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

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Reagent Code: #37925
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CAS Number 2109874-10-2

science Other reagents with same CAS 2109874-10-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.53 g/mol
Formula C₈H₁₀BrClFN
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MDL Number MFCD24428137
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the pharmaceutical and chemical research sectors as a chiral building block for the synthesis of more complex molecules. Its structure, featuring both bromo and fluoro substituents, makes it a valuable intermediate in the development of biologically active compounds, particularly in the creation of potential drug candidates. The chiral center allows for the exploration of stereospecific interactions, which is crucial in designing drugs with targeted efficacy and reduced side effects. Additionally, it may be employed in the study of enzyme inhibitors or receptor modulators, where the specific arrangement of atoms can influence binding affinity and activity. Its applications are often focused on advancing medicinal chemistry and drug discovery efforts.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿23,868.00
inventory 100mg
10-20 days ฿11,934.00

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(S)-1-(4-Bromo-3-fluorophenyl)ethanamine hydrochloride
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This compound is primarily utilized in the pharmaceutical and chemical research sectors as a chiral building block for the synthesis of more complex molecules. Its structure, featuring both bromo and fluoro substituents, makes it a valuable intermediate in the development of biologically active compounds, particularly in the creation of potential drug candidates. The chiral center allows for the exploration of stereospecific interactions, which is crucial in designing drugs with targeted efficacy and reduced side effects. Additionally, it may be employed in the study of enzyme inhibitors or receptor modulators, where the specific arrangement of atoms can influence binding affinity and activity. Its applications are often focused on advancing medicinal chemistry and drug discovery efforts.
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