87166-64-1 Usage
Uses
Used in Pharmaceutical Industry:
5-Pyrimidinecarboxaldehyde, 6-amino-1,2,3,4-tetrahydro-2,4-dioxo(9CI) is utilized as an intermediate in the synthesis of pharmaceuticals. Its versatile chemical structure allows for modifications and derivatizations to create a wide range of pharmaceutical products.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Pyrimidinecarboxaldehyde, 6-amino-1,2,3,4-tetrahydro-2,4-dioxo(9CI) serves as a key intermediate in the production of agrochemicals, contributing to the development of new compounds with potential applications in agriculture.
Used in Dye Industry:
5-Pyrimidinecarboxaldehyde, 6-amino-1,2,3,4-tetrahydro-2,4-dioxo(9CI) is also employed in the dye industry, where its unique chemical properties are leveraged to synthesize a variety of dyes with different color characteristics and properties.
Used in Organic Synthesis:
Due to its unique reactivity, 5-Pyrimidinecarboxaldehyde, 6-amino-1,2,3,4-tetrahydro-2,4-dioxo(9CI) is used in organic synthesis for the preparation of various organic compounds, expanding the scope of chemical research and development.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 5-Pyrimidinecarboxaldehyde, 6-amino-1,2,3,4-tetrahydro-2,4-dioxo(9CI) holds potential for the development of new therapeutic agents, given its biological activity and the possibility of creating diverse derivatives with potential medicinal properties.
Check Digit Verification of cas no
The CAS Registry Mumber 87166-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,1,6 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87166-64:
(7*8)+(6*7)+(5*1)+(4*6)+(3*6)+(2*6)+(1*4)=161
161 % 10 = 1
So 87166-64-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H5N3O3/c6-3-2(1-9)4(10)8-5(11)7-3/h1H,(H4,6,7,8,10,11)
87166-64-1Relevant academic research and scientific papers
Synthesis of new pyrimidine derivatives with evaluation of their anti-inflammatory and analgesic activities
Nofal, Zienab M.,Fahmy, Hoda H.,Zarea, Eman S.,El-Eraky, Wafaa
scheme or table, p. 507 - 517 (2012/01/31)
5-Formyl-6-aminopyrimidine-2,4-(1H, 3H)-dione (2) has been previously prepared from compound 1. Cyclocondensation reaction of compound 2 with cyanoacetamide gave substituted pyridopyrimidine 3. Also, compound 2 was condensed with p-amino acetophenone and
SYNTHESIS OF 5-FORMYL-2,4,6-TRISUBSTITUTED PYRIMIDINES
Delia, Thomas J.,Otteman, Ronald
, p. 1805 - 1809 (2007/10/02)
A facile synthesis of 5-formyl-2,4,6-trisubstituted pyrimidines bearing amino and hydroxy groups is described.The Vilsmeier reagent, under mild conditions, gives good yields of products without accompanying chlorination of hydroxy groups.
SYNTHESIS OF PYRIDOPYRIMIDINES ON THE BASIS OF 5-FORMYL-6-AMINOURACILS
Cherdantseva, N. M.,Nesterov, V. M.,Safonova, T. S.
, p. 674 - 677 (2007/10/02)
2,4-Dioxo-1,2,3,4-tetrahydropyridopyrimidines, the structures of which were proved by the PMR and the IR spectra, are formed in the condensation of mono- and di-N-alkyl-5-formyl-6-aminouracils with cyanoacetic acid and its esters, acetoacetic ester
