(S)-tert-Butyl 3-((S)-1-hydroxyethyl)morpholine-4-carboxylate

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Reagent Code: #38373
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CAS Number 1821776-37-7

science Other reagents with same CAS 1821776-37-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.2887 g/mol
Formula C₁₁H₂₁NO₄
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MDL Number MFCD26792479
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This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various drugs, particularly those targeting neurological and cardiovascular conditions. Its chiral structure makes it valuable for producing enantiomerically pure compounds, which are crucial for ensuring the efficacy and safety of medications. Additionally, it is employed in the development of active pharmaceutical ingredients (APIs) that require precise stereochemistry for optimal biological activity. Its application extends to research and development, where it serves as a building block for novel therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,063.00

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(S)-tert-Butyl 3-((S)-1-hydroxyethyl)morpholine-4-carboxylate
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This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various drugs, particularly those targeting neurological and cardiovascular conditions. Its chiral structure makes it valuable for producing enantiomerically pure compounds, which are crucial for ensuring the efficacy and safety of medications. Additionally, it is employed in the development of active pharmaceutical ingredients (APIs) that require precise stereochemistry for optimal biological act

This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various drugs, particularly those targeting neurological and cardiovascular conditions. Its chiral structure makes it valuable for producing enantiomerically pure compounds, which are crucial for ensuring the efficacy and safety of medications. Additionally, it is employed in the development of active pharmaceutical ingredients (APIs) that require precise stereochemistry for optimal biological activity. Its application extends to research and development, where it serves as a building block for novel therapeutic agents.

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