3-(BOC-AMINOMETHYL)BENZOIC ACID

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Reagent Code: #144657
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CAS Number 117445-22-4

science Other reagents with same CAS 117445-22-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.28 g/mol
Formula C₁₃H₁₇NO₄
badge Registry Numbers
MDL Number MFCD00273426
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and drug candidates. Its structure allows for selective functionalization, making it valuable in constructing complex organic molecules. The BOC-protected amine group enables controlled deprotection during multi-step syntheses, while the carboxylic acid moiety can be readily coupled to amines or alcohols to form amides or esters. Commonly employed in medicinal chemistry for building blocks in protease inhibitors, receptor agonists, and other therapeutic agents. Also utilized in solid-phase synthesis and combinatorial chemistry due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,070.00
inventory 10g
10-20 days ฿4,120.00

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3-(BOC-AMINOMETHYL)BENZOIC ACID
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and drug candidates. Its structure allows for selective functionalization, making it valuable in constructing complex organic molecules. The BOC-protected amine group enables controlled deprotection during multi-step syntheses, while the carboxylic acid moiety can be readily coupled to amines or alcohols to form amides or esters. Commonly employed in medicinal chemistry for buil

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and drug candidates. Its structure allows for selective functionalization, making it valuable in constructing complex organic molecules. The BOC-protected amine group enables controlled deprotection during multi-step syntheses, while the carboxylic acid moiety can be readily coupled to amines or alcohols to form amides or esters. Commonly employed in medicinal chemistry for building blocks in protease inhibitors, receptor agonists, and other therapeutic agents. Also utilized in solid-phase synthesis and combinatorial chemistry due to its stability and reactivity profile.

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