1416134-44-5 Usage
Description
(x)C2H2O4C20H24N2O3 is a complex chemical compound consisting of two main components: oxalic acid (C2H2O4) and a large organic molecule with the molecular formula C20H24N2O3. Oxalic acid is a strong organic acid found in many plants and vegetables, while the second component is a compound containing carbon, hydrogen, nitrogen, and oxygen atoms. The exact identity and properties of (x)C2H2O4C20H24N2O3 depend on the specific value of "x" and the ratio of the two components. It could be a pharmaceutical drug, a natural product, or a synthetic compound.
Uses
Used in Pharmaceutical Industry:
(x)C2H2O4C20H24N2O3 is used as a pharmaceutical drug for its potential therapeutic applications. (x)C2H2O4C20H24N2O3 may have various biological activities, depending on its specific structure and properties, which can be exploited for the development of new drugs to treat various diseases.
Used in Chemical Industry:
(x)C2H2O4C20H24N2O3 can be used as a raw material or intermediate in the chemical industry for the synthesis of other compounds. (x)C2H2O4C20H24N2O3's unique structure and properties may allow it to be used in the production of various chemicals, materials, or other products.
Used in Research and Development:
(x)C2H2O4C20H24N2O3 may be used as a research compound for studying its properties, interactions, and potential applications. Researchers can investigate the compound's chemical reactivity, stability, and other characteristics to better understand its behavior and potential uses.
Used in Agriculture:
(x)C2H2O4C20H24N2O3 could potentially be used in the agricultural industry, for example, as a component of fertilizers, pesticides, or other agrochemicals. Its specific application would depend on its properties and compatibility with other substances used in agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 1416134-44-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,6,1,3 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1416134-44:
(9*1)+(8*4)+(7*1)+(6*6)+(5*1)+(4*3)+(3*4)+(2*4)+(1*4)=125
125 % 10 = 5
So 1416134-44-5 is a valid CAS Registry Number.
1416134-44-5Relevant articles and documents
Method for synthesizing avibactam intermediate compound
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, (2019/11/20)
The invention relates to a method for synthesizing an avibactam intermediate compound. The specific synthetic route of the method is as described in the specification. According to a technical schemeof the invention, no precious metal catalyst is used, and no heavy metal pollution is produced; high yield and low cost are realized; and the method is mild in reaction condition and friendly to environment, and can realize industrial production.
B-LACTAMASE INHIBITOR AND APPLICATION THEREOF
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, (2018/03/07)
The present invention relates to a compound of Formula (I)-(IV) useful as β-lactamase inhibitor, a pharmaceutically acceptable salt, ester, solvate or stereoisomer thereof, wherein R1, R2, M and ring A have definitions as those in the specification. The present invention further relates to methods for preparing these compounds, pharmaceutical compositions comprising these compounds, and uses of these compounds. For example, the compounds of the present invention can be used as β-lactamase inhibitors, for treatment and/or prophylaxis of diseases caused by bacterial infections, solving drug-resistance problems caused by β-lactamases, especially bacterial drug-resistant diseases caused by type B metallo-β-lactamases.
Development of a Manufacturing Route to Avibactam, a β-Lactamase Inhibitor
Ball, Matthew,Boyd, Alistair,Ensor, Gareth J.,Evans, Matthew,Golden, Michael,Linke, Simon R.,Milne, David,Murphy, Rebecca,Telford, Alex,Kalyan, Yuriy,Lawton, Graham R.,Racha, Saibaba,Ronsheim, Melanie,Zhou, Shao Hong
, p. 1799 - 1805 (2016/10/31)
Process development work to provide an efficient, robust, and cost-effective manufacturing route to avibactam, a β-lactamase inhibitor is presented herewith. Aspects of this optimization work include the counterintuitive introduction of a protecting group to effect a difficult urea formation and the use of controlled feed hydrogenation conditions to facilitate an elegant one pot debenzylation and sulfation reaction. Overall, the commercial process delivers avibactam in much improved yield with significant reduction in the environmental footprint.
