2073-32-7 Usage
Description
Hexahydro-3-methyl-2H-azepin-2-one, also known as 3-Methylazepan-2-one, is an organic compound with a unique chemical structure that features a seven-membered azepine ring with a methyl group and a ketone functional group. Hexahydro-3-methyl-2H-azepin-2-one is known for its versatile applications in various industries due to its specific chemical properties.
Uses
Used in Pharmaceutical Industry:
Hexahydro-3-methyl-2H-azepin-2-one is used as a key intermediate in the synthesis of RSV (Respiratory Syncytial Virus) inhibitors. These inhibitors play a crucial role in the development of antiviral drugs that help combat respiratory infections caused by the RSV virus.
Used in Polymer Industry:
In the polymer industry, Hexahydro-3-methyl-2H-azepin-2-one is utilized in the preparation of Nylon 6 fibers through caprolactam polymerization. Nylon 6 is a widely used synthetic polymer known for its strength, durability, and resistance to various environmental factors, making it suitable for a range of applications, including textiles, automotive parts, and electrical components.
By understanding the description and uses of Hexahydro-3-methyl-2H-azepin-2-one, we can appreciate its significance in both the pharmaceutical and polymer industries, where it contributes to the development of essential products and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 2073-32-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,7 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2073-32:
(6*2)+(5*0)+(4*7)+(3*3)+(2*3)+(1*2)=57
57 % 10 = 7
So 2073-32-7 is a valid CAS Registry Number.
2073-32-7Relevant articles and documents
Direct and Catalytic Amide Synthesis from Ketones via Transoximation and Beckmann Rearrangement under Mild Conditions
Hyodo, Kengo,Hasegawa, Genna,Oishi, Naoki,Kuroda, Kazuma,Uchida, Kingo
, p. 13080 - 13087 (2018/11/02)
The Br?nsted acid-catalyzed synthesis of secondary amides from ketones under mild conditions is described via transoximation and Beckmann rearrangement using O-protected oximes as more stable equivalents of explosive O-protected hydroxylamines. This methodology could be applied to highly rearrangement-selective amide synthesis from α-branched alkyl aryl ketones and performed on a 1-g scale. The presence of water is essential for this reaction, and its role was clarified by isotope-labeling experiments.
Amidino derivatives useful as nitric oxide synthase inhibitors
-
, (2008/06/13)
The current invention discloses useful pharmaceutical compositions containing amidino derivative useful as nitric oxide synthase inhibitors.
Novel Approach to Lactams via (Triisopropylsilyl)azidohydrin Formation and Photoinduced Schmidt Rearrangement
Evans, P. Andrew,Modi, Dilip P.
, p. 6662 - 6663 (2007/10/03)
-
