(2R,2'R)-3,3'-Disulfanediylbis(2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)propanoic acid)

96%

Reagent Code: #53273
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CAS Number 135273-01-7

science Other reagents with same CAS 135273-01-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 684.78 g/mol
Formula C₃₆H₃₂N₂O₈S₂
badge Registry Numbers
MDL Number MFCD00237447
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in peptide synthesis as a protecting group for cysteine residues. The disulfide bond in the molecule helps maintain the structure and stability of peptides during synthesis. It is particularly useful in solid-phase peptide synthesis (SPPS) where controlled deprotection is required. The Fmoc (fluorenylmethoxycarbonyl) group provides temporary protection for the amino group, allowing selective deprotection without affecting other functional groups. This compound is essential in the production of complex peptides and proteins, ensuring high purity and yield in research and pharmaceutical applications.

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Test Parameter Specification
Appearance White Solid
Purity 95.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,800.00
inventory 5g
10-20 days ฿10,880.00
inventory 10g
10-20 days ฿19,800.00

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(2R,2'R)-3,3'-Disulfanediylbis(2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)propanoic acid)
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This chemical is primarily used in peptide synthesis as a protecting group for cysteine residues. The disulfide bond in the molecule helps maintain the structure and stability of peptides during synthesis. It is particularly useful in solid-phase peptide synthesis (SPPS) where controlled deprotection is required. The Fmoc (fluorenylmethoxycarbonyl) group provides temporary protection for the amino group, allowing selective deprotection without affecting other functional groups. This compound is essential

This chemical is primarily used in peptide synthesis as a protecting group for cysteine residues. The disulfide bond in the molecule helps maintain the structure and stability of peptides during synthesis. It is particularly useful in solid-phase peptide synthesis (SPPS) where controlled deprotection is required. The Fmoc (fluorenylmethoxycarbonyl) group provides temporary protection for the amino group, allowing selective deprotection without affecting other functional groups. This compound is essential in the production of complex peptides and proteins, ensuring high purity and yield in research and pharmaceutical applications.

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