(S)-1-(4-Bromo-3-fluorophenyl)ethanamine

95%

Reagent Code: #236646
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CAS Number 1241678-53-4

science Other reagents with same CAS 1241678-53-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.07 g/mol
Formula C₈H₉BrFN
badge Registry Numbers
MDL Number MFCD07772576
inventory_2 Storage & Handling
Storage Room temperature, avoid light

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure contains both bromo and fluoro substituents, making it valuable for cross-coupling reactions in drug discovery. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in central nervous system agents and anti-inflammatory compounds. The amine functionality allows for easy derivatization, enabling rapid generation of compound libraries for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,530.00
inventory 250mg
10-20 days ฿14,250.00
inventory 1g
10-20 days ฿38,130.00
(S)-1-(4-Bromo-3-fluorophenyl)ethanamine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure contains both bromo and fluoro substituents, making it valuable for cross-coupling reactions in drug discovery. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in central nervous system agents and anti-inflammatory compounds. The amine functionality allows for easy deri

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure contains both bromo and fluoro substituents, making it valuable for cross-coupling reactions in drug discovery. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in central nervous system agents and anti-inflammatory compounds. The amine functionality allows for easy derivatization, enabling rapid generation of compound libraries for structure-activity relationship studies.

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