Methyl 4-Hydroxybicyclo[2.2.2]octane-1-carboxylate

97%

Reagent Code: #172182
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CAS Number 23062-53-5

science Other reagents with same CAS 23062-53-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.23 g/mol
Formula C₁₀H₁₆O₃
badge Registry Numbers
MDL Number MFCD22689519
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. Its rigid bicyclic structure enhances metabolic stability and bioavailability in drug candidates. Commonly employed in the preparation of gamma-aminobutyric acid (GABA) analogs and other neuroactive compounds. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic peptide bonds while resisting enzymatic degradation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,110.00
inventory 250mg
10-20 days ฿11,000.00
inventory 500mg
10-20 days ฿19,960.00
inventory 1g
10-20 days ฿23,480.00
inventory 5g
10-20 days ฿61,780.00

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Methyl 4-Hydroxybicyclo[2.2.2]octane-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. Its rigid bicyclic structure enhances metabolic stability and bioavailability in drug candidates. Commonly employed in the preparation of gamma-aminobutyric acid (GABA) analogs and other neuroactive compounds. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic peptide bonds while resisting enzym

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. Its rigid bicyclic structure enhances metabolic stability and bioavailability in drug candidates. Commonly employed in the preparation of gamma-aminobutyric acid (GABA) analogs and other neuroactive compounds. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to mimic peptide bonds while resisting enzymatic degradation.

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