3-Iodo-1-(trifluoromethyl)bicyclo[1.1.1]pentane

95%

Reagent Code: #200643
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CAS Number 119934-12-2

science Other reagents with same CAS 119934-12-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.01 g/mol
Formula C₆H₆F₃I
badge Registry Numbers
MDL Number MFCD30723932
thermostat Physical Properties
Boiling Point 150.9±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.05±0.1 g/cm3(Predicted)
Storage 2-8°C, preserved from light, dry sealed

description Product Description

Used as a key building block in medicinal chemistry, particularly in the development of novel pharmaceuticals. Its unique strained bicyclic structure enables efficient bioisosteric replacement of phenyl or tert-butyl groups, improving metabolic stability and solubility. The iodo and trifluoromethyl groups allow for further functionalization via cross-coupling reactions and enhance lipophilicity, making it valuable in drug design for CNS targets and other therapeutic areas. Widely applied in fragment-based drug discovery due to its three-dimensional architecture and favorable physicochemical properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,020.00
inventory 250mg
10-20 days ฿18,900.00
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3-Iodo-1-(trifluoromethyl)bicyclo[1.1.1]pentane
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Used as a key building block in medicinal chemistry, particularly in the development of novel pharmaceuticals. Its unique strained bicyclic structure enables efficient bioisosteric replacement of phenyl or tert-butyl groups, improving metabolic stability and solubility. The iodo and trifluoromethyl groups allow for further functionalization via cross-coupling reactions and enhance lipophilicity, making it valuable in drug design for CNS targets and other therapeutic areas. Widely applied in fragment-base

Used as a key building block in medicinal chemistry, particularly in the development of novel pharmaceuticals. Its unique strained bicyclic structure enables efficient bioisosteric replacement of phenyl or tert-butyl groups, improving metabolic stability and solubility. The iodo and trifluoromethyl groups allow for further functionalization via cross-coupling reactions and enhance lipophilicity, making it valuable in drug design for CNS targets and other therapeutic areas. Widely applied in fragment-based drug discovery due to its three-dimensional architecture and favorable physicochemical properties.

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