(R)-3-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2,2-dimethylthiazolidine-4-carboxylic Acid
≥97%(HPLC)
- Product Code: 71406
CAS:
873842-06-9
| Molecular Weight: | 383.46 g./mol | Molecular Formula: | C₂₁H₂₁NO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05665145 | |
| Melting Point: | 155 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
This chemical is primarily utilized in peptide synthesis as a protecting group for cysteine residues. The fluorenylmethoxycarbonyl (Fmoc) group shields the thiol functionality during the synthesis process, preventing unwanted side reactions. Its stability under basic conditions makes it particularly useful in solid-phase peptide synthesis, where it can be selectively removed without affecting other protecting groups. The dimethylthiazolidine moiety further enhances the stability of the compound, ensuring efficient and controlled peptide chain elongation. This reagent is essential in producing peptides with high purity and precise sequences, which are critical in pharmaceutical research and drug development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $115.12 |
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(R)-3-[(9H-Fluoren-9-ylmethoxy)carbonyl]-2,2-dimethylthiazolidine-4-carboxylic Acid
This chemical is primarily utilized in peptide synthesis as a protecting group for cysteine residues. The fluorenylmethoxycarbonyl (Fmoc) group shields the thiol functionality during the synthesis process, preventing unwanted side reactions. Its stability under basic conditions makes it particularly useful in solid-phase peptide synthesis, where it can be selectively removed without affecting other protecting groups. The dimethylthiazolidine moiety further enhances the stability of the compound, ensuring efficient and controlled peptide chain elongation. This reagent is essential in producing peptides with high purity and precise sequences, which are critical in pharmaceutical research and drug development.
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