55271-47-1 Usage
Uses
Used in Medicinal Chemistry:
Pyridazine-4,5-diol is used as a building block in organic synthesis for the development of pharmaceuticals. Its unique structure and functional groups make it a promising candidate for the creation of new therapeutic agents with potential applications in various medical fields.
Used in Antioxidant and Anti-Inflammatory Applications:
Pyridazine-4,5-diol is utilized for its antioxidant properties, which can help protect cells from oxidative stress and damage. Additionally, its anti-inflammatory effects make it a potential agent for the treatment of inflammatory conditions.
Used in Agrochemical Development:
Pyridazine-4,5-diol has been investigated for its potential use in the development of agrochemicals, where it could contribute to the creation of new pesticides or herbicides with improved efficacy and reduced environmental impact.
Used in Material Science:
pyridazine-4,5-diol has also been explored for its potential use in the development of new materials and polymers, where its unique structure and properties could lead to innovative applications in various industries.
Overall, pyridazine-4,5-diol demonstrates promise in a variety of applications, and ongoing research continues to uncover new potential uses for this versatile compound.
Check Digit Verification of cas no
The CAS Registry Mumber 55271-47-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,7 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55271-47:
(7*5)+(6*5)+(5*2)+(4*7)+(3*1)+(2*4)+(1*7)=121
121 % 10 = 1
So 55271-47-1 is a valid CAS Registry Number.
55271-47-1Relevant articles and documents
Synthesis method of 4,5-dihydroxypyridazine
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Paragraph 0026-0028; 0033, (2021/11/27)
The invention belongs to the technical field of synthesis of medical compounds, and particularly discloses a synthesis method of 4,5-dihydroxypyridazine. The preparation method comprises the following steps: by taking 3,4,6-trichloropyridazine as a raw material, reacting the raw material with a sodium hydroxide aqueous solution to obtain a compound 2; then, subjecting the compound 2 to palladium carbon hydrochlorination to remove chlorine to obtain a compound 3; reacting the compound 3 with N-chlorosuccinimide to obtain a compound 4; and reacting the compound 4 with a sodium hydroxide aqueous solution to obtain the final product that is 4,5-dihydroxypyridazine. The method has the advantages of cheap and easily available raw materials, convenience in production and easiness in purification, and can be developed into an industrial production method.
