Tert-Butyl 3-Hydroxy-3-Methyl-Piperidine-1-Carboxylate

≥97%

Reagent Code: #241037
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CAS Number 1104083-27-3

science Other reagents with same CAS 1104083-27-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.29 g/mol
Formula C₁₁H₂₁NO₃
badge Registry Numbers
MDL Number MFCD13194152
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of bioactive molecules due to the presence of a protected piperidine ring and a tertiary alcohol group. Commonly employed in medicinal chemistry for building blocks in drug discovery, especially in the design of enzyme inhibitors and receptor modulators. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies. The tert-butyl carbamate (Boc) protection allows for selective functionalization, making it valuable in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,090.00
inventory 25g
10-20 days ฿15,280.00
Tert-Butyl 3-Hydroxy-3-Methyl-Piperidine-1-Carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of bioactive molecules due to the presence of a protected piperidine ring and a tertiary alcohol group. Commonly employed in medicinal chemistry for building blocks in drug discovery, especially in the design of enzyme inhibitors and receptor modulators. Also utilized in the preparation of analogs for structure-activity relationship (S

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of bioactive molecules due to the presence of a protected piperidine ring and a tertiary alcohol group. Commonly employed in medicinal chemistry for building blocks in drug discovery, especially in the design of enzyme inhibitors and receptor modulators. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies. The tert-butyl carbamate (Boc) protection allows for selective functionalization, making it valuable in multi-step organic syntheses.

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