(2R)-2-((Z)-2-(2-Aminothiazol-4-yl)-2-(hydroxyimino)acetamido)2-((2RS,5RS)-5-methyl-7-oxo-2,4,5,7-tetrahydro-1H-furo(3,4-d)(1,3)thiazin-2-yl)acetic acid

95%

Reagent Code: #229033
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CAS Number 178422-42-9

science Other reagents with same CAS 178422-42-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 413.4 g/mol
Formula C₁₄H₁₅N₅O₆S₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound serves as a key intermediate in the synthesis of cephalosporin antibiotics, particularly in producing broad-spectrum antimicrobials effective against both Gram-negative and Gram-positive bacteria. It enhances the stability of the drug structure against beta-lactamase degradation, leading to improved antibacterial efficacy and prolonged presence in the body. It is suitable for treating infections in the respiratory tract, urinary tract, and bloodstream. Typically employed in the final synthesis stages to yield products with high biological activity and patient safety.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿20,920.00

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(2R)-2-((Z)-2-(2-Aminothiazol-4-yl)-2-(hydroxyimino)acetamido)2-((2RS,5RS)-5-methyl-7-oxo-2,4,5,7-tetrahydro-1H-furo(3,4-d)(1,3)thiazin-2-yl)acetic acid
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This compound serves as a key intermediate in the synthesis of cephalosporin antibiotics, particularly in producing broad-spectrum antimicrobials effective against both Gram-negative and Gram-positive bacteria. It enhances the stability of the drug structure against beta-lactamase degradation, leading to improved antibacterial efficacy and prolonged presence in the body. It is suitable for treating infections in the respiratory tract, urinary tract, and bloodstream. Typically employed in the final synthesis
This compound serves as a key intermediate in the synthesis of cephalosporin antibiotics, particularly in producing broad-spectrum antimicrobials effective against both Gram-negative and Gram-positive bacteria. It enhances the stability of the drug structure against beta-lactamase degradation, leading to improved antibacterial efficacy and prolonged presence in the body. It is suitable for treating infections in the respiratory tract, urinary tract, and bloodstream. Typically employed in the final synthesis stages to yield products with high biological activity and patient safety.
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