75822-14-9 Usage
General Description
[Nitroso(3-phenylpropyl)amino]acetic acid is a chemical compound that is composed of a nitroso (NO) group, a 3-phenylpropyl amino group, and an acetic acid group. It is a synthetic compound and is not naturally occurring in nature. The presence of the nitroso group makes it a potential precursor to N-nitroso compounds, which are known to be carcinogenic. The 3-phenylpropyl amino group and the acetic acid group indicate that the compound is a derivative of both an amine and an organic acid. Its properties and potential uses are not well-documented but it is likely to be of interest to researchers studying the synthesis and properties of organic compounds with potential biological activity.
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 articles and documents
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.
