6-O-Methyl-2',4''-bis-O-(trimethylsilyl)-9-[O-(1-ethoxy-1-methylethyl)oxime]-Erythromycin

95%

Reagent Code: #122975
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CAS Number 119665-62-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 993.46 g/mol
Formula C₄₉H₉₆N₂O₁₄Si₂
thermostat Physical Properties
Boiling Point 838.4°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Primarily utilized in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of modified erythromycin derivatives. Its structural modifications enhance stability and bioavailability, making it valuable for studying and developing new macrolide antibiotics. Researchers employ it to explore potential treatments for bacterial infections, particularly those resistant to conventional antibiotics. Additionally, it is used in chemical studies to investigate the relationship between molecular structure and biological activity, aiding in the design of more effective therapeutic agents. Its application is critical in advancing the understanding of macrolide chemistry and improving antibiotic efficacy.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿2,400.00
inventory 1g
10-20 days ฿1,200.00
6-O-Methyl-2',4''-bis-O-(trimethylsilyl)-9-[O-(1-ethoxy-1-methylethyl)oxime]-Erythromycin
Primarily utilized in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of modified erythromycin derivatives. Its structural modifications enhance stability and bioavailability, making it valuable for studying and developing new macrolide antibiotics. Researchers employ it to explore potential treatments for bacterial infections, particularly those resistant to conventional antibiotics. Additionally, it is used in chemical studies to investigate the relationship between molecular structure and biological activity, aiding in the design of more effective therapeutic agents. Its application is critical in advancing the understanding of macrolide chemistry and improving antibiotic efficacy.
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