40910-99-4 Usage
General Description
[ethyl(nitroso)amino]acetic acid is a chemical compound with the molecular formula C4H8N2O4. It is a derivative of amino acids and contains a nitroso group. [ethyl(nitroso)amino]acetic acid is a white solid at room temperature and is soluble in water. It is commonly used in organic synthesis and research due to its unique structure and reactivity. It has potential applications in medicinal chemistry, as well as being used as a building block for the synthesis of other organic compounds. The presence of the nitroso group in [ethyl(nitroso)amino]acetic acid makes it an interesting target for studying its chemical and biological properties.
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 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.
