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Sodium (6R,7R)-7-[(2E)-2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate, also known as cefuroxime sodium, is a semisynthetic, broad-spectrum cephalosporin antibiotic. It is characterized by its ability to treat a wide range of bacterial infections and works by inhibiting the formation of the bacteria's cell wall, leading to bacterial cell death.

65243-25-6

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65243-25-6 Usage

Uses

Used in Medical Applications:
Cefuroxime sodium is used as an antibiotic for treating various bacterial infections, such as respiratory, urinary tract, skin, and soft tissue infections. It is effective against a broad spectrum of bacteria, making it a versatile choice for treating different types of infections.
Used in Intravenous or Intramuscular Administration:
Cefuroxime sodium is available as an injectable solution for intravenous or intramuscular administration, allowing for direct delivery into the bloodstream to quickly reach the site of infection.
Used under Medical Supervision:
It is typically prescribed under medical supervision to ensure proper dosage and administration, as well as to monitor for potential side effects and complications.
Used with Caution for Antibiotic Resistance:
As with all antibiotics, it is important to use cefuroxime sodium only as directed by a healthcare professional to minimize the risk of antibiotic resistance and other potential complications. This helps to preserve the effectiveness of the antibiotic for future use.

Check Digit Verification of cas no

The CAS Registry Mumber 65243-25-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,4 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65243-25:
(7*6)+(6*5)+(5*2)+(4*4)+(3*3)+(2*2)+(1*5)=116
116 % 10 = 6
So 65243-25-6 is a valid CAS Registry Number.

65243-25-6Downstream Products

65243-25-6Relevant academic research and scientific papers

IMPROVED PROCESS FOR THE PREPARATION OF CEPHALOSPORIN ANTIBIOTICS

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Page/Page column 9-10, (2008/06/13)

Abstract The present invention more particularly relates to a process for the preparation of cephalosporin antibiotics of the Formula (I) wherein R1 represents hydrogen, trityl, alkyl like CH3, CRaRbCOORc where Ra and Rb independently represent hydrogen or methyl and Rc represents hydrogen or (C1-C6) alkyl; R2 is carboxylate ion or COORd, where Rd represents hydrogen, ester or a counter ion which forms a salt; R3 represents hydrogen, CH3, CH2OCH3, CH2OCOCH3, CH=CH2, Formula (II).

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