(R)-1-(3-Fluorophenyl)-N-methylethanamine

97%

Reagent Code: #228667
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CAS Number 1212124-79-2

science Other reagents with same CAS 1212124-79-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.2 g/mol
Formula C₉H₁₂FN
badge Registry Numbers
MDL Number MFCD07779099
thermostat Physical Properties
Boiling Point 178.8±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.004±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its fluorinated aromatic structure and amine functionality make it suitable for drug candidates targeting neurological disorders. The (R)-enantiomer is often preferred for its stereoselective activity in biological systems. It may serve as an intermediate in the production of antidepressants, antipsychotics, or other bioactive molecules where fluorine substitution enhances metabolic stability and binding affinity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,300.00
inventory 1g
10-20 days ฿65,580.00
(R)-1-(3-Fluorophenyl)-N-methylethanamine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its fluorinated aromatic structure and amine functionality make it suitable for drug candidates targeting neurological disorders. The (R)-enantiomer is often preferred for its stereoselective activity in biological systems. It may serve as an intermediate in the production of antidepressants, antipsychotics, or other bioactive molecules where fluorine substitution enhance

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its fluorinated aromatic structure and amine functionality make it suitable for drug candidates targeting neurological disorders. The (R)-enantiomer is often preferred for its stereoselective activity in biological systems. It may serve as an intermediate in the production of antidepressants, antipsychotics, or other bioactive molecules where fluorine substitution enhances metabolic stability and binding affinity.

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