(R)-2-((tert-butoxycarbonyl)amino)-3-(methyldisulfanyl)propanoic acid

95%

Reagent Code: #229558
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CAS Number 30044-54-3

science Other reagents with same CAS 30044-54-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.372 g/mol
Formula C₉H₁₇NO₄S₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of peptide-based pharmaceuticals, particularly in the development of protease inhibitors. Its protected amine and disulfide-containing side chain make it valuable for constructing complex peptides with defined stereochemistry. Commonly employed in solid-phase peptide synthesis where the Boc group allows for controlled deprotection and chain elongation. The methyldisulfanyl group can be selectively reduced to a thiol for further functionalization or disulfide bond formation, which is critical in mimicking the structure and function of natural bioactive peptides.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿15,440.00
250mg
10-20 days ฿30,880.00
1g
10-20 days ฿74,100.00
(R)-2-((tert-butoxycarbonyl)amino)-3-(methyldisulfanyl)propanoic acid
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Used as a chiral building block in the synthesis of peptide-based pharmaceuticals, particularly in the development of protease inhibitors. Its protected amine and disulfide-containing side chain make it valuable for constructing complex peptides with defined stereochemistry. Commonly employed in solid-phase peptide synthesis where the Boc group allows for controlled deprotection and chain elongation. The methyldisulfanyl group can be selectively reduced to a thiol for further functionalization or disulfi

Used as a chiral building block in the synthesis of peptide-based pharmaceuticals, particularly in the development of protease inhibitors. Its protected amine and disulfide-containing side chain make it valuable for constructing complex peptides with defined stereochemistry. Commonly employed in solid-phase peptide synthesis where the Boc group allows for controlled deprotection and chain elongation. The methyldisulfanyl group can be selectively reduced to a thiol for further functionalization or disulfide bond formation, which is critical in mimicking the structure and function of natural bioactive peptides.

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