40972-16-5 Usage
Uses
Used in Pharmaceutical Industry:
3-Hydrazinopyridazine is used as a pharmaceutical intermediate for its potential role in the development of new drugs. Its unique structure allows for the creation of diverse chemical entities that can target specific biological pathways.
Used in Organic Synthesis:
In the field of organic synthesis, 3-hydrazinopyridazine is utilized as a key building block for the synthesis of heterocyclic compounds, which are important in various chemical and pharmaceutical applications due to their diverse range of biological activities.
Used in Anticancer Research:
3-Hydrazinopyridazine is studied as a potential anti-cancer agent, showing inhibitory effects on the growth of certain cancer cell lines. Its further exploration in this area may lead to the discovery of new therapeutic agents for the treatment of various types of cancer.
While the provided materials do not specify different industries for the uses of 3-Hydrazinopyridazine, the applications mentioned are general and can be applicable across various fields within the chemical and pharmaceutical industries. Further research may reveal additional uses and benefits in other areas.
Check Digit Verification of cas no
The CAS Registry Mumber 40972-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,7 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40972-16:
(7*4)+(6*0)+(5*9)+(4*7)+(3*2)+(2*1)+(1*6)=115
115 % 10 = 5
So 40972-16-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H6N4/c5-7-4-2-1-3-6-8-4/h1-3H,5H2,(H,7,8)
40972-16-5Relevant academic research and scientific papers
Metal free [4+1] and [5+1] annulation reactions to prepare heterocycles using DMF and its derivatives as one-carbon source
Liu, Lingfeng,Qiao, Chunhua,Shen, Bei,Xu, Yiwen
supporting information, (2020/04/01)
1,2,4-Triazolo[3,4-a]pyridines and related heterocycles and substituted triazines were commonly discovered scaffolds in a variety of pharmaceutical and agrochemical agents. Herein, we report a highly efficient and practical method using DMF and its derivative for the [4+1] and [5+1] annulation reactions to prepare these heterocycles. This metal free reaction takes advantages of shelf stable DMF as solvent and carbon donor, imidazole chloride as a catalyst, the mild reaction condition tolerates a broad substrate range and substitutes. The prepared 3-unsubstituted 1,2,4-triazolo[3,4-a]pyridine and derivatives allow further introduction of a variety of functional group1 at 3-position.
Hydrazination of Pyridazines and Phthalazines
Counotte-Potman, A.,Plas, H. C. van der
, p. 1259 - 1261 (2007/10/02)
It is shown by 15N-labelling techniques that hydrazination of pyridazines partly occurs according to a reaction pathway, involving addition of the nucleophile (hydrazine), ring opening and ring closure (SN(ANRORC)-mechanism).It is also proved that phthalazines undergo hydrazination without ring opening (SN(AE)-mechanism).
