Benzyl(R)-2-methyl-3-oxoazetidine-1-carboxylate

98%

Reagent Code: #155602
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CAS Number 406220-14-2

science Other reagents with same CAS 406220-14-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.24 g/mol
Formula C₁₂H₁₃NO₃
badge Registry Numbers
MDL Number MFCD28501892
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used as an intermediate in the synthesis of β-lactam antibiotics, particularly in the production of carbapenem-class antibiotics which exhibit broad-spectrum antibacterial activity. Its chiral azetidinone core serves as a key building block for constructing the four-membered ring essential for antibiotic efficacy. The benzyl and methyl groups help stabilize the intermediate during multi-step syntheses and can be selectively removed or modified in later stages. Commonly employed in pharmaceutical research and development for creating novel antimicrobial agents with improved resistance profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,080.00
inventory 250mg
10-20 days ฿15,090.00
inventory 500mg
10-20 days ฿20,100.00
inventory 1g
10-20 days ฿26,490.00

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Benzyl(R)-2-methyl-3-oxoazetidine-1-carboxylate
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Used as an intermediate in the synthesis of β-lactam antibiotics, particularly in the production of carbapenem-class antibiotics which exhibit broad-spectrum antibacterial activity. Its chiral azetidinone core serves as a key building block for constructing the four-membered ring essential for antibiotic efficacy. The benzyl and methyl groups help stabilize the intermediate during multi-step syntheses and can be selectively removed or modified in later stages. Commonly employed in pharmaceutical research

Used as an intermediate in the synthesis of β-lactam antibiotics, particularly in the production of carbapenem-class antibiotics which exhibit broad-spectrum antibacterial activity. Its chiral azetidinone core serves as a key building block for constructing the four-membered ring essential for antibiotic efficacy. The benzyl and methyl groups help stabilize the intermediate during multi-step syntheses and can be selectively removed or modified in later stages. Commonly employed in pharmaceutical research and development for creating novel antimicrobial agents with improved resistance profiles.

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