7229-00-7 Usage
Uses
Used in Medicinal Chemistry:
6-Hydrazino[1,2,4]triazolo[4,3-b]pyridazine is used as a building block for the synthesis of bioactive molecules due to its unique structure and reactivity. It contributes to the development of new drugs or pharmaceutical products.
Used in Drug Development:
In the field of drug development, 6-Hydrazino[1,2,4]triazolo[4,3-b]pyridazine is utilized for its potential to create new therapeutic agents. Its properties may be harnessed to address various medical conditions, pending further research and development.
Used in Materials Science:
6-Hydrazino[1,2,4]triazolo[4,3-b]pyridazine may also find applications in materials science, where its structural and chemical characteristics could be employed to engineer novel materials with specific properties.
Used in Biological Research:
6-Hydrazino[1,2,4]triazolo[4,3-b]pyridazine's potential extends to biological research, where it could be studied for interactions with biological systems, potentially leading to insights in various biological processes and mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 7229-00-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,2 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7229-00:
(6*7)+(5*2)+(4*2)+(3*9)+(2*0)+(1*0)=87
87 % 10 = 7
So 7229-00-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N6/c6-8-4-1-2-5-9-7-3-11(5)10-4/h1-3H,6H2,(H,8,10)
7229-00-7Relevant academic research and scientific papers
Reactivity of triazolo- and tetrazolopyridazines
Katrusiak,Baloniak,Katrusiak
, p. 1279 - 1289 (2007/10/03)
Azolopyridazine derivatives obtained in the reactions of 3-chloro-6-hydrazinopyridazine with formic acid, acetic acid, and nitrous acid are described. By treating triazolo- and tetrazolopyridazines with hydrazine or morpholine, corresponding derivatives s
Synthesis and Reactivity of some 1,2,4-Triazolopyridazine Derivatives
Baloniak, S.,Katrusiak, A.
, p. 683 - 692 (2007/10/02)
The triazolopyridazine derivatives were obtained in the reaction of 3-chloro-6-hydrazinopyridazine with acetic acid and ethyl chloroformate.Acting on 6-chloro-3-methyl-1,2,4-triazolopyridazine with phosphorus pentachloride, a methyl group in position 3 has unexpectedly been exchanged by chlorine.The mechanism of fusing the triazole ring to the pyridazine system has been studied by the reaction of 3-chloro-6-hydrazinopyridazine with formaldehyde, acetaldehyde, and treatment the resulting Schiff bases by bromine in acetic acid with sodium acetate added.Key words: 1,2,4-Triazolopyridazines, nucleophilic substitution, cyclization mechanism
