1-(TERT-BUTOXYCARBONYL)-4-(4-CHLOROPHENYL)PIPERIDINE-4-CARBOXYLIC ACID

95%

Reagent Code: #244899
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CAS Number 644981-94-2

science Other reagents with same CAS 644981-94-2

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Weight 339.81 g/mol
Formula C₁₇H₂₂ClNO₄
badge Registry Numbers
MDL Number MFCD05861537
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents featuring a piperidine core. The tert-butoxycarbonyl (Boc) group protects the nitrogen during synthesis, enabling controlled reactions and enhanced specificity in forming chemical bonds. Its 4-(4-chlorophenyl) and 4-carboxylic acid substituents support the creation of bioactive molecules through further functional group transformations. Commonly employed in medicinal chemistry as a building block for receptor modulators targeting neurological disorders, such as pain, depression, and anxiety. Also utilized in research settings for preparing analogs in structure-activity relationship (SAR) studies.

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inventory 250mg
10-20 days ฿21,380.00

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1-(TERT-BUTOXYCARBONYL)-4-(4-CHLOROPHENYL)PIPERIDINE-4-CARBOXYLIC ACID
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents featuring a piperidine core. The tert-butoxycarbonyl (Boc) group protects the nitrogen during synthesis, enabling controlled reactions and enhanced specificity in forming chemical bonds. Its 4-(4-chlorophenyl) and 4-carboxylic acid substituents support the creation of bioactive molecules through further functional group transformations. Commonly employed in medicina

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents featuring a piperidine core. The tert-butoxycarbonyl (Boc) group protects the nitrogen during synthesis, enabling controlled reactions and enhanced specificity in forming chemical bonds. Its 4-(4-chlorophenyl) and 4-carboxylic acid substituents support the creation of bioactive molecules through further functional group transformations. Commonly employed in medicinal chemistry as a building block for receptor modulators targeting neurological disorders, such as pain, depression, and anxiety. Also utilized in research settings for preparing analogs in structure-activity relationship (SAR) studies.

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