24242-19-1 Usage
Description
5-Aminonicotinic acid, also known as 5-aminopyridine, is an aminonicotinic acid derivative in which the amino group is located at the 5th position of the pyridine ring. It is an aromatic amine, an aminopyridine, and an aminonicotinic acid, with a role as a metabolite. It is functionally related to nicotinic acid and is characterized by its off-white crystalline appearance.
Uses
Used in Chemical Synthesis:
5-Aminonicotinic acid is used as a building block in the synthesis of coordination polymers, which are materials with potential applications in various fields, such as gas storage, catalysis, and drug delivery systems. Its unique chemical structure allows for the formation of complex and diverse structures with interesting properties.
Used in Bioluminescent Reagents:
5-Aminonicotinic acid is utilized as a component in the development of bioluminescent reagents, which are essential tools in the field of biochemistry and molecular biology. These reagents enable the detection and quantification of biological processes, such as gene expression, enzyme activity, and cellular signaling, through the emission of light.
Used in Pharmaceutical Industry:
5-Aminonicotinic acid is employed as a precursor in the synthesis of biologically active agents, which have potential applications in the pharmaceutical industry. These agents can be used for the development of new drugs targeting various diseases and conditions, such as neurological disorders, cardiovascular diseases, and cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 24242-19-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,4 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24242-19:
(7*2)+(6*4)+(5*2)+(4*4)+(3*2)+(2*1)+(1*9)=81
81 % 10 = 1
So 24242-19-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O2/c7-5-1-4(6(9)10)2-8-3-5/h1-3H,7H2,(H,9,10)/p-1
24242-19-1Relevant articles and documents
Efforts toward the synthesis of (+)-Lyconadin A
Karella, Satish,Raghavan, Sadagopan
, (2020/08/10)
Abstract: Synthetic efforts toward the synthesis of (+)-lyconadin A are described. B-Alkyl Suzuki coupling is utilized for combining 2-iodo cyclohexenone with the piperidine subunit. The piperidine subunit is derived from 5-bromo-3-nicotinic acid, and iod
AZOLECARBOXAMIDE HERBICIDES
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Page 46, (2010/02/06)
Compounds of Formula (I), and their N-oxides and agriculturally suitable salts, are disclosed which are useful for controlling undesired vegetation, wherein J is (J-1), (J-2,(J-3), (J-4), (J-5), (J-6), (J-7), (J-8) and R1a, R1b, R1c, R2a, R2b, R3, R4, R05, T, U, W, Y and Z are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula (I) and a method for controlling undesired vegetation which involves contacting the vegetation or its environment with an effective amount of a compound of Formula (I). Also disclosed are mixtures and compositions comprising a herbicidally effective amount of a compound of Formula (Iz) wherein J, R1a, R1b, R1c, R2a, R2b, R3, R4, R05, T, U, W, Y and Z are as defined in the disclosure; and an effective amount of another herbicide or herbicide safener. Also disclosed is a method for selectively controlling undesired vegetation in a crop that involves contacting the locus of a crop with an effective amount of a compound of Formula (Iz) and a effective amount of a safener.
Stereoelectronic substituent effects in polyhydroxylated piperidines and hexahydropyridazines
Jensen, Henrik Helligso,Lyngbye, Laila,Jensen, Astrid,Bols, Mikael
, p. 1218 - 1226 (2007/10/03)
From the pKa values of the conjugate acids of a large series of hydroxylated piperidines and hexahydropyridazines, a consistent difference in basicity was found between stereo-isomers having an axial or equatorial hydroxyl (OH) group either β o
