(S)-1-((S)-1-((S)-1-((S)-1-(tert-Butoxycarbonyl)pyrrolidine-2-carbonyl)pyrrolidine-2-carbonyl)pyrrolidine-2-carbonyl)pyrrolidine-2-carboxylic acid

97%

Reagent Code: #232646
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CAS Number 29804-52-2

science Other reagents with same CAS 29804-52-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 506.59 g/mol
Formula C₂₅H₃₈N₄O₇
badge Registry Numbers
MDL Number MFCD00133644
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of complex peptide-based pharmaceuticals, particularly in the development of protease inhibitors. Its structure allows for sequential coupling in solid-phase peptide synthesis, enabling precise stereochemical control. Commonly employed in the production of antiviral drugs and other bioactive molecules requiring high enantiomeric purity. The tert-butoxycarbonyl (Boc) protecting group facilitates selective deprotection and chain elongation, making it valuable in multi-step syntheses of therapeutic peptides.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,000.00
inventory 250mg
10-20 days ฿16,970.00
inventory 1g
10-20 days ฿45,830.00
(S)-1-((S)-1-((S)-1-((S)-1-(tert-Butoxycarbonyl)pyrrolidine-2-carbonyl)pyrrolidine-2-carbonyl)pyrrolidine-2-carbonyl)pyrrolidine-2-carboxylic acid
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Used as a key intermediate in the synthesis of complex peptide-based pharmaceuticals, particularly in the development of protease inhibitors. Its structure allows for sequential coupling in solid-phase peptide synthesis, enabling precise stereochemical control. Commonly employed in the production of antiviral drugs and other bioactive molecules requiring high enantiomeric purity. The tert-butoxycarbonyl (Boc) protecting group facilitates selective deprotection and chain elongation, making it valuable in

Used as a key intermediate in the synthesis of complex peptide-based pharmaceuticals, particularly in the development of protease inhibitors. Its structure allows for sequential coupling in solid-phase peptide synthesis, enabling precise stereochemical control. Commonly employed in the production of antiviral drugs and other bioactive molecules requiring high enantiomeric purity. The tert-butoxycarbonyl (Boc) protecting group facilitates selective deprotection and chain elongation, making it valuable in multi-step syntheses of therapeutic peptides.

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