3-Phenylbicyclo[1.1.1]pentane-1-carboxylic acid

95%

Reagent Code: #65996
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CAS Number 83249-04-1

science Other reagents with same CAS 83249-04-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.22 g/mol
Formula C₁₂H₁₂O₂
badge Registry Numbers
MDL Number MFCD00101889
thermostat Physical Properties
Boiling Point 332.9 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a building block for the synthesis of more complex molecules. Its unique bicyclic structure makes it a valuable scaffold in drug discovery, particularly for designing inhibitors and modulators of biological targets. The phenyl group attached to the bicyclo[1.1.1]pentane core enhances its potential to interact with aromatic regions of proteins, improving binding affinity. Researchers often employ it in the development of pharmaceuticals targeting neurological disorders, inflammation, and cancer due to its ability to mimic certain pharmacophores. Additionally, its rigid structure is advantageous in creating compounds with improved metabolic stability and bioavailability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,375.00
inventory 250mg
10-20 days ฿22,500.00
inventory 1g
10-20 days ฿51,300.00

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3-Phenylbicyclo[1.1.1]pentane-1-carboxylic acid
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This compound is primarily utilized in the field of medicinal chemistry as a building block for the synthesis of more complex molecules. Its unique bicyclic structure makes it a valuable scaffold in drug discovery, particularly for designing inhibitors and modulators of biological targets. The phenyl group attached to the bicyclo[1.1.1]pentane core enhances its potential to interact with aromatic regions of proteins, improving binding affinity. Researchers often employ it in the development of pharmaceutica
This compound is primarily utilized in the field of medicinal chemistry as a building block for the synthesis of more complex molecules. Its unique bicyclic structure makes it a valuable scaffold in drug discovery, particularly for designing inhibitors and modulators of biological targets. The phenyl group attached to the bicyclo[1.1.1]pentane core enhances its potential to interact with aromatic regions of proteins, improving binding affinity. Researchers often employ it in the development of pharmaceuticals targeting neurological disorders, inflammation, and cancer due to its ability to mimic certain pharmacophores. Additionally, its rigid structure is advantageous in creating compounds with improved metabolic stability and bioavailability.
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