tert-Butyl 4-((1R,2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamido)piperidine-1-carboxylate

98%

Reagent Code: #124255
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CAS Number 1174020-63-3

science Other reagents with same CAS 1174020-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 458.55 g/mol
Formula C₂₄H₃₄N₄O₅
thermostat Physical Properties
Boiling Point 665.9±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.27±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of beta-lactamase inhibitors. These inhibitors play a critical role in combating antibiotic resistance by preventing the breakdown of beta-lactam antibiotics, such as penicillins and cephalosporins, by bacterial enzymes. The compound’s structure, featuring a diazabicyclooctane core, is key to its activity, as it mimics the transition state of the enzyme-substrate interaction, effectively blocking the enzyme’s function. Its application extends to the development of combination therapies, where it is paired with beta-lactam antibiotics to enhance their efficacy against resistant bacterial strains. Additionally, it serves as an intermediate in the production of more complex molecules designed to address multidrug-resistant infections.

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Test Parameter Specification
Appearance Colourless to white to orange solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿98,000.00
inventory 10mg
10-20 days ฿46,800.00

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tert-Butyl 4-((1R,2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxamido)piperidine-1-carboxylate
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of beta-lactamase inhibitors. These inhibitors play a critical role in combating antibiotic resistance by preventing the breakdown of beta-lactam antibiotics, such as penicillins and cephalosporins, by bacterial enzymes. The compound’s structure, featuring a diazabicyclooctane core, is key to its activity, as it mimics the transition state of the enzyme-substrate interaction, effectively blocking

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of beta-lactamase inhibitors. These inhibitors play a critical role in combating antibiotic resistance by preventing the breakdown of beta-lactam antibiotics, such as penicillins and cephalosporins, by bacterial enzymes. The compound’s structure, featuring a diazabicyclooctane core, is key to its activity, as it mimics the transition state of the enzyme-substrate interaction, effectively blocking the enzyme’s function. Its application extends to the development of combination therapies, where it is paired with beta-lactam antibiotics to enhance their efficacy against resistant bacterial strains. Additionally, it serves as an intermediate in the production of more complex molecules designed to address multidrug-resistant infections.

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