(2S,4R)-1-((S)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoyl)-4-hydroxypyrrolidine-2-carboxylic acid

95%

Reagent Code: #36548
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CAS Number 630421-46-4

science Other reagents with same CAS 630421-46-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 344.4000 g/mol
Formula C₁₆H₂₈N₂O₆
badge Registry Numbers
MDL Number MFCD30729679
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of complex peptides and pharmaceutical intermediates. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a hydroxyl group, makes it valuable in peptide chemistry for selective deprotection and coupling reactions. It is often employed in the development of protease inhibitors and other bioactive molecules, particularly in medicinal chemistry research. The chiral centers and functional groups allow for precise control in stereoselective synthesis, making it a key building block in the production of targeted therapeutics. Additionally, its stability and reactivity contribute to its use in solid-phase peptide synthesis (SPPS) for constructing peptide chains with high efficiency and purity.

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Test Parameter Specification
Appearance Off-White Powder
Purity (%) 94.5-100%
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿765.00

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(2S,4R)-1-((S)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoyl)-4-hydroxypyrrolidine-2-carboxylic acid
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This compound is primarily utilized in the synthesis of complex peptides and pharmaceutical intermediates. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a hydroxyl group, makes it valuable in peptide chemistry for selective deprotection and coupling reactions. It is often employed in the development of protease inhibitors and other bioactive molecules, particularly in medicinal chemistry research. The chiral centers and functional groups allow for precise control in stereosele

This compound is primarily utilized in the synthesis of complex peptides and pharmaceutical intermediates. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a hydroxyl group, makes it valuable in peptide chemistry for selective deprotection and coupling reactions. It is often employed in the development of protease inhibitors and other bioactive molecules, particularly in medicinal chemistry research. The chiral centers and functional groups allow for precise control in stereoselective synthesis, making it a key building block in the production of targeted therapeutics. Additionally, its stability and reactivity contribute to its use in solid-phase peptide synthesis (SPPS) for constructing peptide chains with high efficiency and purity.

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