(1R,2S,5S)-rel-3-azabicyclo[3.1.0]hexane-2-carboxylic acid hydrochloride

97%

Reagent Code: #228739
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CAS Number 73836-88-1

science Other reagents with same CAS 73836-88-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.6 g/mol
Formula C₆H₁₀ClNO₂
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MDL Number MFCD20926168
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its rigid bicyclic structure and stereochemistry make it valuable for designing drugs with high selectivity and potency. Commonly employed in medicinal chemistry to improve metabolic stability and binding affinity in drug candidates. Also utilized in the preparation of enzyme inhibitors where precise spatial orientation of functional groups is critical.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,470.00
inventory 500mg
10-20 days ฿34,580.00

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(1R,2S,5S)-rel-3-azabicyclo[3.1.0]hexane-2-carboxylic acid hydrochloride
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Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its rigid bicyclic structure and stereochemistry make it valuable for designing drugs with high selectivity and potency. Commonly employed in medicinal chemistry to improve metabolic stability and binding affinity in drug candidates. Also utilized in the preparation of enzyme inhibitors where precise spatial orientation of functional groups is critical.

Used as a key chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its rigid bicyclic structure and stereochemistry make it valuable for designing drugs with high selectivity and potency. Commonly employed in medicinal chemistry to improve metabolic stability and binding affinity in drug candidates. Also utilized in the preparation of enzyme inhibitors where precise spatial orientation of functional groups is critical.

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