1-Cyclohexyl-3-iodobicyclo[1.1.1]pentane

95%

Reagent Code: #130458
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CAS Number 271767-63-6

science Other reagents with same CAS 271767-63-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.16 g/mol
Formula C₁₁H₁₇I
thermostat Physical Properties
Boiling Point 273.5±9.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.57±0.1 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used primarily as a building block in medicinal chemistry, this compound enables the incorporation of the bicyclo[1.1.1]pentane (BCP) motif into target molecules. The BCP group serves as a bioisostere for phenyl rings and alkynes, improving pharmacokinetic properties such as metabolic stability and solubility. The iodine atom allows for further functionalization via cross-coupling reactions, making it valuable in drug discovery for creating novel analogs. Its rigid structure also helps in modulating the conformation of drug candidates, enhancing target selectivity and potency.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿10,850.00
100mg
10-20 days ฿17,340.00

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1-Cyclohexyl-3-iodobicyclo[1.1.1]pentane
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Used primarily as a building block in medicinal chemistry, this compound enables the incorporation of the bicyclo[1.1.1]pentane (BCP) motif into target molecules. The BCP group serves as a bioisostere for phenyl rings and alkynes, improving pharmacokinetic properties such as metabolic stability and solubility. The iodine atom allows for further functionalization via cross-coupling reactions, making it valuable in drug discovery for creating novel analogs. Its rigid structure also helps in modulating the

Used primarily as a building block in medicinal chemistry, this compound enables the incorporation of the bicyclo[1.1.1]pentane (BCP) motif into target molecules. The BCP group serves as a bioisostere for phenyl rings and alkynes, improving pharmacokinetic properties such as metabolic stability and solubility. The iodine atom allows for further functionalization via cross-coupling reactions, making it valuable in drug discovery for creating novel analogs. Its rigid structure also helps in modulating the conformation of drug candidates, enhancing target selectivity and potency.

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