(S)-1-Benzyl 2-tert-butyl pyrrolidine-1,2-dicarboxylate

98%

Reagent Code: #236757
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CAS Number 16881-39-3

science Other reagents with same CAS 16881-39-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.37 g/mol
Formula C₁₇H₂₃NO₄
badge Registry Numbers
MDL Number MFCD00051777
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its protected pyrrolidine structure makes it valuable in asymmetric synthesis and peptidomimetic drug design. Commonly employed in the preparation of protease inhibitors and other enzyme-targeted therapeutics. The tert-butyl and benzyl protecting groups allow selective deprotection and functionalization, enabling stepwise construction of complex molecules in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,220.00
inventory 5g
10-20 days ฿7,760.00
inventory 25g
10-20 days ฿31,670.00
(S)-1-Benzyl 2-tert-butyl pyrrolidine-1,2-dicarboxylate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its protected pyrrolidine structure makes it valuable in asymmetric synthesis and peptidomimetic drug design. Commonly employed in the preparation of protease inhibitors and other enzyme-targeted therapeutics. The tert-butyl and benzyl protecting groups allow selective deprotection and functionalization, enabling stepwise constr

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its protected pyrrolidine structure makes it valuable in asymmetric synthesis and peptidomimetic drug design. Commonly employed in the preparation of protease inhibitors and other enzyme-targeted therapeutics. The tert-butyl and benzyl protecting groups allow selective deprotection and functionalization, enabling stepwise construction of complex molecules in medicinal chemistry research.

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