4874-33-3 Usage
General Description
5-Pyrimidinol, 2-(methylthio)- (6CI,7CI,8CI,9CI) is a chemical compound that belongs to the pyrimidine family and contains a methylthio group. It is also known by the trade name "USAF EK-6707" and is used in various industrial and research applications. This chemical is commonly utilized as a building block in the synthesis of pharmaceuticals and agrochemicals due to its versatile reactivity and functional groups. Additionally, it has potential biological activity and may be studied for various medicinal and therapeutic purposes. Overall, 5-Pyrimidinol, 2-(methylthio)- (6CI,7CI,8CI,9CI) is a valuable compound with a range of potential applications in the chemical and pharmaceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 4874-33-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4874-33:
(6*4)+(5*8)+(4*7)+(3*4)+(2*3)+(1*3)=113
113 % 10 = 3
So 4874-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2OS/c1-9-5-6-2-4(8)3-7-5/h2-3,8H,1H3
4874-33-3Relevant articles and documents
A mild and general method for the synthesis of 2-substituted-5-hydroxypyrimidines
Medina, Jesus R.,Henry, Theresa A.,Axten, Jeffrey M.
, p. 7363 - 7365 (2006)
5-Bromopyrimidines are converted to 5-hydroxypyrimidines using a mild synthetic procedure. The method is general and can be applied to compounds containing functional groups which are not compatible with the other reagents previously available for this conversion.
SELECTIVE ACID HYDROLYSIS OF 2-SUBSTITUTED-5-DIMETHYLAMINOMETHYLENEAMINOPYRIMIDINES TO 5-AMINO- AND 5-HYDROXYPYRIMIDINES
Kizner, T. A.,Mikhaleva, M. A.,Serebryakova, E. S.
, p. 668 - 670 (2007/10/02)
Conditions are described for the selective acid hydrolysis of 2-substituted-5-dimethylaminomethyleneaminopyrimidines in 0.2-2 M sulfuric acid, to give high yields of the corresponding 5-amino- and difficultly accessible 5-hydroxypyrimidines.
