98629-84-6 Usage
General Description
Tetrahydro-2,4,6-trioxo-1(2H)-pyrimidineacetic acid ethyl ester is a chemical compound with potential applications in the pharmaceutical and agricultural industries. It is an ethyl ester derivative of pyrimidineacetic acid, which is a precursor in the synthesis of various drugs and herbicides. The compound has a unique molecular structure, consisting of a pyrimidine ring with three carbonyl groups and a tetrahydrofuran ring. Its versatile chemical properties make it a promising candidate for the development of new drugs or agrochemicals. Further research and development are essential to explore the full potential and possible applications of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 98629-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,6,2 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 98629-84:
(7*9)+(6*8)+(5*6)+(4*2)+(3*9)+(2*8)+(1*4)=196
196 % 10 = 6
So 98629-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O5/c1-2-15-7(13)4-10-6(12)3-5(11)9-8(10)14/h2-4H2,1H3,(H,9,11,14)
98629-84-6Relevant articles and documents
ALKYLATION OF 6-METHOXYURACIL AND A NEW METHOD FOR THE SYNTHESIS OF N-SUBSTITUTED BARBITURIC ACIDS
Krasnov, K. A.,Slesarev, V. I.,Selimanova, I. N.
, p. 1215 - 1220 (2007/10/02)
The alkylation of the metallic salts of 6-methoxyuracil by dimethyl sulfate and alkyl halides leads to the selective formation of 1-alkyl-6-methoxyuracils.The alkylation of these compounds leads to the formation of 1,3-substituted derivatives of 6-methoxyuracil.The acid hydrolysis of 6-methoxyuracils makes it possible to obtain 1- and 1,3-substituted barbituric acids.
