(S)-1-(3-Bromophenyl)propan-1-amine hydrochloride

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Reagent Code: #37903
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CAS Number 623143-34-0

science Other reagents with same CAS 623143-34-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.56 g/mol
Formula C₉H₁₃BrClN
badge Registry Numbers
MDL Number MFCD12756925
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring a bromophenyl group and an amine functionality, makes it a valuable intermediate in the creation of biologically active compounds. It is often employed in the design and production of drugs targeting the central nervous system, where its chiral nature can influence receptor binding and efficacy. Additionally, it serves as a building block in organic synthesis for the preparation of more complex molecules, including potential therapeutic agents and ligands for asymmetric catalysis. Its applications are particularly relevant in medicinal chemistry, where it aids in the exploration of new drug candidates with improved selectivity and potency.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,950.00
inventory 250mg
10-20 days ฿9,900.00

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(S)-1-(3-Bromophenyl)propan-1-amine hydrochloride
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring a bromophenyl group and an amine functionality, makes it a valuable intermediate in the creation of biologically active compounds. It is often employed in the design and production of drugs targeting the central nervous system, where its chiral nature can influence receptor binding and efficacy. Additionally, it serves as a building block in organic synthesis for the preparation of more complex molecules, including potential therapeutic agents and ligands for asymmetric catalysis. Its applications are particularly relevant in medicinal chemistry, where it aids in the exploration of new drug candidates with improved selectivity and potency.
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