(R)-1-(3-(1-Aminoethyl)phenyl)-1,1-difluoro-2-methylpropan-2-ol

95%

Reagent Code: #229497
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CAS Number 2738393-85-4

science Other reagents with same CAS 2738393-85-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.27 g/mol
Formula C₁₂H₁₇F₂NO
thermostat Physical Properties
Boiling Point 313.6±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.136±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structural features enable high selectivity and binding affinity to specific enzyme targets, enhancing drug efficacy. The compound's stereochemistry plays a critical role in biological activity, making it valuable in asymmetric synthesis routes for active pharmaceutical ingredients (APIs). It is also employed in research settings to optimize metabolic stability and bioavailability in new drug candidates.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿11,540.00
inventory 100mg
10-20 days ฿19,620.00
inventory 250mg
10-20 days ฿39,230.00

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(R)-1-(3-(1-Aminoethyl)phenyl)-1,1-difluoro-2-methylpropan-2-ol
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structural features enable high selectivity and binding affinity to specific enzyme targets, enhancing drug efficacy. The compound's stereochemistry plays a critical role in biological activity, making it valuable in asymmetric synthesis routes for active pharmaceutical ingredients (APIs). It is also employed in research settings to optimize

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structural features enable high selectivity and binding affinity to specific enzyme targets, enhancing drug efficacy. The compound's stereochemistry plays a critical role in biological activity, making it valuable in asymmetric synthesis routes for active pharmaceutical ingredients (APIs). It is also employed in research settings to optimize metabolic stability and bioavailability in new drug candidates.

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