(S)-N-Boc-2-morpholinecarbaldehyde

95%

Reagent Code: #236085
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CAS Number 847805-31-6

science Other reagents with same CAS 847805-31-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.25 g/mol
Formula C₁₀H₁₇NO₄
badge Registry Numbers
MDL Number MFCD08752315
thermostat Physical Properties
Boiling Point 309.1 °C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its aldehyde functionality allows for further derivatization through reactions such as reductive amination or Wittig reactions, enabling the construction of complex amine-containing structures. The Boc-protected morpholine ring provides stability and solubility, making it suitable for multi-step organic syntheses, especially in medicinal chemistry for creating protease inhibitors, kinase inhibitors, and other targeted therapies. Commonly employed in asymmetric synthesis due to the preserved stereochemistry, which is critical for the biological activity of final active pharmaceutical ingredients.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,380.00
(S)-N-Boc-2-morpholinecarbaldehyde
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its aldehyde functionality allows for further derivatization through reactions such as reductive amination or Wittig reactions, enabling the construction of complex amine-containing structures. The Boc-protected morpholine ring provides stability and solubility, making it suitable for multi-step organic syntheses, especially in medicinal chemistry for creating p

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its aldehyde functionality allows for further derivatization through reactions such as reductive amination or Wittig reactions, enabling the construction of complex amine-containing structures. The Boc-protected morpholine ring provides stability and solubility, making it suitable for multi-step organic syntheses, especially in medicinal chemistry for creating protease inhibitors, kinase inhibitors, and other targeted therapies. Commonly employed in asymmetric synthesis due to the preserved stereochemistry, which is critical for the biological activity of final active pharmaceutical ingredients.

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