5-(Methoxycarbonyl)bicyclo[3.1.1]heptane-1-carboxylic Acid

≥98.0%(qNMR)

Reagent Code: #203697
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CAS Number 110371-28-3

science Other reagents with same CAS 110371-28-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.22 g/mol
Formula C₁₀H₁₄O₄
badge Registry Numbers
MDL Number MFCD00220676
thermostat Physical Properties
Melting Point 82 °C
inventory_2 Storage & Handling
Storage Room temperature

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 makes it valuable for designing bioactive molecules with improved metabolic stability and receptor selectivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing drug candidates for pain management and neurological conditions. Also utilized in the preparation of prodrugs due to the presence of carboxylic acid functional groups that can be modified for enhanced bioavailability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,740.00

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5-(Methoxycarbonyl)bicyclo[3.1.1]heptane-1-carboxylic Acid
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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 makes it valuable for designing bioactive molecules with improved metabolic stability and receptor selectivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing drug candidates for pain management and neurological conditions. Also utilized in the preparation of p

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 makes it valuable for designing bioactive molecules with improved metabolic stability and receptor selectivity. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing drug candidates for pain management and neurological conditions. Also utilized in the preparation of prodrugs due to the presence of carboxylic acid functional groups that can be modified for enhanced bioavailability.

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