121582-64-7 Usage
Uses
Used in Pharmaceutical Industry:
4-HYDROXY-6-OXO-1-[3-(TRIFLUOROMETHYL)PHENYL]-1,6-DIHYDRO-3-PYRIDAZINECARBOXYLIC ACID is used as a pharmaceutical compound for drug development, leveraging its unique structural properties to create new medications with potential therapeutic benefits.
Used in Chemical Synthesis:
In the chemical synthesis industry, 4-HYDROXY-6-OXO-1-[3-(TRIFLUOROMETHYL)PHENYL]-1,6-DIHYDRO-3-PYRIDAZINECARBOXYLIC ACID serves as a key intermediate in the synthesis of various compounds, contributing to the development of novel chemical entities with diverse applications.
Used as a Research Tool in Scientific Studies:
4-HYDROXY-6-OXO-1-[3-(TRIFLUOROMETHYL)PHENYL]-1,6-DIHYDRO-3-PYRIDAZINECARBOXYLIC ACID is utilized as a research tool in biological and chemical studies, enabling scientists to explore its interactions with biological systems and understand its role in various biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 121582-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,5,8 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 121582-64:
(8*1)+(7*2)+(6*1)+(5*5)+(4*8)+(3*2)+(2*6)+(1*4)=107
107 % 10 = 7
So 121582-64-7 is a valid CAS Registry Number.
121582-64-7Relevant academic research and scientific papers
Pyridazinone compound and use thereof
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Paragraph 0068; 0125-0128, (2017/10/13)
The present invention provides a pyridazinone compound of formula (I) and its use as a plant induced-resistance activator. In the formula, R1-R5 are independently selected from: hydrogen, C1-C6 alkyl, C1-C6 alkoxy, halogen, C1-C6 haloalkyl, C1-C6 haloalkoxy, nitro, amino, CN, NCO, NCS, carboxyl, C1-C3 alkoxy formacyl, and C1-C3 amido; X is selected from oxygen, sulfur and nitrogen; R6 is H, optionally substituted C1-C3 alkyl, optionally substituted phenyl, and 5-10 member heteroaryl; and R7 is H, optionally substituted C1-C3 alkyl and optionally substituted phenyl.
Pyridazines with Heteroatom Substituents in Position 3 and 5. 3) 2-Aryl-5-hydroxypyridazin-3(2H)-ones as Potential Herbicides: Synthesis and Some Reactions
Schober, Bernt D.,Megyeri, Gabor,Kappe, Thomas
, p. 169 - 176 (2007/10/02)
The coupling of dimethyl acetonedicarboxylate 1 with a variety of aryldiazonium salts 2a-i produces the hydrazones 3a-i which can be cyclized in boiling dichlorobenzene to yield the pyridazone esters 4a-i, or in sodium hydroxide solution to give the pyrid
