Dimethyl 3,3'-disulfanediyl(2R,2'R)-bis(2-((tert-butoxycarbonyl)amino)propanoate)

97%

Reagent Code: #229555
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CAS Number 77826-55-2

science Other reagents with same CAS 77826-55-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 468.59 g/mol
Formula C₁₈H₃₂N₂O₈S₂
badge Registry Numbers
MDL Number MFCD09757603
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a cross-linking agent in peptide synthesis, particularly for stabilizing peptide structures through disulfide bond formation. Its protected amine groups allow selective deprotection and further functionalization, making it valuable in the preparation of complex peptides and cyclic peptide analogs. Commonly applied in pharmaceutical research for developing bioactive peptides with enhanced stability and conformational control. Also utilized in bioconjugation strategies where controlled dimerization or structural constraint is required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿2,420.00
1g
10-20 days ฿6,510.00
Dimethyl 3,3'-disulfanediyl(2R,2'R)-bis(2-((tert-butoxycarbonyl)amino)propanoate)
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Used as a cross-linking agent in peptide synthesis, particularly for stabilizing peptide structures through disulfide bond formation. Its protected amine groups allow selective deprotection and further functionalization, making it valuable in the preparation of complex peptides and cyclic peptide analogs. Commonly applied in pharmaceutical research for developing bioactive peptides with enhanced stability and conformational control. Also utilized in bioconjugation strategies where controlled dimerization

Used as a cross-linking agent in peptide synthesis, particularly for stabilizing peptide structures through disulfide bond formation. Its protected amine groups allow selective deprotection and further functionalization, making it valuable in the preparation of complex peptides and cyclic peptide analogs. Commonly applied in pharmaceutical research for developing bioactive peptides with enhanced stability and conformational control. Also utilized in bioconjugation strategies where controlled dimerization or structural constraint is required.

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