50681-25-9 Usage
Description
4-Pyridazinecarboxylic acid, also known as the pyridazine analog of Nicotinic Acid, is a chemical compound with significant applications in various fields. It possesses unique properties that make it a valuable compound for research and development.
Uses
Used in Pharmaceutical Industry:
4-Pyridazinecarboxylic acid is used as a glutamate racemase inhibitor for its role in regulating the activity of certain enzymes, which can have implications in the treatment of various neurological disorders.
Used in Research and Development:
4-Pyridazinecarboxylic acid is used as a research compound for the characterization study of nicotinic acid receptors in mouse macrophages, contributing to the understanding of these receptors' functions and their potential applications in medicine.
Used in Surface Electrochemical Studies:
4-Pyridazinecarboxylic acid is used as a subject of study in surface electrochemical research, specifically in the context of its adsorption at Pt(111) surfaces. This research is conducted using electron energy-loss and Auger spectroscopy, providing valuable insights into the compound's interactions with surfaces at the molecular level.
Check Digit Verification of cas no
The CAS Registry Mumber 50681-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,8 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 50681-25:
(7*5)+(6*0)+(5*6)+(4*8)+(3*1)+(2*2)+(1*5)=109
109 % 10 = 9
So 50681-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H16O2/c1-15(16,12-7-4-3-5-8-12)13-9-6-10-14(11-13)17-2/h3-11,16H,1-2H3
50681-25-9Relevant articles and documents
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Heinisch et al.
, p. 799,800, 806 (1976)
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Carboxylation of C-H bonds using N -heterocyclic carbene gold(I) complexes
Boogaerts, Ine I. F.,Nolan, Steven P.
supporting information; experimental part, p. 8858 - 8859 (2010/08/21)
A highly efficient [(NHC)AuI]-based (NHC = N-heterocyclic carbene) catalytic system for the carboxylation of aromatic and heteroaromatic C-H bonds was developed. The significant base strength of the Au-OH species is at the origin of the activation process and permits the facile functionalization of C-H bonds without the use of other organometallic reagents.
Pyridazinone derivatives and processes for preparing the same
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, (2008/06/13)
Disclosed is a pyridazinone compound represented by the formula (I): STR1 wherein X represents hydrogen atom or the like; Y represents a single bonding arm, oxygen atom or sulfur atom; A represents a straight or branched alkylene group which may have a double bond; B represents carbonyl group or thiocarbonyl group; and R2 represents an alkyl group having 1 to 10 carbon atoms which may be substituted or the like; or B represents sulfonyl group; and R2 represents a lower alkenyl group or the like; R1 represents hydrogen atom or the like; R3 represents hydrogen atom or the like; R4 represents hydrogen atom or the like; and R5 represents hydrogen atom or the like, or a pharmaceutically acceptable salt thereof.
Xi:Irritant;
