N-(2-Aminoethyl)-2-chlorobenzamide hydrochloride

95%

Reagent Code: #214680
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CAS Number 94319-83-2

science Other reagents with same CAS 94319-83-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.11 g/mol
Formula C₉H₁₂Cl₂N₂O
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used primarily as an intermediate in the synthesis of bioactive molecules, particularly in pharmaceutical research. It serves as a building block for the preparation of compounds with potential neurological activity, including serotonin and dopamine receptor modulators. Its structure allows for incorporation into more complex molecules where the chlorobenzamide moiety and the aminoethyl side chain contribute to target binding and solubility. Also utilized in the development of novel amide-based derivatives for structure-activity relationship studies. Its hydrochloride salt form enhances stability and handling in synthetic processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,370.00
inventory 1g
10-20 days ฿3,650.00
inventory 5g
10-20 days ฿10,510.00

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N-(2-Aminoethyl)-2-chlorobenzamide hydrochloride
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Used primarily as an intermediate in the synthesis of bioactive molecules, particularly in pharmaceutical research. It serves as a building block for the preparation of compounds with potential neurological activity, including serotonin and dopamine receptor modulators. Its structure allows for incorporation into more complex molecules where the chlorobenzamide moiety and the aminoethyl side chain contribute to target binding and solubility. Also utilized in the development of novel amide-based derivativ

Used primarily as an intermediate in the synthesis of bioactive molecules, particularly in pharmaceutical research. It serves as a building block for the preparation of compounds with potential neurological activity, including serotonin and dopamine receptor modulators. Its structure allows for incorporation into more complex molecules where the chlorobenzamide moiety and the aminoethyl side chain contribute to target binding and solubility. Also utilized in the development of novel amide-based derivatives for structure-activity relationship studies. Its hydrochloride salt form enhances stability and handling in synthetic processes.

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