1489-04-9 Usage
Uses
Used in Pharmaceutical Research:
7-Amino-s-triazolo[1,5-a]-s-triazine is utilized as a building block in the synthesis of pharmaceutical compounds, contributing to the development of new drugs. Its unique structure and chemical properties make it a valuable component in medicinal chemistry.
Used in Agrochemical Development:
In the agrochemical industry, 7-Amino-s-triazolo[1,5-a]-s-triazine is employed as a key intermediate in the creation of novel agrochemicals. Its properties allow for the design of compounds with specific pesticidal or herbicidal activities, enhancing crop protection strategies.
Used in Materials Science:
7-Amino-s-triazolo[1,5-a]-s-triazine is also used in materials science for the development of new materials with unique properties. Its structural features and chemical reactivity make it a candidate for creating advanced materials with applications in various industries.
Used in Energetic Materials Research:
Due to its high nitrogen content, 7-Amino-s-triazolo[1,5-a]-s-triazine has been studied for its potential as an energetic component in explosives. Its properties are of interest to researchers looking to develop more efficient and safer explosive materials.
Check Digit Verification of cas no
The CAS Registry Mumber 1489-04-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1489-04:
(6*1)+(5*4)+(4*8)+(3*9)+(2*0)+(1*4)=89
89 % 10 = 9
So 1489-04-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H4N6/c5-3-6-1-7-4-8-2-9-10(3)4/h1-2H,(H2,5,6,7,8,9)
1489-04-9Relevant academic research and scientific papers
A novel multicomponent microwave-assisted synthesis of 5-aza-adenines
Dolzhenko, Anton V.,Kalinina, Svetlana A.,Kalinin, Dmitrii V.
, p. 15850 - 15855 (2013/09/12)
A novel multicomponent strategy for the efficient synthesis of 5-aza-adenines was developed. 5-Aza-adenines were prepared in a one-pot fashion from 5-amino-1,2,4-triazoles, cyanamide and triethyl orthoformate under microwave irradiation. The operational simplicity, efficiency and accessibility of this method make it highly attractive for the generation of bioactive compound libraries.
A new synthesis of amino substituted azolo[1,3,5]triazines via reaction of N1,N1-dimethyl-N2-azolylformamidines with cyanamide
Kalinin, Dmitrii V.,Kalinina, Svetlana A.,Dolzhenko, Anton V.
, p. 147 - 154 (2013/03/13)
The amino substituted triazine ring was annelated to aminoazoles using a new effective synthetic procedure. The method of preparation involved initial formation of azolylformamidines in the reaction of aminoazoles with N,N-dimethylformamide dimethyl acetal followed by the triazine ring closure with cyanamide affording therefore fused aminotriazines.
Reaction of N-Cyanoformimidates with some Heterocyclic Compounds. A New Synthesis of 5-Azaadenine and Related Compounds
Lalezari, I.,Nabahi, S.
, p. 1121 - 1123 (2007/10/02)
3-Amino-1,2,4-triazoles and 2-aminobenzimidazole were reacted with N-cyanoimidates to give 5-amino-1,2,4-triazolo-1,3,5-triazines (5-azaadenines) and 4-aminobenzimidazo-1,3,5-triazines, respectively.The structures of the compounds obtained were confirmed through the comparison with some of the possible isomers prepared by independent methods.
