81633-29-6 Usage
General Description
ETHYL 2-AMINO-4-METHYLPYRIMIDINE-5-CARBOXYLATE is a chemical compound with the molecular formula C9H12N4O2. It is a derivative of pyrimidine and contains an ethyl group, an amino group, a methyl group, and a carboxylate group. ETHYL 2-AMINO-4-METHYLPYRIMIDINE-5-CARBOXYLATE is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential biological activities, including antifungal and antibacterial properties.ETHYL 2-AMINO-4-METHYLPYRIMIDINE-5-CARBOXYLATE is a chemical compound with the molecular formula C9H12N4O2. It is a derivative of pyrimidine and contains an ethyl group, an amino group, a methyl group, and a carboxylate group. ETHYL 2-AMINO-4-METHYLPYRIMIDINE-5-CARBOXYLATE is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential biological activities, including antifungal and antibacterial properties.
Check Digit Verification of cas no
The CAS Registry Mumber 81633-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,3 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81633-29:
(7*8)+(6*1)+(5*6)+(4*3)+(3*3)+(2*2)+(1*9)=126
126 % 10 = 6
So 81633-29-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H11N3O2/c1-3-13-7(12)6-4-10-8(9)11-5(6)2/h4H,3H2,1-2H3,(H2,9,10,11)
81633-29-6Relevant articles and documents
cGAS ANTAGONIST COMPOUNDS
-
, (2017/11/06)
Disclosed are novel compounds of Formula (I) that are cGAS antagonists, methods of preparation of the compounds, pharmaceutical compositions comprising the compounds, and their use in medical therapy.
Facile transformation of Biginelli pyrimidin-2(1H)-ones to pyrimidines. In vitro evaluation as inhibitors of Mycobacterium tuberculosis and modulators of cytostatic activity
Singh, Kamaljit,Singh, Kawaljit,Wan, Baojie,Franzblau, Scott,Chibale, Kelly,Balzarini, Jan
experimental part, p. 2290 - 2294 (2011/06/22)
A series of pyrimidine derivatives bearing amine substituents at C-2 position were obtained from Biginelli 3,4-dihydropyrimidin-2(1H)-ones and the effect of structural variation on anti-TB activity against Mycobacterium tuberculosis H37Rv strai
RECYCLIZATION OF 5-CARBETHOXY-4-METHYL-2-MERCAPTO(AMINO, HYDROXY) PYRIMIDINES TO GIVE 5-ACETYL-2-MERCAPTO(AMINO, HYDROXY)-4-HYDROXYPYRIMIDINES
Vartanyan, R. S.,Kazaryan, Zh. V.,Vartanyan, S. A.
, p. 1212 - 1213 (2007/10/02)
Conditions for the selective preparation of 5-carbethoxy-4-methyl-2-substituted pyrimidines or 5-acetyl-4-hydroxy-2-substituted pyrimidines by condensation of ethoxymethyleneacetoacetic ester with 1,3-binucleophiles are proposed.It is shown that under the influence of sodium ethoxide 5-carbethoxy-4-methyl-2-substituted pyrimidines undergo rearrangement to 5-acetyl-4-hydroxy-2-substituted pyrimidines.
