(S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidine

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Reagent Code: #38376
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CAS Number 207113-36-8

science Other reagents with same CAS 207113-36-8

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Weight 201.3812 g/mol
Formula C₁₀H₂₃NOSi
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MDL Number MFCD09909497
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(S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidine is widely used in organic synthesis, particularly as a chiral building block or intermediate in the production of pharmaceuticals and bioactive compounds. Its silyl-protected hydroxyl group enhances stability and selectivity during complex reactions, making it valuable in asymmetric synthesis. This compound is often employed in the development of drugs targeting neurological disorders, such as antidepressants and antipsychotics, due to its pyrrolidine structure, which is a common motif in CNS-active molecules. Additionally, it serves as a key reagent in the synthesis of natural products and peptidomimetics, where precise stereochemistry is crucial for biological activity. Its role in protecting group chemistry also facilitates the stepwise construction of complex molecules in medicinal chemistry research.

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inventory 50mg
10-20 days ฿6,255.00

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(S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidine
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(S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidine is widely used in organic synthesis, particularly as a chiral building block or intermediate in the production of pharmaceuticals and bioactive compounds. Its silyl-protected hydroxyl group enhances stability and selectivity during complex reactions, making it valuable in asymmetric synthesis. This compound is often employed in the development of drugs targeting neurological disorders, such as antidepressants and antipsychotics, due to its pyrrolidine struc

(S)-3-((tert-Butyldimethylsilyl)oxy)pyrrolidine is widely used in organic synthesis, particularly as a chiral building block or intermediate in the production of pharmaceuticals and bioactive compounds. Its silyl-protected hydroxyl group enhances stability and selectivity during complex reactions, making it valuable in asymmetric synthesis. This compound is often employed in the development of drugs targeting neurological disorders, such as antidepressants and antipsychotics, due to its pyrrolidine structure, which is a common motif in CNS-active molecules. Additionally, it serves as a key reagent in the synthesis of natural products and peptidomimetics, where precise stereochemistry is crucial for biological activity. Its role in protecting group chemistry also facilitates the stepwise construction of complex molecules in medicinal chemistry research.

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