(S)-2-((S)-2-((tert-Butoxycarbonyl)amino)propanamido)-3-methylbutanoic acid

98%

Reagent Code: #232603
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CAS Number 60209-59-8

science Other reagents with same CAS 60209-59-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.34 g/mol
Formula C₁₃H₂₄N₂O₅
badge Registry Numbers
MDL Number MFCD32898809
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of complex peptides and peptidomimetics, particularly in pharmaceutical research for developing enzyme inhibitors and bioactive molecules. Its protected amine group and carboxylic acid functionality allow for selective coupling reactions in solid-phase or solution-phase peptide synthesis. Commonly employed in the preparation of intermediates for drugs targeting metabolic and neurological disorders. The stereochemistry supports high specificity in receptor binding during drug design.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,540.00
inventory 1g
10-20 days ฿4,600.00
inventory 5g
10-20 days ฿16,090.00
(S)-2-((S)-2-((tert-Butoxycarbonyl)amino)propanamido)-3-methylbutanoic acid
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Used as a chiral building block in the synthesis of complex peptides and peptidomimetics, particularly in pharmaceutical research for developing enzyme inhibitors and bioactive molecules. Its protected amine group and carboxylic acid functionality allow for selective coupling reactions in solid-phase or solution-phase peptide synthesis. Commonly employed in the preparation of intermediates for drugs targeting metabolic and neurological disorders. The stereochemistry supports high specificity in receptor

Used as a chiral building block in the synthesis of complex peptides and peptidomimetics, particularly in pharmaceutical research for developing enzyme inhibitors and bioactive molecules. Its protected amine group and carboxylic acid functionality allow for selective coupling reactions in solid-phase or solution-phase peptide synthesis. Commonly employed in the preparation of intermediates for drugs targeting metabolic and neurological disorders. The stereochemistry supports high specificity in receptor binding during drug design.

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