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CAS 105889-80-3

:

(2,2-Dimethyl-1-oxopropoxy)methyl (6R,7R)-3-[[(aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-thiazolyl]-1-oxo-2-penten-1-yl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

Description:
The chemical substance known as "(2,2-Dimethyl-1-oxopropoxy)methyl (6R,7R)-3-[[[aminocarbonyl]oxy]methyl]-7-[[(2Z)-2-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-thiazolyl]-1-oxo-2-penten-1-yl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate," with the CAS number 105889-80-3, is a complex organic compound characterized by its intricate structure, which includes multiple functional groups such as amides, esters, and thiazoles. This compound is notable for its bicyclic framework, which contributes to its biological activity. It is often studied for its potential pharmacological properties, particularly in the context of antibiotic or antimicrobial applications. The presence of various substituents, including dimethyl and thiazole moieties, suggests that it may interact with biological targets in a specific manner, potentially influencing its efficacy and safety profile. As with many compounds of this nature, its solubility, stability, and reactivity are critical factors that determine its utility in medicinal chemistry and drug development.
Formula:C28H37N5O10S2
InChI:InChI=1S/C28H37N5O10S2/c1-8-9-15(16-12-45-25(30-16)32-26(39)43-28(5,6)7)19(34)31-17-20(35)33-18(14(10-40-24(29)38)11-44-21(17)33)22(36)41-13-42-23(37)27(2,3)4/h9,12,17,21H,8,10-11,13H2,1-7H3,(H2,29,38)(H,31,34)(H,30,32,39)/b15-9-/t17-,21-/m1/s1
InChI key:InChIKey=MBCFXVZYMMCNLY-HDSFYLASSA-N
SMILES:C(OCOC(C(C)(C)C)=O)(=O)C=1N2[C@@]([C@H](NC(/C(=C\CC)/C=3N=C(NC(OC(C)(C)C)=O)SC3)=O)C2=O)(SCC1COC(N)=O)[H]
Synonyms:
  • (2,2-Dimethyl-1-oxopropoxy)methyl (6R,7R)-3-[[(aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-thiazolyl]-1-oxo-2-penten-1-yl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
  • 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[2-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-thiazolyl]-1-oxo-2-pentenyl]amino]-8-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, [6R-[6α,7β(Z)]]-
  • 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-thiazolyl]-1-oxo-2-pentenyl]amino]-8-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, (6R,7R)-
  • 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-[2-[[(1,1-dimethylethoxy)carbonyl]amino]-4-thiazolyl]-1-oxo-2-penten-1-yl]amino]-8-oxo-, (2,2-dimethyl-1-oxopropoxy)methyl ester, (6R,7R)-
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Found 2 products.
  • Cefcapene Impurity 28
    TLC
    + Info

    Cefcapene Impurity 28

    CAS:
    Formula:C28H37N5O10S2
    Molecular weight:667.75

    Ref: 4Z-C-104035

    5mg
    To inquire
    10mg
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    25mg
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    50mg
    To inquire
    100mg
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  • (tert-Butoxycarbonyl)oxycefcapene pivoxil
    Biosynth
    + Info

    (tert-Butoxycarbonyl)oxycefcapene pivoxil

    CAS:
    <p>(Tert-Butoxycarbonyl)oxycefcapene pivoxil is a cephalosporin prodrug, which is a derivative of cephalosporin antibiotics. This compound is synthesized through chemical modification to enhance the pharmacokinetic properties of its parent drug. The mode of action involves the conversion of the prodrug into its active form in vivo, allowing it to effectively inhibit bacterial cell wall synthesis. This action is facilitated by the β-lactam ring, which disrupts the transpeptidation process essential for maintaining bacterial cell wall integrity.</p>
    Formula:C28H37N5O10S2
    Purity:Min. 95%
    Molecular weight:667.8 g/mol

    Ref: 3D-FEA88980

    100mg
    712.00€