99:
(7*4)+(6*0)+(5*9)+(4*1)+(3*0)+(2*9)+(1*9)=104
104 % 10 = 4
So 40910-99-4 is a valid CAS Registry Number.
40910-99-4Relevant academic research and scientific papers
Photochemistry of N-nitroso-N-alkyl amino acids: a facile oxidative decarboxylation
Chow, Yuan L.,Horning, Douglas P.,Polo, Joel
, p. 2477 - 2483 (2007/10/02)
Several N-alkyl or N-phenyl-N-nitroso α-amino acids were synthesized and were shown to photolytically rearrange to amidoximes with concurrent decarboxylation in solution or solid states without the presence of externally added acids.In contrast, N-nitrosonipecotinic acid, a N-nitroso β-amino acid, as well as N-nitrosopiperidine in the presence of acetic acid were not photolabile.The photolability of N-nitroso α-amino acids was ascribed to the presence of an intramolecular association between the nitrosamino and carboxyl groups through hydrogen bonding.The species having the hydrogen bonding through the nitroso oxygen in the Z-configuration was believed to be photolabile and decomposed to alkylideneimines as the primary product.The mechanism of the oxidative photorearrangement was discussed.
