(2S,3S)-3-Amino-2-methyl-4-oxoazetidine-1-sulfonic acid

97%

Reagent Code: #113173
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CAS Number 80082-65-1

science Other reagents with same CAS 80082-65-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.18 g/mol
Formula C₄H₈N₂O₄S
badge Registry Numbers
MDL Number MFCD08061571
inventory_2 Storage & Handling
Density 1.75g/cm3
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of beta-lactam antibiotics. Its unique structure, featuring an azetidine ring, makes it valuable for developing antibiotics that target bacterial cell wall synthesis. It is particularly significant in the production of monobactams, a class of antibiotics effective against Gram-negative bacteria. Additionally, its sulfonic acid group enhances its solubility and reactivity, facilitating its incorporation into more complex pharmaceutical compounds. Researchers also explore its potential in designing novel antimicrobial agents to combat drug-resistant bacterial strains.

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Test Parameter Specification
APPEARANCE White to off-white Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿288.00
inventory 10g
10-20 days ฿567.00
inventory 25g
10-20 days ฿1,206.00

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(2S,3S)-3-Amino-2-methyl-4-oxoazetidine-1-sulfonic acid
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of beta-lactam antibiotics. Its unique structure, featuring an azetidine ring, makes it valuable for developing antibiotics that target bacterial cell wall synthesis. It is particularly significant in the production of monobactams, a class of antibiotics effective against Gram-negative bacteria. Additionally, its sulfonic acid group enhances its solubility and reactivity, facilitating its incorp

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of beta-lactam antibiotics. Its unique structure, featuring an azetidine ring, makes it valuable for developing antibiotics that target bacterial cell wall synthesis. It is particularly significant in the production of monobactams, a class of antibiotics effective against Gram-negative bacteria. Additionally, its sulfonic acid group enhances its solubility and reactivity, facilitating its incorporation into more complex pharmaceutical compounds. Researchers also explore its potential in designing novel antimicrobial agents to combat drug-resistant bacterial strains.

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