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123054-30-8

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  • (7R)-7-[(phenylacetyl)amino]-3-trifluoromethanesulfonyloxy-3-cephem-4-carboxylate, 4-methoxybenzyl ester

    Cas No: 123054-30-8

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123054-30-8 Usage

General Description

"(7R)-7-[(phenylacetyl)amino]-3-trifluoromethanesulfonyloxy-3-cephem-4-carboxylate, 4-methoxybenzyl ester" is a complex chemical compound that belongs to the cephalosporin class of antibiotics. It is a derivative of cefpodoxime, a third-generation cephalosporin antibiotic, and contains a phenylacetyl group, a trifluoromethanesulfonyloxy group, and a 4-methoxybenzyl ester. (7R)-7-[(phenylacetyl)amino]-3-trifluoromethanesulfonyloxy-3-cephem-4-carboxylate, 4-methoxybenzyl ester is synthetically produced for its potent antimicrobial properties, particularly in the treatment of bacterial infections. It works by inhibiting the synthesis of bacterial cell walls, leading to the destruction of the microorganisms. Overall, "(7R)-7-[(phenylacetyl)amino]-3-trifluoromethanesulfonyloxy-3-cephem-4-carboxylate, 4-methoxybenzyl ester" is a valuable antibiotic with a broad spectrum of activity against various bacterial pathogens.

Check Digit Verification of cas no

The CAS Registry Mumber 123054-30-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,0,5 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 123054-30:
(8*1)+(7*2)+(6*3)+(5*0)+(4*5)+(3*4)+(2*3)+(1*0)=78
78 % 10 = 8
So 123054-30-8 is a valid CAS Registry Number.

123054-30-8Relevant articles and documents

Studies on anti-MRSA parenteral cephalosporins. III. Synthesis and antibacterial activity of 7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2(Z)- alkoxyimininoacetamido]-3-[(E)-2-(1-alkylimidazol{1,2-b]pyridazinium-6-y) thiovinyl]-3-cephem-4-carboxylates and relat

Ishikawa,Kamiyama,Nakayama,Iizawa,Okonogi,Miyake

, p. 257 - 277 (2007/10/03)

In the course of our exploration for a novel cephalosporin derivative having excellent antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA), we modified the C-3 linked spacers of cephem derivatives bearing a 1-methylimidazo[1,

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