5231-96-9 Usage
Description
2-Acetamidopyridine, with the molecular formula C7H8N2O, is a chemical compound that falls under the category of organic substances known as pyridines and derivatives. It is characterized by its off-white crystalline powder appearance. This versatile compound is utilized as a building block or intermediate in the synthesis of various complex chemical compounds, including dyes, resins, pharmaceuticals, and agrochemicals. Additionally, it serves as an analytical reagent and plays a significant role in metabolic processes, acting as a precursor to numerous enzymes.
Uses
Used in Chemical Synthesis:
2-Acetamidopyridine is used as a building block or intermediate for the production of complex chemical compounds, such as dyes, resins, pharmaceuticals, and agrochemicals. Its presence in these industries is crucial for the synthesis of a wide range of products.
Used in Analytical Chemistry:
As an analytical reagent, 2-Acetamidopyridine is employed in various laboratory settings to facilitate the analysis and identification of different substances. Its role in this field is essential for accurate and reliable results.
Used in Pharmaceutical Industry:
2-Acetamidopyridine is used as a precursor in the development of pharmaceuticals, contributing to the creation of new drugs and medications. Its presence in this industry is vital for the advancement of medical treatments and therapies.
Used in Metabolic Processes:
In biological systems, 2-Acetamidopyridine acts as a precursor to many types of enzymes, playing a crucial role in various metabolic processes. Its function in these processes is essential for maintaining the proper functioning of living organisms.
Check Digit Verification of cas no
The CAS Registry Mumber 5231-96-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,3 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5231-96:
(6*5)+(5*2)+(4*3)+(3*1)+(2*9)+(1*6)=79
79 % 10 = 9
So 5231-96-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O/c1-6(10)9-7-4-2-3-5-8-7/h2-5H,1H3,(H,8,9,10)
5231-96-9Relevant articles and documents
Copper Catalyzed Oxidative C-C Bond Cleavage of 1,2-Diketones: A Divergent Approach to 1,8-Naphthalimides, Biphenyl-2,2′-dicarboxamides, and N-Heterocyclic Amides
Sakhare, Priyanka R.,Subramanian, Parthasarathi,Kaliappan, Krishna P.
, p. 2112 - 2125 (2019/02/14)
We report here a simple and efficient copper catalyzed oxidative C-C bond cleavage of stable aromatic cyclic-fused and acyclic 1,2-diketones to deliver amides and imides in high yields. This newly developed protocol provides an excellent tool to transform structurally different 1,2-diketones into different products under the same reaction conditions. The key synthetic features of this methodology are the formation of 1,8-naphthalimides and biphenyl-2,2′-dicarboxamide motifs in high yields. The fluorescent studies of 1,8-naphthalimide derivatives were also carried out in order to show the potential application of these scaffolds.
A novel three-component reaction of N-fluoropyridinium salts: A facile approach to imidazo[1,2-a]pyridines
Kiselyov, Alexander S.
, p. 4487 - 4490 (2007/10/03)
The reaction of N-fluoropyridinium triflate with isonitriles in acetonitrile and propionitrile in the presence of NaBH(OAc)3 led to the formation of the corresponding imidazo[1,2-a]pyridines in 44-73% yields. The proposed reaction mechanism involves the intermediate formation of a highly reactive carbene species and apparent reduction of the pyridinium intermediate with NaBH(OAc)3 to yield the targeted heterocycles.
Carboxamidation of pyridines by the system of elemental fluorine- carbonitrile-water: A useful alternative to the chichibabin amination
Kiselyov,Strekowski
, p. 2387 - 2392 (2007/10/02)
The title reaction with pyridine, 4-methylpyridine, 3-methylpyridine, 3- bromopyridine, nicotinonitrile, and quinoline yields 2-carboxamido derivatives regioselectively. Isoquinoline is amidated at position 1.
