(1R,5S)-tert-Butyl 6-hydroxy-3-azabicyclo[3.2.0]heptane-3-carboxylate

95%

Reagent Code: #84786
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CAS Number 1552266-34-8

science Other reagents with same CAS 1552266-34-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.28 g/mol
Formula C₁₁H₁₉NO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of beta-lactam antibiotics. Its bicyclic structure makes it a valuable building block for creating complex molecules with potential antibacterial properties. It is also employed in organic chemistry research for studying ring-opening reactions and stereochemical transformations. Additionally, it serves as a precursor in the preparation of chiral compounds, which are crucial in the production of enantiomerically pure drugs. Its stability and reactivity make it a useful reagent in medicinal chemistry for designing and optimizing drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿31,374.00
inventory 250mg
10-20 days ฿51,975.00

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(1R,5S)-tert-Butyl 6-hydroxy-3-azabicyclo[3.2.0]heptane-3-carboxylate
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This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of beta-lactam antibiotics. Its bicyclic structure makes it a valuable building block for creating complex molecules with potential antibacterial properties. It is also employed in organic chemistry research for studying ring-opening reactions and stereochemical transformations. Additionally, it serves as a precursor in the preparation of chiral compounds, which are crucial in the production

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of beta-lactam antibiotics. Its bicyclic structure makes it a valuable building block for creating complex molecules with potential antibacterial properties. It is also employed in organic chemistry research for studying ring-opening reactions and stereochemical transformations. Additionally, it serves as a precursor in the preparation of chiral compounds, which are crucial in the production of enantiomerically pure drugs. Its stability and reactivity make it a useful reagent in medicinal chemistry for designing and optimizing drug candidates.

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