5663-61-6 Usage
Description
Benzeneacetamide, N-(2-oxoethyl)-, also known as N-(2-acetylphenyl) acetamide, is a white crystalline solid belonging to the class of benzene derivatives. It has a slightly sweet odor and is commonly used as an intermediate in the production of pharmaceuticals and other organic compounds. Additionally, it serves as a flavoring agent in the food industry. However, it is considered a hazardous chemical and should be handled with care due to its potential health and environmental risks.
Uses
Used in Pharmaceutical Industry:
Benzeneacetamide, N-(2-oxoethyl)is used as an intermediate in the production of various pharmaceuticals. Its chemical structure allows it to be a key component in the synthesis of different medicinal compounds, contributing to the development of new drugs and therapies.
Used in Flavoring Agent Applications:
In the food industry, Benzeneacetamide, N-(2-oxoethyl)is employed as a flavoring agent. Its slightly sweet odor makes it suitable for enhancing the taste and aroma of various food products, providing a pleasant sensory experience for consumers.
Used in Organic Compounds Production:
Benzeneacetamide, N-(2-oxoethyl)is also utilized as an intermediate in the production of other organic compounds. Its versatile chemical properties enable it to be a part of the synthesis process for a wide range of organic substances, expanding its applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5663-61-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5663-61:
(6*5)+(5*6)+(4*6)+(3*3)+(2*6)+(1*1)=106
106 % 10 = 6
So 5663-61-6 is a valid CAS Registry Number.
5663-61-6Relevant articles and documents
Design, synthesis, and evaluation of α-ketoheterocycles as class C β-lactamase inhibitors
Kumar, Sanjai,Pearson, Andre L.,Pratt
, p. 2035 - 2044 (2007/10/03)
A series of specific α-ketoheterocycles (benzoxazole, thiazole, imidazole, tetrazole, and thiazole-4-carboxylate) has been synthesized in order to assess their potential as β-lactamase inhibitors. The syntheses were achieved either by construction of the heterocycle (benzoxazole) from an appropriate α-hydroxyimidate, followed by oxidation of the alcohol, or by direct reaction of methyl phenaceturate with a lithiated heterocycle. The properties of these compounds in aqueous solution are described and their inhibitory activity against β-lactamases assessed. They did inhibit the class C β-lactamase of Enterobacter cloacae P99 but not the TEM β-lactamase. The most effective inhibitor of the former enzyme (Ki = 0.11 mM) was 5-(phenylacetylglycyl) tetrazole, probably because it is an anion at neutral pH. Interpretation of the results was aided by computational models of the tetrahedral adducts. Most of the compounds also inhibited α-chymotrypsin but not porcine pancreatic elastase.