(2S, 4S)-methyl 1-benzyl-4-((tert-butyldimethylsilyl)oxy)pyrrolidine-2-carboxylate

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Reagent Code: #70881
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CAS Number 1318129-60-0

science Other reagents with same CAS 1318129-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 349.54 g/mol
Formula C₁₉H₃₁NO₃Si
badge Registry Numbers
MDL Number MFCD29472562
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a protected hydroxyl group and a carboxylate ester, makes it valuable for constructing chiral pyrrolidine derivatives, which are often found in bioactive compounds and drugs. The tert-butyldimethylsilyl (TBDMS) protecting group ensures selective reactivity during multi-step synthetic processes, allowing chemists to manipulate specific functional groups without interference. Additionally, its chiral centers enable the synthesis of enantiomerically pure compounds, which is crucial in drug development to achieve desired pharmacological effects. This chemical is often employed in the synthesis of antiviral agents, enzyme inhibitors, and other therapeutic molecules targeting various diseases.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,200.00
inventory 250mg
10-20 days ฿11,898.00
inventory 1g
10-20 days ฿23,850.00

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(2S, 4S)-methyl 1-benzyl-4-((tert-butyldimethylsilyl)oxy)pyrrolidine-2-carboxylate
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This compound is primarily utilized in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a protected hydroxyl group and a carboxylate ester, makes it valuable for constructing chiral pyrrolidine derivatives, which are often found in bioactive compounds and drugs. The tert-butyldimethylsilyl (TBDMS) protecting group ensures selective reactivity during multi-step synthetic processes, allowing chemists to ma

This compound is primarily utilized in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. Its structure, featuring a protected hydroxyl group and a carboxylate ester, makes it valuable for constructing chiral pyrrolidine derivatives, which are often found in bioactive compounds and drugs. The tert-butyldimethylsilyl (TBDMS) protecting group ensures selective reactivity during multi-step synthetic processes, allowing chemists to manipulate specific functional groups without interference. Additionally, its chiral centers enable the synthesis of enantiomerically pure compounds, which is crucial in drug development to achieve desired pharmacological effects. This chemical is often employed in the synthesis of antiviral agents, enzyme inhibitors, and other therapeutic molecules targeting various diseases.

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