54083-02-2 Usage
Uses
Used in Pharmaceutical Industry:
(6R-cis)-3-(acetoxymethyl)-7-amino-7-methoxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid is used as an antibiotic for the treatment of various bacterial infections. Its application is primarily due to its effectiveness in inhibiting bacterial cell wall synthesis, which results in the destruction of the bacteria and the resolution of the infection.
Used in Respiratory Infections:
In the medical field, (6R-cis)-3-(acetoxymethyl)-7-amino-7-methoxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid is used as a therapeutic agent for respiratory infections. Its application is based on its ability to combat bacteria responsible for respiratory illnesses, such as pneumonia and bronchitis.
Used in Skin Infections:
(6R-cis)-3-(acetoxymethyl)-7-amino-7-methoxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid is also used as a treatment for skin infections, such as impetigo and cellulitis. Its application in this context is due to its effectiveness in targeting and eliminating bacteria that cause skin infections.
Used in Urinary Tract Infections:
Furthermore, (6R-cis)-3-(acetoxymethyl)-7-amino-7-methoxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid is utilized as a medication for urinary tract infections. Its application is attributed to its ability to treat bacterial infections in the urinary system, such as cystitis and pyelonephritis, by inhibiting bacterial growth and promoting the healing process.
Check Digit Verification of cas no
The CAS Registry Mumber 54083-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,8 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54083-02:
(7*5)+(6*4)+(5*0)+(4*8)+(3*3)+(2*0)+(1*2)=102
102 % 10 = 2
So 54083-02-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O6S/c1-5(14)19-3-6-4-20-10-11(12,18-2)9(17)13(10)7(6)8(15)16/h10H,3-4,12H2,1-2H3,(H,15,16)
54083-02-2Relevant academic research and scientific papers
An antibacterial drug cefoxitin acid synthesis method (by machine translation)
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Paragraph 0016; 0018; 0019; 0020, (2016/12/01)
The invention discloses an antibacterial drug cefoxitin acid synthesis method, in order to 7-amino cephalosporanic acid as the raw material, the weak alkaline solution for dissolving the same, then adding etherification enzyme to weak alkaline solution, then adding a oxidation reagent, for etherification reaction, after the etherification reaction, leach etherification enzyme ; adding solidification enzyme in the hydrolysis liquid, after hydrolyzing, after adding ethyl acetate to the solution, start dropping 2-thiophene acetazolamide reagent reaction, reaction-end, two animal pen star dripped in to the reaction solution of vinegar acid salt aqueous solution, separating out crystal, to obtain compound I; compound with I ammonia armor oxygen role acidylated reagent, the compound of I 3 introduces Carboxamide methoxy, cefoxitin acid obtained. Mild reaction conditions of this invention, the synthetic process is simple, easy to implement, effectively improve the yield, shorten the production steps, reduce the production cost, improve product purity, reduce energy consumption, reduce waste water production, suitable for large-scale production. (by machine translation)
