Tert-Butyl 4-(Dimethylamino)Piperidine-1-Carboxylate

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Reagent Code: #244830
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CAS Number 412293-88-0

science Other reagents with same CAS 412293-88-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.33 g/mol
Formula C₁₂H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD08460150
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require a piperidine backbone with protected functional groups. Its tertiary butyl carbamate (Boc) protection allows for selective deprotection under mild acidic conditions, making it valuable in multi-step organic syntheses. The dimethylamino group enhances solubility and can act as a directing group or participate in salt formation. Commonly employed in the production of central nervous system (CNS) agents, including antipsychotics, antidepressants, and cognitive enhancers, due to the piperidine ring’s prevalence in neuroactive compounds. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿21,810.00

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Tert-Butyl 4-(Dimethylamino)Piperidine-1-Carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require a piperidine backbone with protected functional groups. Its tertiary butyl carbamate (Boc) protection allows for selective deprotection under mild acidic conditions, making it valuable in multi-step organic syntheses. The dimethylamino group enhances solubility and can act as a directing group or participate in salt formation. Commonly employed in the pr

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require a piperidine backbone with protected functional groups. Its tertiary butyl carbamate (Boc) protection allows for selective deprotection under mild acidic conditions, making it valuable in multi-step organic syntheses. The dimethylamino group enhances solubility and can act as a directing group or participate in salt formation. Commonly employed in the production of central nervous system (CNS) agents, including antipsychotics, antidepressants, and cognitive enhancers, due to the piperidine ring’s prevalence in neuroactive compounds. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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