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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

5-Oxa-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid,7-[[[(difluoromethyl)thio]acetyl]amino]-3-[[[1-(2-hydroxyethyl)-1H-tetrazol-5-yl]thio]methyl]-7-methoxy-8-oxo-, (6R,7R)-

OCCn1nnnc1SCC1=C(C(=O)O)N2[C@H](OC1)[C@](C2=O)(OC)NC(=O)CSC(F)F Request for Quotation
Chemical Name: 5-Oxa-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid,7-[[[(difluoromethyl)thio]acetyl]amino]-3-[[[1-(2-hydroxyethyl)-1H-tetrazol-5-yl]thio]methyl]-7-methoxy-8-oxo-, (6R,7R)-
CAS Number: 99665-00-6
Product Number: AG01DQ91(AGN-PC-0W9QAU)
Synonyms:
MDL No:
Molecular Formula: C15H18F2N6O7S2
Molecular Weight: 496.4662264

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Chemical Structure


Flomoxef, also known as flomoxef sodium or FMOX, is a potent antibiotic belonging to the oxacephem group. In chemical synthesis, Flomoxef serves a crucial role as a key intermediate for the production of various pharmaceutical compounds and active ingredients. Its unique structure and functional groups make it a versatile building block for synthesizing complex organic molecules in the pharmaceutical industry. One of the primary applications of Flomoxef in chemical synthesis is its use as a precursor for the synthesis of cephalosporin antibiotics, which are vital for treating bacterial infections. Additionally, Flomoxef can be utilized in the development of novel drug candidates and pharmaceutical formulations due to its favorable reactivity and pharmacological properties. Its ability to selectively target bacterial cell walls and inhibit crucial enzymes makes it an indispensable tool in the synthesis of antimicrobial agents with enhanced efficacy and reduced resistance. With its broad spectrum of applications in chemical synthesis, Flomoxef continues to play a significant role in advancing drug discovery and development efforts.