1-(Tert-Butoxycarbonyl)Hexahydroazepine

95%

Reagent Code: #122376
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CAS Number 123387-52-0

science Other reagents with same CAS 123387-52-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.29 g/mol
Formula C₁₁H₂₁NO₂
badge Registry Numbers
MDL Number MFCD18252672
inventory_2 Storage & Handling
Density 0.967 g/mL at 25 °C
Storage -20°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It is commonly employed in peptide chemistry for the protection of amine groups during complex organic reactions. Its stability and ease of deprotection make it valuable in the production of heterocyclic compounds and bioactive molecules. Additionally, it finds application in the preparation of agrochemicals and fine chemicals, where precise control over molecular structure is essential. Its versatility in organic synthesis contributes to its use in research and industrial-scale manufacturing processes.

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Test Parameter Specification
Appearance Report result
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,854.00
inventory 1g
10-20 days ฿3,699.00
inventory 100mg
10-20 days ฿1,233.00

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1-(Tert-Butoxycarbonyl)Hexahydroazepine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It is commonly employed in peptide chemistry for the protection of amine groups during complex organic reactions. Its stability and ease of deprotection make it valuable in the production of heterocyclic compounds and bioactive molecules. Additionally, it finds application in the preparation of agrochemicals and fine chemicals, where precise control over molecular structure is essential. Its versatility in organic synthesis contributes to its use in research and industrial-scale manufacturing processes.
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