N-(4-Fluorophenyl)-2-hydroxy-N-isopropylacetamide

≥95%

Reagent Code: #220296
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CAS Number 54041-17-7

science Other reagents with same CAS 54041-17-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.23 g/mol
Formula C₁₁H₁₄FNO₂
badge Registry Numbers
MDL Number MFCD11616754
thermostat Physical Properties
Boiling Point 323.8 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. It serves as a building block for beta-adrenergic receptor ligands due to its structural similarity to known adrenergic modulators. Its fluorinated aromatic ring enhances metabolic stability and membrane permeability, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in research settings to study structure-activity relationships in amide-based bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,250.00
inventory 250mg
10-20 days ฿14,010.00
inventory 1g
10-20 days ฿46,400.00

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N-(4-Fluorophenyl)-2-hydroxy-N-isopropylacetamide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. It serves as a building block for beta-adrenergic receptor ligands due to its structural similarity to known adrenergic modulators. Its fluorinated aromatic ring enhances metabolic stability and membrane permeability, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in research settings to study structure-activity relationships in a

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. It serves as a building block for beta-adrenergic receptor ligands due to its structural similarity to known adrenergic modulators. Its fluorinated aromatic ring enhances metabolic stability and membrane permeability, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in research settings to study structure-activity relationships in amide-based bioactive molecules.

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