(1R,3S,4S)-ETHYL 2-AZABICYCLO[2.2.1]HEPTANE-3-CARBOXYLATE HCL

95%

Reagent Code: #232339
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CAS Number 188057-41-2

science Other reagents with same CAS 188057-41-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.68 g/mol
Formula C₉H₁₆ClNO₂
badge Registry Numbers
MDL Number MFCD08460283
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of neuroactive compounds and centrally acting agents. Its rigid bicyclic structure and defined stereochemistry make it valuable for designing drugs targeting the central nervous system, including potential applications in cognitive enhancers, antidepressants, or antiviral agents. The compound is often employed in asymmetric synthesis to introduce structural complexity and improve selectivity in drug candidates. Its ester functionality allows for further chemical modifications, enabling the preparation of amides, acids, or other derivatives critical in medicinal chemistry optimization.

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inventory 100mg
10-20 days ฿51,950.00

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(1R,3S,4S)-ETHYL 2-AZABICYCLO[2.2.1]HEPTANE-3-CARBOXYLATE HCL
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of neuroactive compounds and centrally acting agents. Its rigid bicyclic structure and defined stereochemistry make it valuable for designing drugs targeting the central nervous system, including potential applications in cognitive enhancers, antidepressants, or antiviral agents. The compound is often employed in asymmetric synthesis to introduce structural complexity and improve selectivity in drug candi

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of neuroactive compounds and centrally acting agents. Its rigid bicyclic structure and defined stereochemistry make it valuable for designing drugs targeting the central nervous system, including potential applications in cognitive enhancers, antidepressants, or antiviral agents. The compound is often employed in asymmetric synthesis to introduce structural complexity and improve selectivity in drug candidates. Its ester functionality allows for further chemical modifications, enabling the preparation of amides, acids, or other derivatives critical in medicinal chemistry optimization.

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