N-Carbobenzoxy-S-benzyl-L-cysteine

98%

  • Product Code: 76570
  CAS:    3257-18-9
Molecular Weight: 345.41 g./mol Molecular Formula: C₁₈H₁₉NO₄S
EC Number: MDL Number: MFCD00004785
Melting Point: 96.0 to 100.0 deg-C Boiling Point:
Density: Storage Condition: Room temperature, sealed, dry
Product Description: This compound is primarily used in peptide synthesis as a protecting group for cysteine residues. The N-carbobenzoxy group protects the amine functionality, while the S-benzyl group safeguards the thiol side chain of cysteine during the synthesis process. This dual protection ensures that the cysteine residue remains intact and unaffected by reactions targeting other parts of the peptide. It is particularly useful in solid-phase peptide synthesis, where selective deprotection steps are required to build complex peptide structures. Additionally, it finds application in the preparation of cysteine-containing peptides for biochemical and pharmaceutical research, enabling the study of peptide interactions, folding, and function.
Product Specification:
Test Specification
APPEARANCE White to Almost white powder to crystal
PURITY 97.5-100
Specific rotation a20DC4EtOH -48.0--44.0
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿2,070.00
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25.000 10-20 days ฿6,750.00
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N-Carbobenzoxy-S-benzyl-L-cysteine
This compound is primarily used in peptide synthesis as a protecting group for cysteine residues. The N-carbobenzoxy group protects the amine functionality, while the S-benzyl group safeguards the thiol side chain of cysteine during the synthesis process. This dual protection ensures that the cysteine residue remains intact and unaffected by reactions targeting other parts of the peptide. It is particularly useful in solid-phase peptide synthesis, where selective deprotection steps are required to build complex peptide structures. Additionally, it finds application in the preparation of cysteine-containing peptides for biochemical and pharmaceutical research, enabling the study of peptide interactions, folding, and function.
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