14704-64-4 Usage
Uses
Used in Pharmaceutical Synthesis:
4-amino-6-chloro-2H-pyridazin-3-one is used as a key intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into various drug molecules, enhancing their therapeutic properties and targeting specific biological pathways.
Used in Agrochemical Production:
In the agrochemical industry, 4-amino-6-chloro-2H-pyridazin-3-one is utilized as a starting material for the development of new pesticides and herbicides, leveraging its chemical structure to improve the effectiveness and selectivity of these compounds in agricultural applications.
Used in Materials Science:
4-amino-6-chloro-2H-pyridazin-3-one may also find potential applications in materials science, where its unique structure and properties could contribute to the development of advanced materials with specific characteristics, such as improved conductivity, stability, or responsiveness to environmental stimuli.
Overall, the diverse applications of 4-amino-6-chloro-2H-pyridazin-3-one across different industries highlight its importance as a versatile chemical compound with significant potential for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 14704-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,0 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14704-64:
(7*1)+(6*4)+(5*7)+(4*0)+(3*4)+(2*6)+(1*4)=94
94 % 10 = 4
So 14704-64-4 is a valid CAS Registry Number.
14704-64-4Relevant academic research and scientific papers
DIRECT AMINATION OF 3(2H)-PYRIDAZINONES: RE-INVESTIGATION OF THE REACTION OF 3,6-DIMETHOXYPYRIDAZINE WITH HYDRAZINE
Coates, William J.,McKillop, Alexander
, p. 1313 - 1329 (2007/10/02)
3,6-Dimethoxypyridazine has been shown to react with hydrazine via 4-amination of 6- methoxy and 6-hydrazino-3(2H)-pyridazinones to give 4-amino-6-methoxy- and 4-amino-6-hydrazino-3(2H)-pyridazinones, and not the corresponding 5-amino isomers as previously reported.The published synthesis of the 5-amino isomers, used to confirm the earlier findings, is incorrect as regards 5-amino-6-hydrazino-3(2H)-pyridazinone, which has been prepared by an alternative route.The 4-aminnation reaction has been extended to 6-chloro-3(2H)-pyridazinone.
