75822-14-9 Usage
Uses
Used in Research and Development:
[Nitroso(3-phenylpropyl)amino]acetic acid is used as a research compound for studying the synthesis and properties of organic compounds with potential biological activity. Its unique structure, featuring a nitroso group, a 3-phenylpropyl amino group, and an acetic acid group, makes it a valuable subject for exploring the interactions and reactions with other molecules and biological systems.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [nitroso(3-phenylpropyl)amino]acetic acid may be used as a starting material or intermediate in the synthesis of various drugs and pharmaceutical compounds. Its potential biological activity and the presence of the nitroso group could be exploited to develop new therapeutic agents or improve the efficacy of existing ones.
Used in Chemical Synthesis:
[Nitroso(3-phenylpropyl)amino]acetic acid can be utilized as a building block in the chemical synthesis of various organic compounds. Its versatile structure allows for further functionalization and modification, making it a useful component in the development of new molecules with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 75822-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,2 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 75822-14:
(7*7)+(6*5)+(5*8)+(4*2)+(3*2)+(2*1)+(1*4)=139
139 % 10 = 9
So 75822-14-9 is a valid CAS Registry Number.
75822-14-9Relevant 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.
