100814-60-6 Usage
Heterocyclical organic compound
The compound has a ring structure in its molecular formula, which includes atoms of different elements (heteroatoms) such as nitrogen and oxygen.
Pyrimidine ring structure
The compound features a pyrimidine ring, which is a six-membered aromatic ring containing four carbon atoms and two nitrogen atoms.
Fluorine atom at the 5-position
A fluorine atom is attached to the pyrimidine ring at the 5th position, which can influence the compound's reactivity, polarity, and lipophilicity.
Potential biological activity
Due to its unique structure and substituents, 2(1H)-Pyrimidinone,4-amino-5-fluoro-5,6-dihydro-6-hydroxy-,trans-(9CI) may exhibit biological activity, making it a potential candidate for further research in drug development or other applications.
Pharmaceutical applications
The compound's structure and properties may make it suitable for use in pharmaceuticals, either as an active ingredient or as a building block for more complex molecules. Further research is needed to explore these possibilities.
Check Digit Verification of cas no
The CAS Registry Mumber 100814-60-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,1 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100814-60:
(8*1)+(7*0)+(6*0)+(5*8)+(4*1)+(3*4)+(2*6)+(1*0)=76
76 % 10 = 6
So 100814-60-6 is a valid CAS Registry Number.
100814-60-6Relevant articles and documents
Glorination of Pyrimidines. Part 2. Mechanistic Aspects of the Reaction of Acetyl Hypofluorite with Uracil and Cytosine Derivatives
Visser, W. M. Gerard,Herder, E. Renella,Kanter, Frans J. J. de,Herscheid D. M. Jacobus
, p. 1203 - 1208 (2007/10/02)
The reaction of acetyl hypofluorite (AcOF) with uracil, cytosine, and some N-1-substituted derivatives dissolved in either acetic acid or water has been investigated.Analysis by radio-h.p.l.c., using (18)f as a tracer, and by (1)H n.m.r. revealed that a substituent at N-1 of uracil has a remarkable effect on the stability of the intermediate 6-acetoxy-5-fluoro-5,6-dihydrouracils.In addition, it was found that these cytosine adducts rapidly deaminate in water yielding their corresponding uracil analogues.
