6296-86-2 Usage
Pyridazine derivative
A compound based on the pyridazine ring structure This indicates that the compound is derived from the pyridazine ring, which is a six-membered heterocyclic ring with two nitrogen atoms.
4-Methoxyphenyl group
A phenyl group (a six-carbon ring) with a methoxy group (-OCH3) attached to the fourth carbon This describes one of the substituents on the pyridazine ring, which has a methoxy group attached to it.
Methyl group
A single carbon atom with three hydrogen atoms (-CH3) This describes the other substituent on the pyridazine ring, which is a methyl group.
Potential pharmaceutical applications
Possible uses in the development of drugs This highlights the potential for 2-(4-methoxyphenyl)-6-methylpyridazin-3(2H)-one to be used in the pharmaceutical industry.
Medicinal chemistry
Involvement in the field of designing and synthesizing therapeutic agents This indicates that the compound may be relevant in the area of medicinal chemistry, which focuses on creating new drugs.
Drug development
The process of creating new pharmaceuticals for various medical conditions This suggests that 2-(4-methoxyphenyl)-6-methylpyridazin-3(2H)-one could be a candidate for further development as a drug.
Antimicrobial potential
The ability to inhibit or kill microorganisms This indicates that the compound may have properties that could be useful in fighting infections caused by bacteria, fungi, or other microorganisms.
Anticancer potential
The possibility of being used to treat or prevent cancer This suggests that 2-(4-methoxyphenyl)-6-methylpyridazin-3(2H)-one may have properties that could be beneficial in cancer treatment or prevention.
Anti-inflammatory potential
The ability to reduce inflammation in the body This indicates that the compound may have properties that could be useful in treating conditions associated with inflammation, such as arthritis or allergies.
Further research and development
The need for additional studies to investigate and characterize the specific properties and potential uses of the compound This highlights that more work is needed to fully understand the capabilities and applications of 2-(4-methoxyphenyl)-6-methylpyridazin-3(2H)-one.
Check Digit Verification of cas no
The CAS Registry Mumber 6296-86-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6296-86:
(6*6)+(5*2)+(4*9)+(3*6)+(2*8)+(1*6)=122
122 % 10 = 2
So 6296-86-2 is a valid CAS Registry Number.
6296-86-2Relevant academic research and scientific papers
Pu, Yu-Ming,Ku, Yi-Yin,Grieme, Tim,Henry, Rodger,Bhatia, Ashok V.
, p. 149 - 153 (2006)
N-Arylation of pridazinone derivatives 1 with an aryl or heteroaryl bromide or iodide 2 has been achieved in 70-94% isolated yield using catalytic amounts of the stable and structurally well defined copper catalyst 4b under standard Ullmann-Goldberg reaction conditions. The structure of copper catalyst 4b was characterized by ESI-MS, DSC and the single crystal X-ray.
