(S)-tert-Butyl (5-benzyl-5-azaspiro[2.4]heptan-7-yl)carbamate

98%

Reagent Code: #37131
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CAS Number 144282-37-1

science Other reagents with same CAS 144282-37-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.42 g/mol
Formula C₁₈H₂₆N₂O₂
badge Registry Numbers
MDL Number MFCD17214772
thermostat Physical Properties
Boiling Point 420.48°C
inventory_2 Storage & Handling
Density 1.129g/mL
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a spirocyclic ring system, is particularly valuable in the development of pharmaceutical agents targeting the central nervous system. It is often employed in the preparation of compounds with potential therapeutic effects on neurological disorders, such as anxiety, depression, and neurodegenerative diseases. Additionally, its tert-butyl carbamate group serves as a protective moiety during synthetic processes, enabling selective reactions and enhancing the stability of the intermediate. Its application extends to drug discovery programs where it aids in the optimization of pharmacokinetic properties and biological activity of lead compounds.

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Test Parameter Specification
Appearance White to off-white solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,860.00
inventory 250mg
10-20 days ฿1,520.00

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(S)-tert-Butyl (5-benzyl-5-azaspiro[2.4]heptan-7-yl)carbamate
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a spirocyclic ring system, is particularly valuable in the development of pharmaceutical agents targeting the central nervous system. It is often employed in the preparation of compounds with potential therapeutic effects on neurological disorders, such as anxiety, depression, and neurodegenerative diseases. Additionally, its tert-butyl carbamate group serves as a protective moiety during synthetic processes, enabling selective reactions and enhancing the stability of the intermediate. Its application extends to drug discovery programs where it aids in the optimization of pharmacokinetic properties and biological activity of lead compounds.
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