(4-Oxo-4-Phenyl-Butyl)-Carbamic Acid Tert-Butyl Ester

≥98%

Reagent Code: #221581
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CAS Number 116437-41-3

science Other reagents with same CAS 116437-41-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.33 g/mol
Formula C₁₅H₂₁NO₃
thermostat Physical Properties
Melting Point 90-91 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a protected amine derivative, allowing selective reactions at other functional sites in multi-step syntheses. Commonly employed in the development of bioactive molecules, including enzyme inhibitors and central nervous system agents, due to its stability and ease of deprotection under mild acidic conditions. Also utilized in the construction of peptidomimetics and other nitrogen-containing heterocycles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿440.00
inventory 250mg
10-20 days ฿730.00
inventory 1g
10-20 days ฿2,200.00

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(4-Oxo-4-Phenyl-Butyl)-Carbamic Acid Tert-Butyl Ester
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a protected amine derivative, allowing selective reactions at other functional sites in multi-step syntheses. Commonly employed in the development of bioactive molecules, including enzyme inhibitors and central nervous system agents, due to its stability and ease of deprotection under mild acidic conditions. Also utilized in the construction of peptidomimetics and other nitrogen-contain

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It serves as a protected amine derivative, allowing selective reactions at other functional sites in multi-step syntheses. Commonly employed in the development of bioactive molecules, including enzyme inhibitors and central nervous system agents, due to its stability and ease of deprotection under mild acidic conditions. Also utilized in the construction of peptidomimetics and other nitrogen-containing heterocycles.

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