Tert-butyl 3-(4-(2-aminoethyl)phenyl)propanoate hydrochloride

≥95%

Reagent Code: #244866
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CAS Number 116856-71-4

science Other reagents with same CAS 116856-71-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.81 g/mol
Formula C₁₅H₂₄ClNO₂
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MDL Number MFCD09997732
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and central nervous system agents. Its structure supports the creation of compounds with neurological activity, including potential antidepressants and neuromodulators. The amine functionality allows for salt formation and further derivatization, enhancing its utility in drug design. The tert-butyl ester serves as a protecting group for the carboxylic acid, enabling selective reactions at the free amine. Commonly employed in research settings for constructing complex organic molecules where a protected carboxylic acid and free amine group are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿47,500.00

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Tert-butyl 3-(4-(2-aminoethyl)phenyl)propanoate hydrochloride
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and central nervous system agents. Its structure supports the creation of compounds with neurological activity, including potential antidepressants and neuromodulators. The amine functionality allows for salt formation and further derivatization, enhancing its utility in drug design. The tert-butyl ester serves as a protecting group for the carboxylic acid, enabling selective reactions at the free

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and central nervous system agents. Its structure supports the creation of compounds with neurological activity, including potential antidepressants and neuromodulators. The amine functionality allows for salt formation and further derivatization, enhancing its utility in drug design. The tert-butyl ester serves as a protecting group for the carboxylic acid, enabling selective reactions at the free amine. Commonly employed in research settings for constructing complex organic molecules where a protected carboxylic acid and free amine group are required.

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