Ethyl 4-(aminomethyl)benzoate hydrochloride

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Reagent Code: #87453
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CAS Number 6232-12-8

science Other reagents with same CAS 6232-12-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.68 g/mol
Formula C₁₀H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD00859552
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both an ester and an amino group, makes it valuable for creating molecules with potential therapeutic effects, particularly in the design of drugs targeting neurological disorders or pain management. Additionally, it is employed in organic synthesis for constructing complex molecules due to its reactivity and functional group compatibility. Its hydrochloride form enhances stability and solubility, facilitating its use in laboratory settings.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿378.00
inventory 1g
10-20 days ฿927.00
inventory 5g
10-20 days ฿3,051.00

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Ethyl 4-(aminomethyl)benzoate hydrochloride
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Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both an ester and an amino group, makes it valuable for creating molecules with potential therapeutic effects, particularly in the design of drugs targeting neurological disorders or pain management. Additionally, it is employed in organic synthesis for constructing complex molecules due to its reactivity and f

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both an ester and an amino group, makes it valuable for creating molecules with potential therapeutic effects, particularly in the design of drugs targeting neurological disorders or pain management. Additionally, it is employed in organic synthesis for constructing complex molecules due to its reactivity and functional group compatibility. Its hydrochloride form enhances stability and solubility, facilitating its use in laboratory settings.

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