77817-12-0 Usage
Uses
Used in Organic Synthesis:
4-Pyrimidinecarboxylic acid, 6-amino-, methyl ester (9CI) is used as a building block in organic synthesis for the creation of more complex organic compounds. Its unique structure and functional groups contribute to the formation of various chemical entities.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-Pyrimidinecarboxylic acid, 6-amino-, methyl ester (9CI) is utilized as a key intermediate in the development of pharmaceuticals. Its presence in the molecular structure can influence the pharmacological properties of the final drug, potentially leading to new therapeutic agents.
Used in Pharmaceutical Development:
4-Pyrimidinecarboxylic acid, 6-amino-, methyl ester (9CI) is employed as a component in the design and synthesis of new pharmaceuticals. Its chemical versatility allows for the exploration of different drug candidates with potential applications in treating various diseases and medical conditions.
Used in Agrochemical Development:
4-Pyrimidinecarboxylicacid,6-amino-,methylester(9CI) also finds use in the agrochemical industry, where it serves as a precursor in the synthesis of agrochemicals. Its incorporation into the molecular structure of these products can enhance their effectiveness in agricultural applications, such as pest control and crop protection.
Overall, 4-Pyrimidinecarboxylic acid, 6-amino-, methyl ester (9CI) is a multifaceted chemical entity with broad applications across various industries, primarily due to its unique structural features and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 77817-12-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,8,1 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77817-12:
(7*7)+(6*7)+(5*8)+(4*1)+(3*7)+(2*1)+(1*2)=160
160 % 10 = 0
So 77817-12-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N3O2/c1-11-6(10)4-2-5(7)9-3-8-4/h2-3H,1H3,(H2,7,8,9)
77817-12-0Relevant academic research and scientific papers
AZABENZOTHIAZOLE COMPOUNDS, COMPOSITIONS AND METHODS OF USE
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Page/Page column 113, (2012/04/04)
Provided are compounds of Formula I, stereoisomers, tautomers, solvates, prodrugs and pharmaceutically acceptable salts thereof, wherein A, X, R1, R2, R4 and R5 are defined herein, a pharmaceutical composition that includes a compound of Formula I and a pharmaceutically acceptable carrier, adjuvant or vehicle, methods of using the compound or composition in therapy, and methods of 5 manufacturing a compound of Formula I
EQUILIBRIUM NH ACIDITY OF SUBSTITUTED AMINOPYRIMIDINES
Shkurko, O. P.,Terekhova, M. I.,Petrov, E. S.,Mamaev, V. P.,Shatenshtein, A. I.
, p. 260 - 265 (2007/10/02)
The equilibrium NH acidity of 2-, 4-, and 5-aminopyrimidines and their derivatives in dimethyl sulfoxide solution was determined by a transmetallation method.The acidifying effects of the azo groups were estimated by comparison of the obtained pK values of aminopyrimidines and the pK value of aniline and decrease in the order 4-aza >> 2-aza > 3-aza.It was shown that there is a good correlation between the pK values and the relative chemical shifts of the protons of the amino group in the PMR spectra of the aminopyrimidines.Correlation equations relating the pK values of substituted aminopyrimidines to the induction and conjugation constants of the substituents were obtained.
