16014-63-4 Usage
General Description
2-amino-2-carbamimidoyl-acetamide is a chemical compound with the molecular formula C3H8N4O2. It is an organic derivative of urea and has the structural formula H2N-C(=NH)-NHC(=O)CH3. 2-amino-2-carbamimidoyl-acetamide is commonly used in research and laboratory settings as a reagent for the synthesis of various organic compounds. It has also been studied for its potential pharmacological properties, particularly in the field of medicinal chemistry. 2-amino-2-carbamimidoyl-acetamide has also been investigated for its potential use in the treatment of certain medical conditions, although further research is still needed to fully understand its therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 16014-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,1 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16014-63:
(7*1)+(6*6)+(5*0)+(4*1)+(3*4)+(2*6)+(1*3)=74
74 % 10 = 4
So 16014-63-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H8N4O/c4-1(2(5)6)3(7)8/h1H,4H2,(H3,5,6)(H2,7,8)
16014-63-4Relevant articles and documents
Xanthine oxidase (XO): Relative configuration of complexes formed by the enzyme, 2- or 8-N-alkylhypoxanthines and 2-N-alkyl-8-azahypoxanthines. XII
Biagi,Giorgi,Livi,Scartoni,Tonetti,Lucacchini
, p. 357 - 374 (2007/10/02)
Several 2- or 8-n-alkyl-hypoxanthines and a 2,8-di-n-pentylhypoxanthine were synthesized and tested as substrates or inhibitors of Xanthine Oxidase (XO). 8-Alkyl derivatives showed a substrate behaviour, whereas 2-alkyl substituted compounds were non-substrates and inhibitors. 2,8-di-n-pentylhypoxanthine was ineffective as inhibitor. The comparison between their activity allowed us to conclude that the complexes formed by the enzyme and the cited n-alkylhypoxanthines or 2-n -alkyl-8-azahypoxanthines involve their N(3) and N(9) positions in all the cases. The position of the n-alkyl chain determines the disposition of the molecule inside the complex: 2-n-alkyl-hypoxanthines and 2-n-alkyl-8-azahypoxanthines gave complexes with the same orientation of heterocyclic moieties, opposite that given by 8-n-alkyl-hypoxanthines.
