(1R)-1-(4-fluoronaphthyl)ethylamine

95%

Reagent Code: #231160
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CAS Number 1211568-72-7

science Other reagents with same CAS 1211568-72-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.23 g/mol
Formula C₁₂H₁₂FN
badge Registry Numbers
MDL Number MFCD09414754
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and receptor modulators. Its fluorinated aromatic structure enhances binding affinity and metabolic stability in drug candidates. Commonly employed in asymmetric synthesis to introduce chirality due to the presence of a stereogenic center. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays, leveraging the naphthyl group’s intrinsic fluorescence.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,370.00
inventory 250mg
10-20 days ฿19,990.00
inventory 1g
10-20 days ฿54,000.00

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(1R)-1-(4-fluoronaphthyl)ethylamine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and receptor modulators. Its fluorinated aromatic structure enhances binding affinity and metabolic stability in drug candidates. Commonly employed in asymmetric synthesis to introduce chirality due to the presence of a stereogenic center. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays, leveraging the naphthyl group’s in

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and receptor modulators. Its fluorinated aromatic structure enhances binding affinity and metabolic stability in drug candidates. Commonly employed in asymmetric synthesis to introduce chirality due to the presence of a stereogenic center. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays, leveraging the naphthyl group’s intrinsic fluorescence.

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