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)-

(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

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

Formula: C₂₈H₃₇N₅O₁₀S₂

Purity: HP≥98%

Molecular weight: 667.75

Ref: 54-OR1127328

(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

CAS: 105889-80-3

Formula: C₂₈H₃₇N₅O₁₀S₂

Purity: 98%

Molecular weight: 667.7509

Ref: IN-DA0096WH

Cefcapene Impurity 28

CAS: 105889-80-3

Formula: C₂₈H₃₇N₅O₁₀S₂

Molecular weight: 667.75

Ref: 4Z-C-104035

(tert-Butoxycarbonyl)oxycefcapene pivoxil

CAS: 105889-80-3

(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.

Formula: C₂₈H₃₇N₅O₁₀S₂

Purity: Min. 95%

Molecular weight: 667.8 g/mol

Ref: 3D-FEA88980