(S)-tert-Butyl6-(hydroxymethyl)-2,2-dimethylmorpholine-4-carboxylate

97%

Reagent Code: #237702
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CAS Number 1400589-80-1

science Other reagents with same CAS 1400589-80-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.32 g/mol
Formula C₁₂H₂₃NO₄
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MDL Number MFCD22690358
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its protected amine (tert-butyl carbamate) and free hydroxymethyl alcohol functionalities allow for selective modifications in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing complex molecules with high enantiomeric purity. Also utilized in the preparation of bioactive compounds where stereochemistry plays a critical role in biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,990.00
inventory 250mg
10-20 days ฿8,530.00
inventory 1g
10-20 days ฿21,990.00
(S)-tert-Butyl6-(hydroxymethyl)-2,2-dimethylmorpholine-4-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its protected amine (tert-butyl carbamate) and free hydroxymethyl alcohol functionalities allow for selective modifications in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing complex molecules with high enantiomeric purity. Also utilized in the preparation of bioactive compounds where stereochemistry plays a critical ro

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its protected amine (tert-butyl carbamate) and free hydroxymethyl alcohol functionalities allow for selective modifications in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing complex molecules with high enantiomeric purity. Also utilized in the preparation of bioactive compounds where stereochemistry plays a critical role in biological activity.

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