1-(3-Chlorophenyl)ethan-1-amine

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Reagent Code: #163029
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CAS Number 24358-43-8

science Other reagents with same CAS 24358-43-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.62 g/mol
Formula C₈H₁₀ClN
badge Registry Numbers
MDL Number MFCD05215231
inventory_2 Storage & Handling
Storage Room temperature, avoid light, and inert gas storage

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of various active ingredients where an aromatic amine functionality is required. Its structure allows for derivatization in drug development, particularly in compounds targeting central nervous system disorders. Also employed in the creation of specialty chemicals and ligands for catalysis. Due to the presence of both amine and chloro-substituted phenyl groups, it is valuable in cross-coupling reactions and building complex molecules in research settings.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,110.00
inventory 1g
10-20 days ฿2,990.00
inventory 5g
10-20 days ฿11,850.00
inventory 25g
10-20 days ฿51,470.00

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1-(3-Chlorophenyl)ethan-1-amine
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of various active ingredients where an aromatic amine functionality is required. Its structure allows for derivatization in drug development, particularly in compounds targeting central nervous system disorders. Also employed in the creation of specialty chemicals and ligands for catalysis. Due to the presence of both amine and chloro-substituted phenyl groups, it is valuable in cross-cou

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of various active ingredients where an aromatic amine functionality is required. Its structure allows for derivatization in drug development, particularly in compounds targeting central nervous system disorders. Also employed in the creation of specialty chemicals and ligands for catalysis. Due to the presence of both amine and chloro-substituted phenyl groups, it is valuable in cross-coupling reactions and building complex molecules in research settings.

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