(S)-4-(tert-Butoxycarbonyl)-6,6-dimethylmorpholine-3-carboxylic acid

97%

Reagent Code: #113809
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CAS Number 783349-78-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.30 g/mol
Formula C₁₂H₂₁NO₅
badge Registry Numbers
MDL Number MFCD11053524
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a morpholine ring and a tert-butoxycarbonyl (Boc) protecting group, makes it a valuable intermediate in organic synthesis. It is often employed in the preparation of chiral molecules, where its stereochemistry plays a crucial role in ensuring the desired pharmacological activity. Additionally, it is used in peptide synthesis, where the Boc group protects amine functionalities during the coupling process. Its application extends to medicinal chemistry research, where it aids in the creation of novel drug candidates with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,520.00
inventory 1g
10-20 days ฿28,881.00
inventory 100mg
10-20 days ฿7,056.00
(S)-4-(tert-Butoxycarbonyl)-6,6-dimethylmorpholine-3-carboxylic acid
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a morpholine ring and a tert-butoxycarbonyl (Boc) protecting group, makes it a valuable intermediate in organic synthesis. It is often employed in the preparation of chiral molecules, where its stereochemistry plays a crucial role in ensuring the desired pharmacological activity. Additionally, it is used in peptide synthesis, where the Boc group protects amine functionalities during the coupling process. Its application extends to medicinal chemistry research, where it aids in the creation of novel drug candidates with improved efficacy and selectivity.
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